Iodobenzene [C6H5I]

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Reaxys ID 1446140 View in Reaxys

1/1 CAS Registry Number: 591-50-4 Chemical Name: iodobenzene; phenyl iodide Linear Structure Formula: (C6H5)I Molecular Formula: C6H5I Molecular Weight: 204.01 Type of Substance: isocyclic InChI Key: SNHMUERNLJLMHN-UHFFFAOYSA-N Note:

I

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Jithendra kumara; Krishnamurthy; Kumara swamy; Shashi kumar; Naik, Satish; Krishna; Naik, Nagaraj; Applied Organometallic Chemistry; vol. 31; nb. 1; (2017); Art.No: E3549, View in Reaxys

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3g

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1i

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7k

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1-4

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2K

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I-40

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F2

Patent; LG Display Co., Ltd.; Lee Seung-jae; Pin Jong-gwan; Lee Bang-suk; Seo Bo-min; (54 pag.); KR2017/79350; (2017); (A) Korean, View in Reaxys

Sub 3-1

Patent; Duksan Neolux Co.,Ltd.; So Gi-ho; Cho Hye-min; Lee Yun-seok; Park Hyeong-geun; Park Jong-gwang; Jeong Yeon-seok; Choi Yeon-hui; Lee Jeong-uk; (66 pag.); KR2017/126400; (2017); (A) Korean, View in Reaxys

Sub 2-1

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Wang, Dingsheng; Chen, Chen; Peng, Qing; Li, Yadong; Chemistry - An Asian Journal; vol. 11; nb. 3; (2016); p. 351 - 355, View in Reaxys II

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11a

Huang, Hsuan-Jui; Lee, Wei-Chih; Yap, Glenn P.A.; Ong, Tiow-Gan; Journal of Organometallic Chemistry; vol.

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2f

Kosobokov, Mikhail D.; Titanyuk, Igor D.; Beletskaya, Irina P.; Tetrahedron Letters; vol. 55; nb. 50; (2014); p. 6791 - 6794, View in Reaxys; Li, Zhijie; Wen, Quan; Zhou, Lihong; Deng, Xingmei; Zeng, Qingle; Synthesis (Germany); vol. 47; nb. 23; (2015); p. 3751 - 3757; Art.No: SS-2015-H0391-OP, View in Reaxys; Lu, Ju-You; Wan, Hong; Zhang, Jianwei; Wang, Zhixuan; Li, Yang; Du, Yongmei; Li, Chunying; Liu, Zhao-Tie; Liu, Zhong-Wen; Lu, Jian; Chemistry - A European Journal; vol. 22; nb. 49; (2016); p. 17542 - 17546, View in Reaxys

III

Soltanzadeh, Bardia; Jaganathan, Arvind; Staples, Richard J.; Borhan, Babak; Angewandte Chemie - International Edition; vol. 54; nb. 33; (2015); p. 9517 - 9522; Angew. Chem.; vol. 127; (2015); p. 9653 - 9658,6, View in Reaxys; Okura, Keisho; Shirakawa, Eiji; European Journal of Organic Chemistry; vol. 2016; nb. 18; (2016); p. 3043 - 3046, View in Reaxys; Patent; Shandong Shenghua Electronic New Material Co., Ltd.; Wu, Shengxi; Du, Kaichang; Wu, Hua; Hou, Juan; Liang, Bin; Sun, Yonghe; Wang, Zuopeng; (12 pag.); CN105348037; (2016); (A) Chinese, View in Reaxys; Patent; Jiaxing University; Yao, Jinzhong; Zhou, Hongwei; He, Jiangjie; Lu, Xiaoyi; Que, Ying; (11 pag.); CN105669486; (2016); (A) Chinese, View in Reaxys

B

Miloserdov, Fedor M.; McKay, David; Muñoz, Bianca K.; Samouei, Hamidreza; MacGregor, Stuart A.; Grushin, Vladimir V.; Angewandte Chemie - International Edition; vol. 54; nb. 29; (2015); p. 8466 - 8470; Angew. Chem.; vol.

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ArX

Wang, Junke; Zong, Yingxiao; Wang, Xicun; Hu, Yulai; Yue, Guoren; Pan, Yi; Green Chemistry; vol. 18; nb. 4; (2016); p. 967 - 973, View in Reaxys

22a

Debnath, Sudarshan; Mondal, Shovan; Synthesis (Germany); vol. 48; nb. 5; (2016); p. 710 - 722, View in Reaxys

1; 14

Gole, Bappaditya; Sanyal, Udishnu; Banerjee, Rahul; Mukherjee, Partha Sarathi; Inorganic Chemistry; vol. 55; nb. 5; (2016); p. 2345 - 2354, View in Reaxys

1'b

Ueno, Ryota; Shimizu, Takashi; Shirakawa, Eiji; Synlett; vol. 27; nb. 5; (2016); p. 741 - 744, View in Reaxys

3d

Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He; Chemical Communications; vol. 52; nb. 31; (2016); p. 5459 - 5462, View in Reaxys

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Xie, Yang; Zhang, Ping; Zhou, Lei; Journal of Organic Chemistry; vol. 81; nb. 5; (2016); p. 2128 - 2134, View in Reaxys

2a'

Yamaguchi, Miyuki; Higuchi, Mayu; Tazawa, Kanae; Manabe, Kei; Journal of Organic Chemistry; vol. 81; nb. 9; (2016); p. 3967 - 3974, View in Reaxys

6a-I

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8c

Singh, Gurpreet; Kumar, Manoj; Sharma, Kamaldeep; Bhalla, Vandana; Green Chemistry; vol. 18; nb. 11; (2016); p. 3278 - 3285, View in Reaxys

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6(1)

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2t

Liu, Xi-Hai; Leng, Jing; Jia, Su-Jiao; Hao, Jian-Hong; Zhang, Fanglin; Qin, Hua-Li; Zhang, Cheng-Pan; Journal of Fluorine Chemistry; vol. 189; (2016); p. 59 - 67, View in Reaxys

4j

Qi, Chaorong; Hu, Xiaohan; He, Haitao; Synlett; vol. 27; nb. 13; (2016); p. 1979 - 1982; Art.No: ST-2016-W0122-L, View in Reaxys

1''

Han, Qingshuai; Fu, Shurong; Zhang, Xiaofeng; Lin, Shen; Huang, Qiufeng; Tetrahedron Letters; vol. 57; nb. 37; (2016); p. 4165 - 4169, View in Reaxys

S-7

Xu, Qiu-Qin; Hou, Qi-Lan; Liu, Wei; Wang, Hai-Jing; Liao, Wei-Wei; Organic Letters; vol. 18; nb. 15; (2016); p.

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Sub 1-2-1; Sub 6-3-5; Sub 6-4-5

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Ar%1&1

Prabagar; Nayak, Sanatan; Prasad, Rangu; Sahoo, Akhila K.; Organic Letters; vol. 18; nb. 13; (2016); p. 3066 3069, View in Reaxys

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S-3

Wang, Xiangbo; Zhou, Yunfei; Qiu, Lihua; Yao, Ruwei; Zheng, Yang; Zhang, Cheng; Bao, Xiaoguang; Xu, Xinfang; Advanced Synthesis and Catalysis; vol. 358; nb. 10; (2016); p. 1571 - 1576, View in Reaxys

2a; 2c

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S1a

Xu, Bin; Tambar, Uttam K.; Journal of the American Chemical Society; vol. 138; nb. 37; (2016); p. 12073 - 12076, View in Reaxys

12b

Mondal, Biplab; Roy, Brindaban; Kazmaier, Uli; Journal of Organic Chemistry; vol. 81; nb. 23; (2016); p. 11646 11655, View in Reaxys

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S8

Guo, Lin; Rueping, Magnus; Chemistry - A European Journal; vol. 22; nb. 47; (2016); p. 16787 - 16790, View in Reaxys

4q

Jerhaoui, Soufyan; Chahdoura, Faouzi; Rose, Clémence; Djukic, Jean-Pierre; Wencel-Delord, Joanna; Colobert, Françoise; Chemistry - A European Journal; vol. 22; nb. 48; (2016); p. 17397 - 17406, View in Reaxys

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Patent; KAINOS MEDICINE, INC.; CHOI, Minjeong; OH, Su-Sung; (113 pag.); WO2016/186453; (2016); (A1) English, View in Reaxys

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1l'

Gu, Liuqun; Lu, Ting; Zhang, Mingyun; Tou, Lijuan; Zhang, Yugen; Advanced Synthesis and Catalysis; vol. 355; nb. 6; (2013); p. 1077 - 1082, View in Reaxys

2a, PhI

Davis, Owen A.; Hughes, Matthew; Bull, James A.; Journal of Organic Chemistry; vol. 78; nb. 7; (2013); p. 3470 3475, View in Reaxys

8; 2a; 2f

Jacquemot, Guillaume; Menard, Marc-Andre; L'Homme, Chloe; Canesi, Sylvain; Chemical Science; vol. 4; nb. 3; (2013); p. 1287 - 1292, View in Reaxys

S2

Zhang, Jing; Ugrinov, Angel; Zhao, Pinjing; Angewandte Chemie - International Edition; vol. 52; nb. 26; (2013); p.

6681 - 6684; Angew. Chem.; vol. 125; nb. 26; (2013); p. 6813 - 6816,4, View in Reaxys

5h

Groll, Klaus; Manolikakes, Sophia M.; Du Jourdin, Xavier Mollat; Jaric, Milica; Bredihhin, Aleksei; Karaghiosoff, Konstantin; Carell, Thomas; Knochel, Paul; Angewandte Chemie - International Edition; vol. 52; nb. 26; (2013); p. 6776 - 6780; Angew. Chem.; (2013); p. 6909 - 6913, View in Reaxys

30b

Heinrich, Annika C. J.; Thiedemann, Birk; Gates, Paul J.; Staubitz, Anne; Organic Letters; vol. 15; nb. 18; (2013); p. 4666 - 4669, View in Reaxys

b9

Gurung, Santosh K.; Thapa, Surendra; Vangala, Adarsh S.; Giri, Ramesh; Organic Letters; vol. 15; nb. 20; (2013); p. 5378 - 5381, View in Reaxys

2a; 1b

Huang, Zhongxing; Dong, Guangbin; Journal of the American Chemical Society; vol. 135; nb. 47; (2013); p. 17747 17750, View in Reaxys

16

Elliott, Emma-Claire; Maggs, James L.; Park, B. Kevin; O'Neill, Paul M.; Stachulski, Andrew V.; Organic and Biomolecular Chemistry; vol. 11; nb. 48; (2013); p. 8426 - 8434, View in Reaxys

1s

Chen, Guangwei; Leng, Yuting; Yang, Fan; Wang, Shiwei; Wu, Yangjie; Chinese Journal of Chemistry; vol. 31; nb.

12; (2013); p. 1488 - 1494, View in Reaxys

13b

Parella, Ramarao; Gopalakrishnan, Bojan; Babu, Srinivasarao Arulananda; Journal of Organic Chemistry; vol. 78; nb. 23; (2013); p. 11911 - 11934, View in Reaxys

1m

Dong, Zhe; Dong, Guangbin; Journal of the American Chemical Society; vol. 135; nb. 49; (2013); p. 18350 - 18353, View in Reaxys

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24

Chahdoura, Faouzi; Pradel, Christian; Gomez, Montserrat; Advanced Synthesis and Catalysis; vol. 355; nb. 18; (2013); p. 3648 - 3660, View in Reaxys

54

Bourbeau, Matthew P.; Siegmund, Aaron; Allen, John G.; Shu, Hong; Fotsch, Christopher; Bartberger, Michael D.; Kim, Ki-Won; Komorowski, Renee; Graham, Melissa; Busby, James; Wang, Minghan; Meyer, James; Xu, Yang; Salyers, Kevin; Fielden, Mark; Veniant, Murielle M.; Gu, Wei; Journal of Medicinal Chemistry; vol. 56; nb.

24; (2013); p. 10132 - 10141, View in Reaxys

3i

Hoshiya, Naoyuki; Kobayashi, Takaaki; Arisawa, Mitsuhiro; Shuto, Satoshi; Organic Letters; vol. 15; nb. 24; (2013); p. 6202 - 6205, View in Reaxys

112

Patent; DUKE UNIVERSITY; ZHOU, Pei; TOONE, Eric, J.; WO2012/31298; (2012); (A2) English, View in Reaxys

Compound 1h; 1h

Patent; Amii, Hideki; Fujikawa, Kenichi; Fujioka, Yasutaka; Matsuura, Makoto; US2012/220795; (2012); (A1) English, View in Reaxys

T-1,E-1-3-Sm

Keles, Mustafa; Yilmaz, Mustafa Kemal; Heteroatom Chemistry; vol. 23; nb. 5; (2012); p. 466 - 471, View in Reaxys

12e

Izgu, Enver Cagri; Hoye, Thomas R.; Tetrahedron Letters; vol. 53; nb. 37; (2012); p. 4938 - 4941, View in Reaxys

36a

O'Rourke, Natasha F.; Davies, Katherine A.; Wulff, Jeremy E.; Journal of Organic Chemistry; vol. 77; nb. 19; (2012); p. 8634 - 8647,14, View in Reaxys; O'Rourke, Natasha F.; Davies, Katherine A.; Wulff, Jeremy E.; Journal of Organic Chemistry; vol. 77; nb. 19; (2012); p. 8634 - 8647, View in Reaxys

5g

Grigg, Ronald; Elboray, Elghareeb E.; Aly, Moustafa F.; Abbas-Temirek, Hussien H.; Chemical Communications (Cambridge, United Kingdom); vol. 48; nb. 94; (2012); p. 11504 - 11506,3, View in Reaxys

5e

Brachet, Etienne; Messaoudi, Samir; Peyrat, Jean-Franaois; Brion, Jean-Daniel; Alami, Mouad; Advanced Synthesis and Catalysis; vol. 354; nb. 14-15; (2012); p. 2829 - 2839,11, View in Reaxys; Brachet, Etienne; Messaoudi, Samir; Peyrat, Jean-Franaois; Brion, Jean-Daniel; Alami, Mouad; Advanced Synthesis and Catalysis; vol. 354; nb.

14-15; (2012); p. 2829 - 2839, View in Reaxys

5c; PhI

Bagley, Mark C.; Fusillo, Vincenzo; Hills, Edward G.B.; Mulholland, Alex T.; Newcombe, Joseph; Pentecost, Leanne J.; Radley, Emily L.; Stephens, Bethan R.; Turrell, Christopher C.; Arkivoc; vol. 2012; nb. 7; (2012); p. 294 - 313, View in Reaxys

1,5

Soleiman-Beigi, Mohammad; Mohammadi, Fariba; Tetrahedron Letters; vol. 53; nb. 52; (2012); p. 7028 - 7030, View in Reaxys

4; PhI

Chen, Yu; Dubrovskiy, Anton; Larock, Richard C.; Organic Syntheses; vol. 89; (2012); p. 294 - 306, View in Reaxys

8-F

Patent; Rutgers, The State University of New Jersey; US8008528; (2011); (B2) English, View in Reaxys

Table 2, entry 1

Hossain, Md. Delwar; Oyamada, Juzo; Kitamura, Tsugio; Synthesis; nb. 5; (2008); p. 690 - 692, View in Reaxys

13

Hastings, Courtney J.; Pluth, Michael D.; Biros, Shannon M.; Bergman, Robert G.; Raymond, Kenneth N.; Tetrahedron; vol. 64; nb. 36; (2008); p. 8362 - 8367, View in Reaxys

title comp.

Keefe, C. Dale; Butler, Ellen; Gillis, Elizabeth; MacDonald, Jennifer L.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 1; (2007); p. 125 - 138, View in Reaxys

Table 1. aryl halide

Hong, Chang Sung; Seo, Jae Young; Yum, Eul Kgun; Tetrahedron Letters; vol. 48; nb. 28; (2007); p. 4831 - 4833, View in Reaxys

starting to 5

Nakagawa, Kojiro; Tomita, Ikuyoshi; Chemistry Letters; vol. 36; nb. 5; (2007); p. 638 - 639, View in Reaxys

Substr.,Tab.4,run13/11

Altava, Belen; Burguete, M. Isabel; Garcia-Verdugo, Eduardo; Karbass, Naima; Luis, Santiago V.; Puzary, Amrit; Sans, Victor; Tetrahedron Letters; vol. 47; nb. 14; (2006); p. 2311 - 2314, View in Reaxys

Tab. 1, entry 18

Chiappe, Cinzia; Pieraccini, Daniela; Zhao, Dongbin; Fei, Zhaofu; Dyson, Paul J.; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 68 - 74, View in Reaxys

Tab. 2, entry 2

Consorti, Crestina S.; Flores, Fabricio R.; Rominger, Frank; Dupont, Jairton; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 133 - 141, View in Reaxys

1a, Tab. 1, entry 4

Cwik, Agnieszka; Hell, Zoltan; Figueras, Francois; Advanced Synthesis and Catalysis; vol. 348; nb. 4-5; (2006); p.

523 - 530, View in Reaxys

Tab. 1

Zawartka; Trzeciak; Ziolkowski; Lis; Ciunik; Pernak; Advanced Synthesis and Catalysis; vol. 348; nb. 12-13; (2006); p. 1689 - 1698, View in Reaxys; Sathiyapriya; Karunakaran, R. Joel; Journal of Chemical Research; nb. 9; (2006); p. 575 - 576, View in Reaxys

1a, Figure 3

Pachon, Laura Duran; Elsevier, Cornells J.; Rothenberg, Gadi; Advanced Synthesis and Catalysis; vol. 348; nb.

12-13; (2006); p. 1705 - 1710, View in Reaxys

table 2, 39

Abraham, Raymond J.; Byrne, Jonathan J.; Griffiths, Lee; Perez, Manuel; Magnetic Resonance in Chemistry; vol.

44; nb. 5; (2006); p. 491 - 509, View in Reaxys

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iodobenzene

Ambulgekar, Girish V.; Bhanage, Bhalchandra M.; Samant, Shriniwas D.; Tetrahedron Letters; vol. 46; nb. 14; (2005); p. 2483 - 2485, View in Reaxys

9, Ar=Ph

Thompson, Alicia L. S.; Kabalka, George W.; Akula, Murthy R.; Huffman, John W.; Synthesis; nb. 4; (2005); p.

547 - 550; Art.No: M05304SS, View in Reaxys

Tab 1 Entry 1

Papp, Attila; Galbacs, Gabor; Molnar, Arpad; Tetrahedron Letters; vol. 46; nb. 45; (2005); p. 7725 - 7728, View in Reaxys

PHI

Sun, Wei; Herdtweck, Eberhardt; Kuehn, Fritz E.; New Journal of Chemistry; vol. 29; nb. 12; (2005); p. 1577 1580, View in Reaxys

entry 7

Firouzabadi, Habib; Iranpoor, Nasser; Garzan, Atefeh; Advanced Synthesis and Catalysis; vol. 347; nb. 15; (2005); p. 1925 - 1928, View in Reaxys

12

Buback, Michael; Perkovic, Thomas; Redlich, Stefan; De Meijere, Armin; European Journal of Organic Chemistry; nb. 13; (2003); p. 2375 - 2382, View in Reaxys; Patent; Kyocera Mita Corporation (Mita Industry Co., Ltd.; JP2005/82586; (2005); (A) Japanese, View in Reaxys

23

Patent; Kyocera Mita Corporation; JP2005/200358; (2005); (A) Japanese, View in Reaxys

32

Patent; Kyocera Mita Corporation; JP2005/213183; (2005); (A) Japanese, View in Reaxys

tab.3, entry 1, ArI

Agou, Tomohiro; Kobayashi, Junji; Kawashima, Takayuki; Chemistry Letters; vol. 33; nb. 8; (2004); p. 1028 - 1029, View in Reaxys

7a, Tab. 1, entry 3

Takenaka, Kazuhiro; Uozumi, Yasuhiro; Advanced Synthesis and Catalysis; vol. 346; nb. 13-15; (2004); p. 1693 1696, View in Reaxys

Product, Tab.2, run 1

Kabalka, George W.; Mereddy, Arjun R.; Tetrahedron Letters; vol. 45; nb. 2; (2004); p. 343 - 345, View in Reaxys

1a, Tab. 1, entry 8

Kmentova, Iveta; Gotov, Battsengel; Gajda, Vladimir; Toma, Stefan; Monatshefte fur Chemie; vol. 134; nb. 4; (2003); p. 545 - 549, View in Reaxys

prod. Tab. 1, entry 11

Alexander, Varughese M.; Khandekar, Amit C.; Samant, Shriniwas D.; Synlett; nb. 12; (2003); p. 1895 - 1897, View in Reaxys

prod., Tab. 2, entry 6

Firouzabadi; Iranpoor; Shiri; Tetrahedron Letters; vol. 44; nb. 49; (2003); p. 8781 - 8785, View in Reaxys

p. 933

Tanemura, Kiyoshi; Suzuki, Tsuneo; Nishida, Yoko; Satsumabayashi, Koko; Horaguchi, Takaaki; Chemistry Letters; vol. 32; nb. 10; (2003); p. 932 - 933, View in Reaxys

Table 1, col 1, run 1-3

Dell'Anna, Maria M.; Mastrorilli, Piero; Muscio, Francesco; Nobile, Cosimo F.; Suranna, Gian P.; European Journal of Inorganic Chemistry; nb. 5; (2002); p. 1094 - 1099, View in Reaxys

Tab.2

Venkatraman, Sripathy; Huang, Taisheng; Li, Chao-Jun; Advanced Synthesis and Catalysis; vol. 344; nb. 3-4; (2002); p. 399 - 405, View in Reaxys

xv

Patent; E.I. DU PONT DE NEMOURS AND COMPANY; EP1178040; (2002); (A1) English, View in Reaxys

32a

Patent; Sony Corporation; US6337167; (2002); (B1) English, View in Reaxys

3, Tab.1., run 1.

Patrick, Timothy B.; Juehne, Thomas; Reeb, Elmer; Hennessy, Daniel; Tetrahedron Letters; vol. 42; nb. 21; (2001); p. 3553 - 3554, View in Reaxys

1, R=H

Hagiwara, Hisahiro; Shimizu, Yumiko; Hoshi, Takashi; Suzuki, Toshio; Ando, Masayoshi; Ohkubo, Keisuke; Yokoyama, Chiaki; Tetrahedron Letters; vol. 42; nb. 26; (2001); p. 4349 - 4351, View in Reaxys

11b

Chaikovski; Filimonov; Yagovkin; Ogorodnikov; Russian Chemical Bulletin; vol. 50; nb. 12; (2001); p. 2411 - 2415, View in Reaxys

3h

Lormann, Matthias; Dahmen, Stefan; Braese, Stefan; Tetrahedron Letters; vol. 41; nb. 20; (2000); p. 3813 - 3816, View in Reaxys

65

Bel'skii; Russian Chemical Bulletin; vol. 49; nb. 2; (2000); p. 251 - 255, View in Reaxys

PhX, X=I

Mukhopadhyay, Sudip; Rothenberg, Gadi; Gitis, Diana; Baidossi, Mubeen; Ponde, Datta E.; Sasson, Yoel; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2000); p. 1809 - 1812, View in Reaxys

col1,run1,3,5,7,9,11 Varma, Rajender S.; Naicker, Kannan P.; Tetrahedron Letters; vol. 40; nb. 3; (1999); p. 439 - 442, View in Reaxys ,13 PhI (Tab.1,run 1,col Buynak, John D.; Doppalapudi, Venkata Ramana; Frotan, Mohammed; Kumar, Ramon; Tetrahedron Letters; vol.

1) 40; nb. 7; (1999); p. 1281 - 1284, View in Reaxys Fig 1, Tab 1, substrate

Bhanage, Bhalchandra M.; Ikushima, Yutaka; Shirai, Masayuki; Arai, Masahiko; Tetrahedron Letters; vol. 40; nb.

35; (1999); p. 6427 - 6430, View in Reaxys

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R'X, X=I, R'=Ph

Bandini, Marco; Cozzi, Pier Giorgio; Umani-Ronchi, Achille; Villa, Marzia; Tetrahedron; vol. 55; nb. 26; (1999); p.

8103 - 8110, View in Reaxys

educt to 6a

Sauer, Juergen; Heldmann, Dieter K.; Tetrahedron Letters; vol. 39; nb. 17; (1998); p. 2549 - 2552, View in Reaxys

C6H6I

Zhong, Dongping; Zewail, Ahmed H.; Journal of Physical Chemistry A; vol. 102; nb. 23; (1998); p. 4031 - 4058, View in Reaxys

17

Liu; Wang; Chen; Li; Yu; Bulletin of Environmental Contamination and Toxicology; vol. 57; nb. 3; (1996); p. 421 425, View in Reaxys

Patent-Specific Data (67) Prophetic ComLocation in Patent pound

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Janssen Pharmaceutica NV; Alcazar Vaca, Manuel Jesus; Andres Gil, Jose Ignacio; Chrovian, Christa C.; Coate, Heather R.; De Angelis, Meri; Dvorak, Curt A.; Gelin, Christine F.; Letavic, Michael A.; Savall, Brad M.; Soyode-Johnson, Akinola; Stenne, Brice M.; Swanson, Devin M.; US2014/275015; (2014); (A1) English, View in Reaxys; Patent; ABT Holding Company; Robarge, Michael; Zawadski, Michelle; Harrington, John; US2014/275035; (2014); (A1) English, View in Reaxys; Patent; Tsuboi, Katsunori; Takanashi, Yosuke; Tojo, Shingo; Kodama, Tomohiro; Kubota, Katsumi; Kanai, Toshio; US2014/275076; (2014); (A1) English, View in Reaxys; Patent; Takeda Pharmaceutical Company Limited; KUSUMOTO, Tomokazu; SASAKI, Shigekazu; MAEZAKI, Hironobu; EP2824106; (2015); (A1) English, View in Reaxys; Patent; Takeda Pharmaceutical Company Limited; NARA, Hiroshi; DAINI, Masaki; KAIEDA, Akira; KAMEI, Taku; IMAEDA, Toshihiro; KIKUCHI, Fumiaki; EP2857400; (2015); (A1) English, View in Reaxys; Patent; Acetylon Pharmaceuticals, Inc.; Jones, Simon Stewart; Yang, Min; Tamang, David Lee; US2015/105384; (2015); (A1) English, View in Reaxys; Patent; ONO Pharmaceutical Co., Ltd.; ISHIDA, Akiharu; MATSUSHITA, Takeshi; SEKIGUCHI, Tetsuya; KOMAGATA, Tatsuya; NISHIO, Takuya; EP2871179; (2015); (A1) English, View in Reaxys; Patent; Hodogaya Chemical Co., Ltd.; YOKOYAMA, Norimasa; KANDA, Daizou; HAYASHI, Shuichi; EP2894155; (2015); (A1) English, View in Reaxys Patent; Sanofi; Baku, Eritsuku; Bulolo, Morice; Cross, Annie; El Amado, Youssef; Fuiroshiyu, Lom Brunnow; Array, Frank; Carlson, Carl Andreas; Marciniak, Gilbert; Ronan, Baptiste; Shio, Laulan; Bibe, Bertrand; Viviani, Fabrice; Zimerman, Andre; (90 pag.); JP5655070; (2015); (B2) Japanese, View in Reaxys Patent; Cheil Industries Co.,Ltd; Lee, Han Ir; Yoo, Eun Sun; Kang, Dong Min; Sin, Ji Hun; Yoo, Dong Kyu; Lee, Sang Sin; Jang, Yoo Na; Jung, Soo Young; Han, Su Jin; Hong, Jin Suk; (46 pag.); KR2015/24669; (2015); (A) Korean, View in Reaxys Patent; Nagoya Institute of Technology; Shibata, Tetsuo; Suzuki, Satoru; Kamo, Tomohiro; Hiramatsu, Takaaki; (12 pag.); JP2015/63500; (2015); (A) Japanese, View in Reaxys Patent; UNIVERSITE LAVAL; CORMIER, Yvon; ISRAEL ASSAYAG, Evelyne; LAVALLÉE, Pierre; WO2014/71512; (2014); (A1) English, View in Reaxys Page/Page column

Patent; Takeda Pharmaceutical Company Limited; TOYOFUKU, Masashi; NAKAMURA, Shinji; HONDA, Eiji; EP2813508; (2014); (A1) English, View in Reaxys Patent; SDS Biotech K.K.; Sakai, Masaaki; Matsumura, Tomoaki; Midorikawa, Satohiro; Nomoto, Takashi; Muraki, Tomoko; Katsuki, Ryutaro; US2013/296271; (2013); (A1) English, View in Reaxys Patent; SDS Biotech K. K.; EP2455371; (2012); (A1) English, View in Reaxys Patent; Taillefer, Marc; Tlilli, Anis; Monnier, Florian; Xia, Ning; US2012/157704; (2012); (A1) English, View in Reaxys Patent; BIOGEN IDEC MA INC.; SUNESIS PHARMACEUTICALS, INC.; BUI, Minna; CONLON, Patrick; ERLANSON, Daniel, A.; FAN, Junfa; GUAN, Bing; HOPKINS, Brian, T.; ISHCHENKO, Alexey; JENKINS, Tracy, J.; KUMARAVEL, Gnanasambandam; MARCOTTE, Doug; POWELL, Noel; SCOTT, Daniel; TAVERAS, Art; WANG, Deping; ZHONG, Min; WO2011/29043; (2011); (A1) English, View in Reaxys Patent; Bahmanyar, Sogole; Bates, R.J.; Blease, Kate; Calabrese, Andrew Antony; Daniel, Thomas Oran; Delgado, Mercedes; Elsner, Jan; Erdman, Paul; Fahr, Bruce; Ferguson, Gregory; Lee, Branden; Nadolny, Lisa; Packard, Garrick; Papa, Patrick; Plantevin-Krenitsky, Veronique; Riggs, Jennifer; Rohane, Patricia; Sankar, Sabita; Sapienza, John; Satoh, Yoshitaka; Sloan, Victor; Stevens, Randall; Tehrani, Lida; Tikhe, Jayashree; Torres, Eduardo; Wallace, Andrew; Whitefield, Brandon Wade; Zhao, Jingjing; US2010/93698; (2010); (A1) English, View in Reaxys Patent; SUMITOMO CHEMICAL COMPANY, LIMITED; GENENTECH, INC.; MIKI, Takashi; SHIMASAKI, Yasuharu; BABU, Srinivasan; CHENG, Zhigang; REYNOLDS, Mark, E.; TIAN, Qingping; WO2010/110782; (2010); (A1) English, View in Reaxys Patent; SCHERING CORPORATION; PTC THERAPEUTICS, INC; MACCOSS, Malcolm; NJOROGE, F., George; NOMEIR, Amin; CHEN, Guangming; KARP, Gary, Mitchell; LENNOX, William, Joseph; LI, Chunshi; MORRILL, Christie; PAGET, Steven, D.; REN, Hongyu; ZHANG, Nanjing; ZHANG, Xiaoyan; WO2010/117935; (2010); (A1) English, View in Reaxys Patent; Taillefer, Marc; Xia, Ning; US2010/298571; (2010); (A1) English, View in Reaxys Patent; CONCERT PHARMACEUTICALS, INC.; WO2009/35598; (2009); (A1) English, View in Reaxys

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Patent; University of Ottawa; US2008/132698; (2008); (A1) English, View in Reaxys Patent; IRM LLC; THE SCRIPPS RESEARCH INSTITUTE; WO2008/94737; (2008); (A2) English, View in Reaxys Patent; AUSPEX PHARMACEUTICALS, INC.; US2008/319026; (2008); (A1) English, View in Reaxys prophetic product

Patent; Hiratsuka, Atsunori; Yano, Kazuyoshi; Karube, Isao; Tsai, Shuo-Wen; Yokoyama, Kenji; Koide, Satoshi; Akimoto, Takuo; US2006/113189; (2006); (A1) English, View in Reaxys Patent; DAIICHI PHARMACEUTICAL CO., LTD.; WO2006/13939; (2006); (A1) Japanese, View in Reaxys Patent; AMERSHAM PLC; WO2005/42441; (2005); (A1) English, View in Reaxys Patent; COUNCIL OF SCIENTIFIC and INDUSTRIAL RESEARCH; WO2005/63680; (2005); (A1) English, View in Reaxys Patent; ASTRAZENECA AB; WO2005/3123; (2005); (A1) English, View in Reaxys Patent; Sumitomo Chemical Co., Ltd; JP2005/8578; (2005); (A) Japanese, View in Reaxys Patent; IRM LLC; US2005/124637; (2005); (A1) English, View in Reaxys Patent; NIKEM RESEARCH S.R.L.; WO2004/85438; (2004); (A2) English, View in Reaxys Patent; MEMORY PHARMACEUTICALS CORPORATION; WO2004/9552; (2004); (A1) English, View in Reaxys Patent; MASSACHUSETTS INSTITUTE OF TECHNOLOGY; WO2004/13094; (2004); (A2) English, View in Reaxys Patent; ASTRAZENECA AB; WO2004/52880; (2004); (A1) English, View in Reaxys Patent; Cellier, Pascal Philippe; Cristau, Henri-Jean; Spindler, Jean-Francis; Taillefer, Marc; US2003/236413; (2003); (A1) English, View in Reaxys Patent; E.I. DU PONT DE NEMOURS AND COMPANY; EP1178040; (2002); (A1) English, View in Reaxys

prophetic product

Patent; Takasago International Corporation; US6365776; (2002); (B1) English, View in Reaxys Patent; Sony Corporation; US6337167; (2002); (B1) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

3.09

H Bond Donors

0

H Bond Acceptors

0

Rotatable Bonds

0

TPSA

0

Lipinski Number

4

Veber Number

2

Catalyst Investigation (16) 1 of 16

Investigated characteristic(s)

Catalytic activity

Specification of catalysis

Regioselective catalysis

Liang, Dongdong; Sersen, Deanna; Yang, Chao; Deschamps, Jeffrey R.; Imler, Gregory H.; Jiang, Chao; Xue, Fengtian; Organic and Biomolecular Chemistry; vol. 15; nb. 20; (2017); p. 4390 - 4398, View in Reaxys 2 of 16

Investigated characteristic(s)

Catalytic activity; Diastereomeric excess

Specification of catalysis

Regioselective catalysis; Stereoselective catalysis

Banik, Steven M.; Mennie, Katrina M.; Jacobsen, Eric N.; Journal of the American Chemical Society; vol. 139; nb. 27; (2017); p. 9152 - 9155, View in Reaxys 3 of 16

Investigated characteristic(s)

Catalytic activity

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Type of reaction (Catalyst Investigation)

Cycloisomerization

Location

supporting information

Co-catalyst/co-substrate name

3-chloro-benzenecarboperoxoic acid

Okamura, Yuki; Sato, Daisuke; Yoshimura, Akira; Zhdankin, Viktor V.; Saito, Akio; Advanced Synthesis and Catalysis; vol. 359; nb. 18; (2017); p. 3243 - 3247, View in Reaxys 4 of 16

Investigated characteristic(s)

Catalytic activity

Specification of catalysis

Phase-transfer catalysis

Type of reaction (Catalyst Investigation)

Cycloisomerization

Location

supporting information

Co-catalyst/co-substrate name

Oxone; tetra(n-butyl)ammonium hydrogensulfate

Okamura, Yuki; Sato, Daisuke; Yoshimura, Akira; Zhdankin, Viktor V.; Saito, Akio; Advanced Synthesis and Catalysis; vol. 359; nb. 18; (2017); p. 3243 - 3247, View in Reaxys 5 of 16

Investigated characteristic(s)

Catalytic activity

Shen, Chao; Yang, Ming; Xu, Jun; Chen, Chao; Zheng, Kai; Shen, Jiabing; Zhang, Pengfei; RSC Advances; vol. 7; nb. 78; (2017); p. 49436 - 49439, View in Reaxys 6 of 16

Investigated characteristic(s)

Catalytic activity; Diastereomeric excess

Specification of catalysis

Stereoselective catalysis

Wang, Shuo-En; He, Qiuqin; Fan, Renhua; Organic Letters; vol. 19; nb. 24; (2017); p. 6478 - 6481, View in Reaxys 7 of 16

Investigated characteristic(s)

Catalytic activity

Location

Paragraph 0037-0051

Patent; Saga University; Tosoh F-Tech Co., Ltd.; Kitamura, Tsugio; Kagawa, Takumi; (52 pag.); JP5959467; (2016); (B2) Japanese, View in Reaxys 8 of 16

Investigated characteristic(s)

Enantiomeric excess; Catalytic activity

Specification of catalysis

Stereoselective catalysis

Co-catalyst/co-substrate name

3-chloro-benzenecarboperoxoic acid

Basdevant, Benoit; Legault, Claude Y.; Organic Letters; vol. 17; nb. 19; (2015); p. 4918 - 4921, View in Reaxys 9 of 16

Investigated characteristic(s)

Catalytic activity

Specification of catalysis

Chemoselective catalysis

Type of reaction (Catalyst Investigation)

Halogenation

Location

supporting information

Stodulski, Maciej; Goetzinger, Alissa; Kohlhepp, Stefanie V.; Gulder, Tanja; Chemical Communications; vol. 50; nb. 26; (2014); p. 3435 - 3438, View in Reaxys 10 of 16

Investigated characteristic(s)

Catalytic activity

Type of reaction (Catalyst Investigation)

Cycloaddition

Co-catalyst/co-substrate name

3-chloro-benzenecarboperoxoic acid

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Xiang, Changbin; Li, Tingting; Yan, Jie; Synthetic Communications; vol. 44; nb. 5; (2014); p. 682 - 688, View in Reaxys 11 of 16

Investigated characteristic(s)

Catalytic activity

Type of reaction (Catalyst Investigation)

Cyclization

Co-catalyst/co-substrate name

3-chloro-benzenecarboperoxoic acid; potassium bromide

Li, Tingting; Xiang, Changbin; Zhang, Bijun; Yan, Jie; Helvetica Chimica Acta; vol. 97; nb. 6; (2014); p. 854 - 860, View in Reaxys 12 of 16

Investigated characteristic(s)

Catalytic activity; Mechanism of catalysis

Specification of catalysis

Regioselective catalysis

Type of reaction (Catalyst Investigation)

Annulation

Location

supporting information

Co-catalyst/co-substrate name

peracetic acid

Manna, Srimanta; Antonchick, Andrey P.; Angewandte Chemie - International Edition; vol. 53; nb. 28; (2014); p. 7324 7327; Angew. Chem.; vol. 126; nb. 28; (2014); p. 7452 - 7455,4, View in Reaxys 13 of 16

Investigated characteristic(s)

Catalyst activation

Type of reaction (Catalyst Investigation)

Cyclization

Location

supporting information

Co-catalyst/co-substrate name

Selectfluor

Fra, Laura; Millán, Alba; Souto, José A.; Muñiz, Kilian; Angewandte Chemie - International Edition; vol. 53; nb. 28; (2014); p. 7349 - 7353, View in Reaxys 14 of 16

Investigated characteristic(s)

Catalytic activity

Type of reaction (Catalyst Investigation)

Amination

Yan, Yizhe; Zhang, Yonghui; Zha, Zhenggen; Wang, Zhiyong; Organic Letters; vol. 15; nb. 9; (2013); p. 2274 - 2277, View in Reaxys 15 of 16

Investigated characteristic(s)

Mechanism of catalysis

Type of reaction (Catalyst Investigation)

Oxidative cleavage

Jia, Xiao-Chuan; Li, Jing; Yu, Zhi-Rui; Wang, Yu-Hu; Zhou, Lei; Yu, Yan-Yan; Journal of Chemical Research; vol. 37; nb.

7; (2013); p. 420 - 421, View in Reaxys 16 of 16

Investigated characteristic(s)

Catalytic activity

Specification of catalysis

Regioselective catalysis

Type of reaction (Catalyst Investigation)

Chlorination

Co-catalyst/co-substrate name

toluene-4-sulfonic acid

Li, Ting-Ting; Xu, Cui; Xiang, Chang-Bin; Yan, Jie; Chinese Chemical Letters; vol. 24; nb. 6; (2013); p. 535 - 538, View in Reaxys Derivative (20) Comment (Derivative)

Derivative

References

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(Dichloroiodo)benzene

Weiss, Robert; Wagner, Klaus-Georg; Chemische Berichte; vol. 117; nb. 5; (1984); p. 1973 1976, View in Reaxys

TCNE-Komplex : Abs.Sp.

Bendig; Kreysig; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 258; (1977); p. 1176, View in Reaxys

Bld.-geschw.-Jodkomplex in CCl4

Clark; Kolb; Journal of Organic Chemistry; vol. 42; (1977); p. 359,360, View in Reaxys

Dichlorid: 35ClNQR-Sp.

Nesmeyanov et al.; Doklady Physical Chemistry; vol. 231; (1976); p. 1072, View in Reaxys

Charge-TransferKomplex mit I2

Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys

Charge-TransferKomplex mit Cl2

Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys

Charge-TransferKomplex mit Br2

Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys

H-Komplex m. tButylhydroperoxid: ν(S)(OH)

Bitman et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; (1974); p. 1361,1336,1337, View in Reaxys

ν-Komplex mit p-Nitro-m-trifluormethylphenol (NTP): IR (Tab.2)

Berthelot et al.; Journal of Molecular Structure; vol. 18; (1973); p. 435,441, View in Reaxys

TCNE- Komplex: vertikale PE-Jonis.energie und Charge-transferBandenmax. (Tab. 5)

Bock,H. et al.; Chemische Berichte; vol. 105; (1972); p. 3850 - 3864, View in Reaxys

mit O2: UV

Navmenko et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 2533,2562, View in Reaxys

Dichlorid: Rk. mit Verb. 1 -> Verb. 7

Masson,S.; Thuillier,A.; Bulletin de la Societe Chimique de France; nb. 12; (1969); p. 4368 4377, View in Reaxys

Komplex m. Hematoporphyrin: Abs.sp., K

Cann; Biochemistry; vol. 6; (1967); p. 3435,3436 - 3437, View in Reaxys

Verb. m. Tetracyanethylen (1:1): Charge-TransferKomplex; UV Max.

Voigt; Journal of the American Chemical Society; vol. 86; (1964); p. 3611,3614, View in Reaxys

Elektronen-Donator-Acceptor-Komplexbildung mit Tetracyanethylen: Charge-transfer-Sp.

Voigt; Reid; Journal of the American Chemical Society; vol. 86; (1964); p. 3930,3932, View in Reaxys

Benzaldehyd-2,4dinitrophenylhydrazon: F=235-237grad

Sharefkin; Forschirm; Analytical Chemistry; vol. 35; (1963); p. 1616,1618, View in Reaxys

Additionsverb. m.

Jod C6H5I*I2: Gleichgewichtskonstante bei 293, 313 u.333K; Temperaturabhaengigkeit der Gleichgewichtskonst.; Freie Enthalpie; Enthalpie; ΔS

Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 91, View in Reaxys

Komplex mit I2: Gleichgewicht-

Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 126, View in Reaxys

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skonst. u.Temperaturabhaengigkeit der Komplexbildung mit I2 von 293 bis 333K; Freie Bildungsenthalpie u. Bildungsentropie der Komplexbildung mit I2 bei 298K Komplexbildung m.

Essigsaeure, Buttersaeure, Phenol, Anisol, Me., A., Isopropanol

Bardamowa; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR; vol. 2; (1960); p. 71,72,73, View in Reaxys

compound with silver (+); Further Data see Handbook (Electrochemical behaviour)

Andrews; Keefer; Journal of the American Chemical Society; vol. 72; (1950); p. 3113, View in Reaxys

Melting Point (12) 1 of 12

Melting Point [°C]

-29

Leeke, Gary; Santos, Regina; Al-Duri, Bushra; Seville, Jonathan; Smith, Catherine; Holmes, Andrew B.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1370 - 1374, View in Reaxys 2 of 12

Melting Point [°C]

-31.55

Murthy, S. S. N.; Gangasharan; Nayak, S. K.; Journal of the Chemical Society, Faraday Transactions; vol. 89; nb. 3; (1993); p. 509 - 514, View in Reaxys 3 of 12

Melting Point [°C]

175 - 180

Banaerjee, Amalendu; Banerjee, Gopal Chandra; Bhattacharya, Sudin; Banerjee, Santa; Samaddar, Haraprasad; Journal of the Indian Chemical Society; vol. 58; (1981); p. 605 - 607, View in Reaxys 4 of 12

Melting Point [°C]

-31

Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys 5 of 12

Melting Point [°C]

-31.35

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys; Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys; Timmermans; Chem. Zentralbl.; vol. 85; nb. I; (1914); p. 618, View in Reaxys 6 of 12

Melting Point [°C]

-31.33

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys 7 of 12

Melting Point [°C]

-26

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 155, View in Reaxys 8 of 12

Melting Point [°C]

-29.1

Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys 9 of 12

Melting Point [°C]

-28.6

Menschutkin; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 419,422; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 380, View in Reaxys 10 of 12

Melting Point [°C]

-30.5

Holleman; de Bruyn; Recueil des Travaux Chimiques des Pays-Bas; vol. 20; (1901); p. 361, View in Reaxys 11 of 12

Melting Point [°C]

-28.5

v. Schneider; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 19; (1896); p. 157; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 22; (1897); p. 232, View in Reaxys 12 of 12

Melting Point [°C]

-29.8

Haase; Chemische Berichte; vol. 26; (1893); p. 1053, View in Reaxys

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Boiling Point (60) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

186 - 187

62

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Prishchenko, Andrey A.; Livantsov, Mikhail V.; Novikova, Olga P.; Livantsova, Ludmila I.; Petrosyan, Valery S.; Heteroatom Chemistry; vol. 23; nb. 4; (2012); p. 352 - 372, View in Reaxys

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438; nb. 2; (2011); p. 164 - 166, View in Reaxys

187 - 189

Firouzabadi; Iranpoor; Kazemi; Canadian Journal of Chemistry; vol. 87; nb. 12; (2009); p. 1675 - 1681, View in Reaxys

187

Butler, Richard N.; O'Shea, Paul D.; Shelly, Declan P.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1987); p. 1039 - 1042, View in Reaxys; Sathiyapriya; Karunakaran, R. Joel; Journal of Chemical Research; nb. 9; (2006); p. 575 - 576, View in Reaxys

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20

182 - 185

Zielinska, Agnieszka; Skulski, Lech; Molecules; vol. 10; nb. 10; (2005); p. 1307 - 1317, View in Reaxys Ogata; Aoki; Journal of the American Chemical Society; vol. 90; (1968); p. 6187, View in Reaxys; Yusubov; Zholobova; Filimonova; Chi, Ki-Whan; Russian Chemical Bulletin; vol. 53; nb. 8; (2004); p. 1735 - 1742, View in Reaxys

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Lulinski, Piotr; Skulski, Lech; Bulletin of the Chemical Society of Japan; vol. 72; nb. 1; (1999); p. 115 - 120, View in Reaxys; Lulinski, Piotr; Kryska, Anna; Sosnowski, Maciej; Skulski, Lech; Synthesis; nb. 3; (2004); p. 441 - 445, View in Reaxys

80 - 82

27

Lulinski, Piotr; Krassowska-Swiebocka, Barbara; Skulski, Lech; Molecules; vol. 9; nb. 7; (2004); p. 595 - 601, View in Reaxys

30 - 40

0.3

Makowiec, Slawomir; Rachon, Janusz; Phosphorus, Sulfur and Silicon and Related Elements; vol. 177; nb. 4; (2002); p. 941 - 955, View in Reaxys

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760

Chaikovski; Filimonov; Yagovkin; Ogorodnikov; Russian Chemical Bulletin; vol. 50; nb. 12; (2001); p. 2411 - 2415, View in Reaxys

73 - 77

34

Lulinski, Piotr; Skulski, Lech; Bulletin of the Chemical Society of Japan; vol. 73; nb. 4; (2000); p. 951 - 956, View in Reaxys

78 - 80

20

Kryska, Anna; Skulski, Lech; Journal of Chemical Research, Miniprint; nb. 10; (1999); p. 2501 2517, View in Reaxys

188.5

87 - 88

Bobyl et al.; Sov. Phys. J. (Engl. Transl.); vol. 6; (1965); p. 48,30, View in Reaxys; Gun'kin, I. F.; Russian Journal of General Chemistry; vol. 67; nb. 4; (1997); p. 654 - 655; Zhurnal Obshchei Khimii; vol. 67; nb. 4; (1997); p. 699 - 700, View in Reaxys 30

Lulinski, Piotr; Skulski, Lech; Bulletin of the Chemical Society of Japan; vol. 70; nb. 7; (1997); p. 1665 - 1669, View in Reaxys

188.4

Gun'kin, I. F.; Russian Journal of General Chemistry; vol. 65; nb. 3.2; (1995); p. 460; Zhurnal Obshchei Khimii; vol. 65; nb. 3; (1995); p. 518, View in Reaxys

186 - 188

Niemyjska, Maria; Skulski, Lech; Zdrojewska, Hanna; Bulletin of the Polish Academy of Sciences, Chemistry; vol. 38; nb. 1-12; (1990); p. 41 - 46, View in Reaxys

63 - 65

10

Bhattacharya et al.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 18; (1979); p. 231,232, View in Reaxys; Raizada, Meenu Singh; Nigam, H. L.; Journal of the Indian Chemical Society; vol. 63; (1986); p. 722 - 724, View in Reaxys

185 - 190

760

Aizpurua, J. M.; Juaristi, M.; Lecea, B.; Palomo, C.; Tetrahedron; vol. 41; nb. 14; (1985); p.

2903 - 2912, View in Reaxys

62

10

Saginova. L. G.; Bondarenko, O. B.; Shabarov, Yu. S.; Gazzaev, R. A.; Journal of Organic Chemistry USSR (English Translation); vol. 20; (1984); p. 1935 - 1939; Zhurnal Organicheskoi Khimii; vol. 20; nb. 10; (1984); p. 2124 - 2129, View in Reaxys

62

8

Livantsov, M. V.; Proskurnina, M. V.; Prishchenko, A. A.; Lutsenko, I. F.; J. Gen. Chem.

USSR (Engl. Transl.); vol. 54; nb. 11; (1984); p. 2504 - 2517,2237 - 2249, View in Reaxys

82

20

Citterio, Attilio; Arnold, Anna; Synthetic Communications; vol. 11; nb. 8; (1981); p. 639 - 642, View in Reaxys

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2018-06-17 20:23:57

69 - 70

15

Doleschall, Gabor; Toth, Gabor; Tetrahedron; vol. 36; (1980); p. 1649 - 1666, View in Reaxys

94

45

Kabalka; Ferrell; Synthetic Communications; vol. 9; (1979); p. 443,446, 447, View in Reaxys

188.6

Fridman; Mendeleev Chemistry Journal; vol. 22; (1977); p. 26; ; p. 110, View in Reaxys

184

Bhattacharya; Raj; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 15; (1977); p. 799, View in Reaxys

182

Bhattacharya; Raj; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 15; (1977); p. 799, View in Reaxys

73 - 74

10

Troyanker; Katsobashvili; Zhurnal Organicheskoi Khimii; vol. 12; (1976); p. 292,284, View in Reaxys

84 - 86

35

Rahman; Gilman; Journal of the Indian Chemical Society; vol. 51; (1974); p. 1018, View in Reaxys

77 - 78

20

Kameo; Manabe; Nippon Kagaku Kaishi; (1974); p. 195, View in Reaxys

183 - 184.5

Kikkawa et al.; Nippon Kagaku Kaishi; (1972); p. 625,626,627, View in Reaxys

184 - 186

Condon; Trivedi; Journal of Organic Chemistry; vol. 36; (1971); p. 1926,1929, View in Reaxys

54

3.8

Davison; Rakita; Journal of Organometallic Chemistry; vol. 23; (1970); p. 407,410,411,415,419, View in Reaxys

63

4

Snegur; Manulkin; J. Gen. Chem. USSR (Engl. Transl.); vol. 39; (1969); p. 1310,1281, View in Reaxys

76

Ptitsyna,O.A. et al.; Zhurnal Organicheskoi Khimii; vol. 5; nb. 3; (1969); p. 401 - 411,390 - 399, View in Reaxys

82 - 86

23

Cristol; Nachtigall; Journal of Organic Chemistry; vol. 32; (1967); p. 3727,3735, View in Reaxys

103.8 - 104

62

Aleksankin et al.; Zhurnal Organicheskoi Khimii; vol. 1; (1965); p. 1909,1947, View in Reaxys

185 - 186 73 - 74

Goto; Suzuki; Nippon Kagaku Zasshi; vol. 84; (1963); p. 167,168,173; Chem.Abstr.; vol. 59; nb.

15205; (1963), View in Reaxys 16

188

Guenther,H.; Chemische Berichte; vol. 96; (1963); p. 1801 - 1809, View in Reaxys Jackson; Sasse; Journal of the Chemical Society; (1962); p. 3746,3747, View in Reaxys

40 - 50

0.5

Forrest,J.; Journal of the Chemical Society; (1960); p. 574 - 580, View in Reaxys

25 - 45

0.5

Forrest,J.; Journal of the Chemical Society; (1960); p. 566 - 573, View in Reaxys

184 - 188

Minisci; Gazzetta Chimica Italiana; vol. 90; (1960); p. 1307,1315, View in Reaxys

188

760

Franzen; Chemische Berichte; vol. 87; (1954); p. 1148,1153, View in Reaxys

85

15

Haszeldine; Sharpe; Journal of the Chemical Society; (1952); p. 993,1000, View in Reaxys

190

763

Haszeldine; Sharpe; Journal of the Chemical Society; (1952); p. 993,1000, View in Reaxys

63 - 64

8

Lucas; Kennedy; Organic Syntheses; vol. Coll. Vol. II; (1943); p. 351, View in Reaxys

98

37

Hurdis; Smyth; Journal of the American Chemical Society; vol. 64; (1942); p. 2212,2214, View in Reaxys

188.4

768

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys

75

10

Kimura; Chemische Berichte; vol. 67; (1934); p. 394, View in Reaxys

79.6 - 79.8

20

Gross; Saylor; Gorman; Journal of the American Chemical Society; vol. 55; (1933); p. 650, View in Reaxys

188.45

760

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys; Young; Philos. Magazine; vol. <5> 50; p. 303, View in Reaxys

186

752

Sugden; Journal of the Chemical Society; vol. 125; (1924); p. 1173, View in Reaxys

189

Chattaway; Garton; Parkes; Journal of the Chemical Society; vol. 125; (1924); p. 1984, View in Reaxys

188.55

760

Timmermans; Chem. Zentralbl.; vol. 85; nb. I; (1914); p. 618, View in Reaxys

187.5

745.4

Rolla; Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti; vol. <5> 18 II; (1909); p. 371, View in Reaxys

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45/144

2018-06-17 20:23:57

69

15

Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys

187.7

760

Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1249, View in Reaxys

188.36

755.8

Feitler; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 4; (1889); p. 72, View in Reaxys

188.66

768.8

Feitler; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 4; (1889); p. 72, View in Reaxys

Refractive Index (54) Refractive Index Wavelength (ReTemperature (Refractive Index) [nm] fractive Index) [°C]

Comment (Refractive Index)

References

1.62

589

20

Voronkov; Vlasova; Belousova; Vlasov; Vakul'Skaya; Prozorova; Khutsishvili; Russian Journal of Organic Chemistry; vol. 49; nb. 1; (2013); p. 17 - 21; Zh. Org. Khim.; vol. 49; nb. 1; (2013); p. 27 31,5, View in Reaxys

1.621

589

20

Prishchenko, Andrey A.; Livantsov, Mikhail V.; Novikova, Olga P.; Livantsova, Ludmila I.; Petrosyan, Valery S.; Heteroatom Chemistry; vol. 23; nb. 4; (2012); p. 352 - 372, View in Reaxys

1.62

589

20

Vlasova; Belousova; Vlasov; Vakul'Skaya; Khutsishvili; Voronkov; Doklady Chemistry; vol. 438; nb.

2; (2011); p. 164 - 166, View in Reaxys

1.5464 - 1.6616

12703.3 - 24342.7

25

Keefe, C. Dale; Butler, Ellen; Gillis, Elizabeth; MacDonald, Jennifer L.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol.

67; nb. 1; (2007); p. 125 - 138, View in Reaxys

1.62

589

20

Mulholland; Zheng; Synthetic Communications; vol.

31; nb. 20; (2001); p. 3059 - 3068, View in Reaxys

1.6196

589

20

Kresge; Brown; Journal of Organic Chemistry; vol.

32; (1967); p. 756,757, View in Reaxys; Tsierkezos, Nikos G.; Palaiologou, Maria M.; Molinou, Ioanna E.; Journal of Chemical and Engineering Data; vol.

45; nb. 2; (2000); p. 272 - 275, View in Reaxys

1.619

589

20

Ptitsyna,O.A. et al.; Zhurnal Organicheskoi Khimii; vol. 5; nb. 3; (1969); p. 401 - 411,390 - 399, View in Reaxys; Gun'kin, I. F.; Russian Journal of General Chemistry; vol. 67; nb. 4; (1997); p. 654 655; Zhurnal Obshchei Khimii; vol. 67; nb. 4; (1997); p. 699 - 700, View in Reaxys

1.62

589

20

Bobyl et al.; Sov. Phys. J. (Engl. Transl.); vol. 6; (1965); p. 48,30, View in Reaxys; Gun'kin, I. F.; Russian Journal of General Chemistry; vol. 65; nb.

3.2; (1995); p. 460; Zhurnal Obshchei Khimii; vol. 65; nb. 3; (1995); p. 518, View in Reaxys

1.6141

589

20

Niemyjska, Maria; Skulski, Lech; Zdrojewska, Hanna; Bulletin of the Polish Academy of Sciences, Chemistry; vol. 38; nb. 1-12; (1990); p. 41 - 46, View in Reaxys

1.621

589

20

Fridman; Mendeleev Chemistry Journal; vol. 22; (1977); p. 26; ; p. 110, View in Reaxys; Livantsov, M. V.; Proskurnina, M. V.; Prishchenko, A. A.; Lutsenko, I. F.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 11; (1984); p. 2504 - 2517,2237 - 2249, View in Reaxys

1.6203

589

20

Saginova. L. G.; Bondarenko, O. B.; Shabarov, Yu. S.; Gazzaev, R. A.; Journal of Organic Chemistry USSR (English Translation); vol. 20; (1984); p. 1935 1939; Zhurnal Organicheskoi Khimii; vol. 20; nb. 10; (1984); p. 2124 - 2129, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

46/144

2018-06-17 20:23:57

1.5964 - 1.6335

6893.08 - 14934.5

20

Koeser, Heinz J. K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 2; (1984); p. 125 - 136, View in Reaxys

1.5865

589

25

Chawla, B.; Mehta, S. K.; Jasra, R. V.; Suri, S. K.; Canadian Journal of Chemistry; vol. 61; (1983); p.

2147 - 2150, View in Reaxys

1.6201

589

20

Lacourt et al.; Journal de Pharmacie de Belgique; vol. 8; (1953); p. 535,554; Microchimica Acta; (1953); p. 305,324, View in Reaxys; Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys

1.6194

589

20

Guenther,H.; Chemische Berichte; vol. 96; (1963); p.

1801 - 1809, View in Reaxys; Katritzky,A.R. et al.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); (1979); p. 433 - 435, View in Reaxys

1.6163

589

20

Rahman; Gilman; Journal of the Indian Chemical Society; vol. 51; (1974); p. 1018, View in Reaxys

1.62

589

1.643

589

20

Kiersznicki et al.; Roczniki Chemii; vol. 44; (1970); p. 1049, View in Reaxys

1.618

589

25

Kochi,J.K. et al.; Tetrahedron; vol. 24; (1968); p.

3503 - 3515, View in Reaxys

1.6197

589

20

Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys; Haberditzl; Koeppel; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 22; (1967); p. 691, View in Reaxys

1.619

589

21

Jackson; Sasse; Journal of the Chemical Society; (1962); p. 3746,3747, View in Reaxys

Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p.

673,678, View in Reaxys

1.6205

Luedde; Riechstoffe und Aromen; vol. 10; (1960); p.

193, View in Reaxys

1.6172

589

25

Lacourt et al.; Journal de Pharmacie de Belgique; vol. 8; (1953); p. 535,554; Microchimica Acta; (1953); p. 305,324, View in Reaxys

1.6228

589

15

Lacourt et al.; Journal de Pharmacie de Belgique; vol. 8; (1953); p. 535,554; Microchimica Acta; (1953); p. 305,324, View in Reaxys

1.6134

656.3

20

Vogel; Journal of the Chemical Society; (1948); p.

642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys; Karlsson,K.-J.; Diss. <Lund 1941> S. 73, 79, View in Reaxys

1.6204

589

20

Vogel; Journal of the Chemical Society; (1948); p.

642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

1.6384

486.1

20

Vogel; Journal of the Chemical Society; (1948); p.

642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

1.6535

434

20

Vogel; Journal of the Chemical Society; (1948); p.

642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

1.621

589

18

Miller; Bulletin des Societes Chimiques Belges; vol.

50; (1941); p. 51,55, View in Reaxys

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47/144

2018-06-17 20:23:57

1.61469

667.8

15

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.61559

656.3

15

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.62298

587.6

15

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.63735

492.1

15

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.64098

486.1

15

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.65221

447.1

15

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

1.6419

486.1

17.3

Voellmy; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 127; (1927); p. 345, View in Reaxys

1.6565

434

17.3

Voellmy; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 127; (1927); p. 345, View in Reaxys

1.6623 - 1.708

350 - 420

17.3

Voellmy; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 127; (1927); p. 345, View in Reaxys

1.6144

656.3

18.5

v. Auwers; Justus Liebigs Annalen der Chemie; vol.

422; (1921); p. 174, View in Reaxys

1.6214

589

18.5

v. Auwers; Justus Liebigs Annalen der Chemie; vol.

422; (1921); p. 174, View in Reaxys

1.6396

486.1

18.5

v. Auwers; Justus Liebigs Annalen der Chemie; vol.

422; (1921); p. 174, View in Reaxys

1.6552

434

18.5

v. Auwers; Justus Liebigs Annalen der Chemie; vol.

422; (1921); p. 174, View in Reaxys

1.6142

656.3

17.8

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.6213

589

17.8

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.6393

486.1

17.8

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys

1.57616

656.3

88

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.58265

589

88

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.61428

430.8

88

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.62003

656.3

8

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.62707

589

8

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.66126

430.8

8

Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys

1.6189

589

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

(:18-20 degreeC.

48/144

Seubert; Chemische Berichte; vol. 22; (1889); p.

2520, View in Reaxys

2018-06-17 20:23:57

1.6198

589

20

Karlsson,K.-J.; Diss. <Lund 1941> S. 73, 79, View in Reaxys

1.6385

486.1

20

Karlsson,K.-J.; Diss. <Lund 1941> S. 73, 79, View in Reaxys

Density (49) 1 of 49

Density [g·cm-3]

1.81

Location

supporting information

Xie, Xi; Ma, Shengming; Chemical Communications; vol. 49; nb. 50; (2013); p. 5693 - 5695, View in Reaxys 2 of 49

Density [g·cm-3]

1.82592

Measurement Temperature 20 [°C] Tsierkezos, Nikos G.; Palaiologou, Maria M.; Molinou, Ioanna E.; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 272 - 275, View in Reaxys 3 of 49

Density [g·cm-3]

1.8201

Measurement Temperature 25 [°C] Zainel, Hanaa A.; Al-Azzawi, Souad F.; Swellem, Hassan I.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 84; nb. 10; (1988); p. 3511 - 3516, View in Reaxys 4 of 49

Density [g·cm-3]

1.82361

Measurement Temperature 25 [°C] Chawla, B.; Mehta, S. K.; Jasra, R. V.; Suri, S. K.; Canadian Journal of Chemistry; vol. 61; (1983); p. 2147 - 2150, View in Reaxys 5 of 49

Density [g·cm-3]

1.7548 - 1.8316

Measurement Temperature 20 - 80 [°C] Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys 6 of 49

Density [g·cm-3]

1.8303

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Bruniquel et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 70; (1973); p. 1558, View in Reaxys 7 of 49

Density [g·cm-3]

1.801

Measurement Temperature 42 [°C] Curran; Curley; Analytical Chemistry; vol. 43; (1971); p. 118,119, View in Reaxys 8 of 49

Density [g·cm-3]

1.8319

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Kiersznicki et al.; Roczniki Chemii; vol. 44; (1970); p. 1049, View in Reaxys 9 of 49

Density [g·cm-3]

1.832

Measurement Temperature 20 [°C] Haberditzl; Koeppel; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 22; (1967); p. 691, View in Reaxys 10 of 49

Type (Density)

crystallographic

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

49/144

2018-06-17 20:23:57

Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys 11 of 49

Density [g·cm-3]

1.838

Luedde; Riechstoffe und Aromen; vol. 10; (1960); p. 193, View in Reaxys 12 of 49

Density [g·cm-3]

1.9041

Comment (Density)

von kristallinem Jodbenzol bei -35grad.

Kesemenli; Izv. Akad. Azerbajdzansk. S.S.R.; nb. 6; (1959); p. 53,54; Chem.Abstr.; (1961); p. 21714, View in Reaxys 13 of 49

Density [g·cm-3]

1.8971

Comment (Density)

von fluessigem Jodbenzol bei Temperaturen von -29grad.

Kesemenli; Izv. Akad. Azerbajdzansk. S.S.R.; nb. 6; (1959); p. 53,54; Chem.Abstr.; (1961); p. 21714, View in Reaxys 14 of 49

Density [g·cm-3]

1.8195

Comment (Density)

bis +25grad.

Kesemenli; Izv. Akad. Azerbajdzansk. S.S.R.; nb. 6; (1959); p. 53,54; Chem.Abstr.; (1961); p. 21714, View in Reaxys 15 of 49

Density [g·cm-3]

1.822

Measurement Temperature 20 [°C] Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p. 330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys 16 of 49

Density [g·cm-3]

1.7822 - 1.8431

Reference Temperature [°C]

4

Measurement Temperature 10 - 50 [°C] Lagemann; McMillan; Woolf; Journal of Chemical Physics; vol. 17; (1949); p. 370, View in Reaxys 17 of 49

Density [g·cm-3]

1.7331 - 1.8313

Reference Temperature [°C]

4

Measurement Temperature 20 - 87.5 [°C] Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys 18 of 49

Density [g·cm-3]

1.8307

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Audsley; Goss; Journal of the Chemical Society; (1942); p. 497,498, View in Reaxys; Karlsson,K.-J.; Diss.; <Lund 1941> S. 73, View in Reaxys 19 of 49

Density [g·cm-3]

1.86102

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 20 of 49

Density [g·cm-3]

1.83829

Reference Temperature [°C]

4

Measurement Temperature 15 [°C]

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

50/144

2018-06-17 20:23:57

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 21 of 49

Density [g·cm-3]

1.81548

Reference Temperature [°C]

4

Measurement Temperature 30 [°C] Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys 22 of 49

Density [g·cm-3]

1.8357

Reference Temperature [°C]

4

Measurement Temperature 17 [°C] Vorlaender; Fischer; Chemische Berichte; vol. 65; (1932); p. 1756,1759, View in Reaxys 23 of 49

Density [g·cm-3]

1.8324

Reference Temperature [°C]

4

Measurement Temperature 18.5 [°C] v. Auwers; Justus Liebigs Annalen der Chemie; vol. 422; (1921); p. 174, View in Reaxys 24 of 49

Density [g·cm-3]

1.631

Reference Temperature [°C]

4

Measurement Temperature 148.8 [°C] Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys 25 of 49

Density [g·cm-3]

1.854

Reference Temperature [°C]

4

Measurement Temperature 4.6 [°C] Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys 26 of 49

Density [g·cm-3]

1.709

Reference Temperature [°C]

4

Measurement Temperature 100 [°C] Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 155, View in Reaxys 27 of 49

Density [g·cm-3]

1.7852

Reference Temperature [°C]

4

Measurement Temperature 50 [°C] Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 155, View in Reaxys 28 of 49

Density [g·cm-3]

1.823

Reference Temperature [°C]

4

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Measurement Temperature 25 [°C] Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 155, View in Reaxys 29 of 49

Density [g·cm-3]

1.4172 - 1.8606

Reference Temperature [°C]

4

Measurement Temperature 0 - 270 [°C] Young; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 426, View in Reaxys 30 of 49

Density [g·cm-3]

1.8027

Reference Temperature [°C]

4

Measurement Temperature 38.5 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 31 of 49

Density [g·cm-3]

1.8138

Reference Temperature [°C]

4

Measurement Temperature 31.3 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 32 of 49

Density [g·cm-3]

1.82363

Reference Temperature [°C]

4

Measurement Temperature 24.8 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 33 of 49

Density [g·cm-3]

1.83257

Reference Temperature [°C]

4

Measurement Temperature 19.5 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys; Patterson; Mc Donald; Journal of the Chemical Society; vol. 93; (1908); p. 943, View in Reaxys 34 of 49

Density [g·cm-3]

1.8228

Reference Temperature [°C]

4

Measurement Temperature 25 [°C] Holleman; de Bruyn; Recueil des Travaux Chimiques des Pays-Bas; vol. 20; (1901); p. 361, View in Reaxys 35 of 49

Density [g·cm-3]

1.7832

Reference Temperature [°C]

100

Measurement Temperature 100 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys

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36 of 49

Density [g·cm-3]

1.792

Reference Temperature [°C]

75

Measurement Temperature 75 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 37 of 49

Density [g·cm-3]

1.8067

Reference Temperature [°C]

50

Measurement Temperature 50 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 38 of 49

Density [g·cm-3]

1.8283

Reference Temperature [°C]

25

Measurement Temperature 25 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 39 of 49

Density [g·cm-3]

1.8401

Reference Temperature [°C]

15

Measurement Temperature 15 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 40 of 49

Density [g·cm-3]

1.8551

Reference Temperature [°C]

4

Measurement Temperature 4 [°C] Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys 41 of 49

Density [g·cm-3]

1.72722

Reference Temperature [°C]

4

Measurement Temperature 88 [°C] Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys 42 of 49

Density [g·cm-3]

1.8482

Reference Temperature [°C]

4

Measurement Temperature 8 [°C] Perkin; Journal of the Chemical Society; vol. 61; (1892); p. 308, View in Reaxys 43 of 49

Density [g·cm-3]

1.83798

Reference Temperature [°C]

4

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Measurement Temperature 15.2 [°C] Young; Journal of the Chemical Society; vol. 55; (1889); p. 501; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 422, View in Reaxys 44 of 49

Density [g·cm-3]

1.86059

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Young; Journal of the Chemical Society; vol. 55; (1889); p. 501; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 422, View in Reaxys 45 of 49

Density [g·cm-3]

1.6486

Reference Temperature [°C]

4

Measurement Temperature 135.5 [°C] Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 563, View in Reaxys 46 of 49

Density [g·cm-3]

1.7374

Reference Temperature [°C]

4

Measurement Temperature 79.2 [°C] Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 563, View in Reaxys 47 of 49

Density [g·cm-3]

1.7732

Reference Temperature [°C]

4

Measurement Temperature 56.8 [°C] Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 563, View in Reaxys 48 of 49

Density [g·cm-3]

1.8403

Reference Temperature [°C]

4

Measurement Temperature 11 [°C] Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 563, View in Reaxys 49 of 49

Density [g·cm-3]

1.8578

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 563, View in Reaxys Adsorption (MCS) (12) 1 of 12

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

ethyl acetate

Partner (Adsorption (MCS))

3C12H6N2O4(2-)*2Y(3+)*3Pd(2+)*6Cl(1-)*11H2O

Huang, Jinping; Wang, Wei; Li, Hexing; ACS Catalysis; vol. 3; nb. 7; (2013); p. 1526 - 1536, View in Reaxys 2 of 12

Description (Adsorption (MCS))

Enthalpy of adsorption

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Partner (Adsorption (MCS))

MIL-47

Duerinck, Tim; Couck, Sarah; Baron, Gino V.; Denayer, Joeri F. M.; Vermoortele, Frederik; De Vos, Dirk E.; Langmuir; vol. 28; nb. 39; (2012); p. 13883 - 13891,9, View in Reaxys 3 of 12

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

15 - 35

Partner (Adsorption (MCS))

quartz sand

Arp, Hans Peter H.; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Toxicology and Chemistry; vol. 25; nb. 1; (2006); p. 45 - 51, View in Reaxys 4 of 12

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

single-wall carbon nanotube

Chattopadhyay, Jayanta; Sadana, Anil K.; Liang, Feng; Beach, Jonathan M.; Xiao, Yunxuan; Hauge, Robert H.; Billups; Organic Letters; vol. 7; nb. 19; (2005); p. 4067 - 4069, View in Reaxys 5 of 12

Description (Adsorption (MCS))

Chemisorption

Partner (Adsorption (MCS))

single-wall carbon nanotube

Chattopadhyay, Jayanta; Sadana, Anil K.; Liang, Feng; Beach, Jonathan M.; Xiao, Yunxuan; Hauge, Robert H.; Billups; Organic Letters; vol. 7; nb. 19; (2005); p. 4067 - 4069, View in Reaxys 6 of 12

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Solvent (Adsorption (MCS))

benzene

Temperature (Adsorption (MCS)) [°C]

4.9 - 19.9

Partner (Adsorption (MCS))

magnesium

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 274 - 276, View in Reaxys 7 of 12

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

benzene

Temperature (Adsorption (MCS)) [°C]

4.9 - 19.9

Partner (Adsorption (MCS))

magnesium

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 2; (1998); p. 274 - 276, View in Reaxys 8 of 12

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

-173.15 - 126.85

Partner (Adsorption (MCS))

Al2O3

Osaka, Naoki; Akita, Masato; Itoh, Koichi; Journal of Physical Chemistry B; vol. 102; nb. 35; (1998); p. 6817 - 6824, View in Reaxys 9 of 12

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

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Temperature (Adsorption (MCS)) [°C]

139.9 - 209.9

Partner (Adsorption (MCS))

graphitized thermal carbon black

Kalashnikova; Lopatkin; Russian Chemical Bulletin; vol. 46; nb. 12; (1997); p. 2060 - 2063, View in Reaxys 10 of 12

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

150

Partner (Adsorption (MCS))

BaSO4

Belyakova, L. D.; Larionov, O. G.; Strokina, L. M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 37; (1988); p. 1315 - 1320; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 7; (1988); p. 1491 - 1497, View in Reaxys 11 of 12

Description (Adsorption (MCS))

Enthalpy of adsorption

Kiselev et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 644; ; p. 1235, View in Reaxys; Kiselev et al.; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 705,706; ; p. 1272, View in Reaxys 12 of 12

Description (Adsorption (MCS))

Adsorption to title compound

Partner (Adsorption (MCS))

CO2

Just, G.; Z. Physik. Chem.; vol. 37; (1901); p. 342 - 367, View in Reaxys; vol. C: MVol.C1; 215, page 548 - 568 ; (from Gmelin), View in Reaxys Association (MCS) (33) 1 of 33

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

2,2,2-trifluoroethanol

Temperature (Association (MCS)) [°C]

20

Location

supporting information

Partner (Association (MCS))

(Na(I))42

Sarma, Bidyut Bikash; Avram, Liat; Neumann, Ronny; Chemistry - A European Journal; vol. 22; nb. 43; (2016); p. 15231 15236, View in Reaxys 2 of 33

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

D2O

Partner (Association (MCS))

4Ga(3+)*6[1,5-bis(1,2-di-O(1-)-C6H3-3-CONH)naphthalene]

Hastings, Courtney J.; Pluth, Michael D.; Biros, Shannon M.; Bergman, Robert G.; Raymond, Kenneth N.; Tetrahedron; vol. 64; nb. 36; (2008); p. 8362 - 8367, View in Reaxys 3 of 33

Description (Association (MCS))

IR spectrum of the complex

Partner (Association (MCS))

single-wall carbon nanotube

Chattopadhyay, Jayanta; Sadana, Anil K.; Liang, Feng; Beach, Jonathan M.; Xiao, Yunxuan; Hauge, Robert H.; Billups; Organic Letters; vol. 7; nb. 19; (2005); p. 4067 - 4069, View in Reaxys 4 of 33

Description (Association (MCS))

Further physical properties of the complex

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Partner (Association (MCS))

L99A

Graves, Alan P.; Brenk, Ruth; Shoichet, Brian K.; Journal of Medicinal Chemistry; vol. 48; nb. 11; (2005); p. 3714 - 3728, View in Reaxys 5 of 33

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

acetonitrile; hexamethylphosphoric acid triamide

Partner (Association (MCS))

SmCl3

Budnikova; Yakhvarov; Kargin; Russian Journal of General Chemistry; vol. 68; nb. 4; (1998); p. 566 - 569, View in Reaxys 6 of 33

Description (Association (MCS))

Further physical properties of the complex

Temperature (Association (MCS)) [°C]

-163.15

Partner (Association (MCS))

Al2O3

Osaka, Naoki; Akita, Masato; Itoh, Koichi; Journal of Physical Chemistry B; vol. 102; nb. 35; (1998); p. 6817 - 6824, View in Reaxys 7 of 33

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

acetonitrile

Partner (Association (MCS))

2,4,6-triphenylpyrylium tetrafluoroborate

Jayanthi; Ramamurthy; Journal of Physical Chemistry A; vol. 101; nb. 11; (1997); p. 2016 - 2022, View in Reaxys 8 of 33

Description (Association (MCS))

UV/VIS spectrum of the complex

Partner (Association (MCS))

ethenetetracarbonitrile

Frey, John E.; Aiello, Theresa; Fu, Shi-Lin; Hutson, Heather; Journal of Organic Chemistry; vol. 61; nb. 1; (1996); p. 295 300, View in Reaxys 9 of 33

Description (Association (MCS))

Stability constant of the complex with ...

Partner (Association (MCS))

ethenetetracarbonitrile

Frey, John E.; Aiello, Theresa; Fu, Shi-Lin; Hutson, Heather; Journal of Organic Chemistry; vol. 61; nb. 1; (1996); p. 295 300, View in Reaxys 10 of 33

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

ethenetetracarbonitrile

Frey, John E.; Aiello, Theresa; Fu, Shi-Lin; Hutson, Heather; Journal of Organic Chemistry; vol. 61; nb. 1; (1996); p. 295 300, View in Reaxys 11 of 33

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

C144H136O28

Byun, Young-Seok; Vadhat, Omid; Blanda, Michael T.; Knobler, Carolyn B.; Cram, Donald J.; Journal of the Chemical Society, Chemical Communications; nb. 17; (1995); p. 1825 - 1828, View in Reaxys 12 of 33

Description (Association (MCS))

NMR spectrum of the complex

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Solvent (Association (MCS))

CDCl3

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

C144H136O24

Robbins, Timothy A.; Knobler, Carolyn B.; Bellew, Donald R.; Cram, Donald J.; Journal of the American Chemical Society; vol. 116; nb. 1; (1994); p. 111 - 122, View in Reaxys 13 of 33

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ν-cyclodextrin

Sanemasa, Isao; Wu, Yue; Koide, Yuuki; Shigenaga, Masako; Ishibashi, Kazunari; Deguchi, Toshio; Bulletin of the Chemical Society of Japan; vol. 66; nb. 5; (1993); p. 1424 - 1429, View in Reaxys 14 of 33

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

alpha cyclodextrin

Sanemasa, Isao; Wu, Yue; Koide, Yuuki; Shigenaga, Masako; Ishibashi, Kazunari; Deguchi, Toshio; Bulletin of the Chemical Society of Japan; vol. 66; nb. 5; (1993); p. 1424 - 1429, View in Reaxys 15 of 33

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

cyclomaltooctaose

Sanemasa, Isao; Wu, Yue; Koide, Yuuki; Shigenaga, Masako; Ishibashi, Kazunari; Deguchi, Toshio; Bulletin of the Chemical Society of Japan; vol. 66; nb. 5; (1993); p. 1424 - 1429, View in Reaxys 16 of 33

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

acetonitrile

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

NOBF4

Bockman; Karpinski; Sankararaman; Kochi; Journal of the American Chemical Society; vol. 114; nb. 6; (1992); p. 1970 1985, View in Reaxys 17 of 33

Description (Association (MCS))

NMR spectrum of the complex

Solvent (Association (MCS))

tetrahydrofuran

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Temperature (Association (MCS)) [°C]

-105

Partner (Association (MCS))

phenyllithium

Okazaki, Renji; Tokitoh, Norihiro; Ishii, Akihiko; Ishii, Naoko; Matsuhashi, Yasusuke; et al.; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 67; nb. 1-4; (1992); p. 49 - 66, View in Reaxys 18 of 33

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

Hexadecane

Abraham, Michael H.; Whiting, Gary S.; Fuchs, Richard; Chambers, Eric J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 2; (1990); p. 291 - 300, View in Reaxys 19 of 33

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

alpha cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 20 of 33

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

alpha cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 21 of 33

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ν-cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 22 of 33

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

ν-cyclodextrin

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys

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23 of 33

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

cyclomaltooctaose

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 24 of 33

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

cyclomaltooctaose

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 25 of 33

Description (Association (MCS))

NMR spectrum of the complex

Temperature (Association (MCS)) [°C]

32

Partner (Association (MCS))

1-methyl-pyrrolidin-2-one

Zainel, Hanaa A.; Al-Azzawi, Souad F.; Swellem, Hassan I.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 84; nb. 10; (1988); p. 3511 - 3516, View in Reaxys 26 of 33

Description (Association (MCS))

Enthalpy of association

Partner (Association (MCS))

phenylnitrenium ion

Meot-Ner (Mautner), Michael; El-Shall, M. Samy; Journal of the American Chemical Society; vol. 108; nb. 15; (1986); p.

4386 - 4390, View in Reaxys 27 of 33

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

phenylnitrenium ion

Meot-Ner (Mautner), Michael; El-Shall, M. Samy; Journal of the American Chemical Society; vol. 108; nb. 15; (1986); p.

4386 - 4390, View in Reaxys 28 of 33

Description (Association (MCS))

IR spectrum of the complex

Temperature (Association (MCS)) [°C]

35 - 55

Partner (Association (MCS))

N-(4-ethoxybenzylidene)-4-butylaniline

Chingduang, P.; Bualek, S.; Phaovibul, O.; Schrader, B.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 132; (1986); p. 131 - 142, View in Reaxys 29 of 33

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

2,4,6-trinitrochlorobenzene

Basu, Rama; Journal of the Indian Chemical Society; vol. 63; (1986); p. 105 - 107, View in Reaxys

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30 of 33

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

CCl4

Partner (Association (MCS))

ethenetetracarbonitrile

Gol'dshtein, I. P.; Fedotov, A. N.; Starostina, T. A.; Rybakova, L. F.; Gur'yanova, E. N.; J. Gen. Chem. USSR (Engl.

Transl.); vol. 54; nb. 6; (1984); p. 1363 - 1374,1218 - 1227, View in Reaxys 31 of 33

Description (Association (MCS))

UV/VIS spectrum of the complex

Partner (Association (MCS))

benzene

Scaiano; Stewart; Journal of the American Chemical Society; vol. 105; nb. 11; (1983); p. 3609 - 3614, View in Reaxys 32 of 33

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

cyclohexane

Temperature (Association (MCS)) [°C]

24.9

Partner (Association (MCS))

iodine

Shedbalkar, V. P.; Bhat, S. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical and Analytical; vol. 22; nb. 12; (1983); p. 1062 - 1064, View in Reaxys 33 of 33

Description (Association (MCS))

Association with compound

Voigt; Journal of Physical Chemistry; vol. 72; (1968); p. 3300, View in Reaxys; Foster et al.; Journal of Pharmaceutical Sciences; vol. 67; (1978); p. 1310,1312, View in Reaxys; Olszer; Siekierski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 14; (1966); p. 325, View in Reaxys Azeotropes (MCS) (55) 1 of 55

Temperature (Azeotropes (MCS)) [°C]

188.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

p-cresol

Lecat; Ann. Soc. scient. Bruxelles; vol. 49; (1929); p. 111, View in Reaxys 2 of 55

Temperature (Azeotropes (MCS)) [°C]

154.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys; Lecat; Ann. Soc. scient. Bruxelles; vol. 49; (1929); p. 111, View in Reaxys 3 of 55

Temperature (Azeotropes (MCS)) [°C]

182

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

aniline

Lecat,M.; Recueil des Travaux Chimiques des Pays-Bas; vol. 47; (1928); p. 15,16; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 154, View in Reaxys 4 of 55

Temperature (Azeotropes (MCS)) [°C]

161.6

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61/144

2018-06-17 20:23:57

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyric acid

Lecat; Ann. Soc. scient. Bruxelles; vol. 48 I; (1928); p. 119, View in Reaxys 5 of 55

Temperature (Azeotropes (MCS)) [°C]

181

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diethyl oxalate

Lecat; Ann. Soc. scient. Bruxelles; vol. 48 I; (1928); p. 119, View in Reaxys 6 of 55

Temperature (Azeotropes (MCS)) [°C]

178

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

dimethyl malonate

Lecat; Ann. Soc. scient. Bruxelles; vol. 48 I; (1928); p. 119, View in Reaxys 7 of 55

Temperature (Azeotropes (MCS)) [°C]

174

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isovaleric acid

Lecat; Ann. Soc. scient. Bruxelles; vol. 48 I; (1928); p. 119, View in Reaxys 8 of 55

Temperature (Azeotropes (MCS)) [°C]

187.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

octyl alcohol

Lecat; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 68, View in Reaxys 9 of 55

Temperature (Azeotropes (MCS)) [°C]

171.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethylene glycol

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p.

112,151,155, View in Reaxys 10 of 55

Temperature (Azeotropes (MCS)) [°C]

178.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

#sec!-octyl alcohol

Lecat; Ann. Soc. scient. Bruxelles; vol. 47 I; (1927); p. 68, View in Reaxys 11 of 55

Temperature (Azeotropes (MCS)) [°C]

173

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

glycerol-ν.ν'-dichlorohydrin

Lecat; Recueil des Travaux Chimiques des Pays-Bas; vol. 46; (1927); p. 243; Ann.Soc.scient.Bruxelles; vol. 47 I; (1927); p.

112,151,155, View in Reaxys

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62/144

2018-06-17 20:23:57

12 of 55

Temperature (Azeotropes (MCS)) [°C]

181.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

aniline

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 13 of 55

Temperature (Azeotropes (MCS)) [°C]

177.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 14 of 55

Temperature (Azeotropes (MCS)) [°C]

180.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetamide

Lecat; Ann. Soc. scient. Bruxelles; vol. 47; p. I, 151, 154, View in Reaxys 15 of 55

Temperature (Azeotropes (MCS)) [°C]

180

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetamide

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 16 of 55

Temperature (Azeotropes (MCS)) [°C]

188.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

o-toluidine

Lecat; Ann. Soc. scient. Bruxelles; vol. 47; p. I, 151, 154, View in Reaxys 17 of 55

Temperature (Azeotropes (MCS)) [°C]

185

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

#o!-cresol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 18 of 55

Temperature (Azeotropes (MCS)) [°C]

187.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

#p!-cresol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 19 of 55

Temperature (Azeotropes (MCS)) [°C]

183.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propylamine

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

63/144

2018-06-17 20:23:57

20 of 55

Temperature (Azeotropes (MCS)) [°C]

186.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

hexanoic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 21 of 55

Temperature (Azeotropes (MCS)) [°C]

187.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

octanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 22 of 55

Temperature (Azeotropes (MCS)) [°C]

183.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propionamide

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 23 of 55

Temperature (Azeotropes (MCS)) [°C]

186.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

dimethylaniline

Lecat; Ann. Soc. scient. Bruxelles; vol. 47; p. I, 151, 154, View in Reaxys 24 of 55

Temperature (Azeotropes (MCS)) [°C]

170.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethylene glycol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 25 of 55

Temperature (Azeotropes (MCS)) [°C]

180.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

valeric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 26 of 55

Temperature (Azeotropes (MCS)) [°C]

179.7

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<=179.7gradC; Gewprozent >26.

Azeotropes

octanol-(2)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 27 of 55

Temperature (Azeotropes (MCS)) [°C]

187

Pressure (Azeotropes (MCS)) [Torr]

760

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64/144

2018-06-17 20:23:57

Comment (Azeotropes (MCS))

Verbindung (1)::T<187gradC;.

Azeotropes

benzonitrile

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 28 of 55

Temperature (Azeotropes (MCS)) [°C]

175.3

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

chloroacetic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 29 of 55

Temperature (Azeotropes (MCS)) [°C]

163.5

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T=163.5gradC(?); Gewprozent =28.

Azeotropes

butyric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 30 of 55

Temperature (Azeotropes (MCS)) [°C]

173.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isovaleric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 31 of 55

Temperature (Azeotropes (MCS)) [°C]

187.7

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<187.7gradC; Gewprozent >88.

Azeotropes

benzyl alcohol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 32 of 55

Temperature (Azeotropes (MCS)) [°C]

183.5

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<183.5gradC; Gewprozent >49.

Azeotropes

dimethyl sulfate

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 33 of 55

Temperature (Azeotropes (MCS)) [°C]

176

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<176gradC; Gewprozent >22.

Azeotropes

2-chloro-phenol

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

65/144

2018-06-17 20:23:57

34 of 55

Temperature (Azeotropes (MCS)) [°C]

184.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

trichloroacetic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 35 of 55

Temperature (Azeotropes (MCS)) [°C]

184.3

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<184.3gradC; Gewprozent =88.

Azeotropes

bromoacetic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 36 of 55

Temperature (Azeotropes (MCS)) [°C]

161

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2-amino-ethanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 37 of 55

Temperature (Azeotropes (MCS)) [°C]

185.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

4-methyl-valeric acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 38 of 55

Temperature (Azeotropes (MCS)) [°C]

180.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

oxalic acid diethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 39 of 55

Temperature (Azeotropes (MCS)) [°C]

173

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

1.3-dichloro-propanol-(2)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 40 of 55

Temperature (Azeotropes (MCS)) [°C]

177.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2.3-dichloro-propanol-(1)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 41 of 55

Temperature (Azeotropes (MCS)) [°C]

183.5

Pressure (Azeotropes (MCS)) [Torr]

760

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66/144

2018-06-17 20:23:57

Comment (Azeotropes (MCS))

Verbindung (1)::T<183.5gradC; Gewprozent >42.

Azeotropes

1.2-diacetoxy-ethane

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 42 of 55

Temperature (Azeotropes (MCS)) [°C]

184.8

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<184.8gradC.

Azeotropes

2-bromo-propionic acid

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 43 of 55

Temperature (Azeotropes (MCS)) [°C]

186.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

fumaric acid dimethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 44 of 55

Temperature (Azeotropes (MCS)) [°C]

180.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

lactic acid isobutyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 45 of 55

Temperature (Azeotropes (MCS)) [°C]

174

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

carbamic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 46 of 55

Temperature (Azeotropes (MCS)) [°C]

178

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetoacetic acid ethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 47 of 55

Temperature (Azeotropes (MCS)) [°C]

170.8

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<170.8gradC.

Azeotropes

1-butyloxy-ethanol-(2)

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 48 of 55

Temperature (Azeotropes (MCS)) [°C]

188.3

Pressure (Azeotropes (MCS)) [Torr]

760

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67/144

2018-06-17 20:23:57

Comment (Azeotropes (MCS))

Verbindung (1)::T<183.3gradC.

Azeotropes

acetic acid phenyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 49 of 55

Temperature (Azeotropes (MCS)) [°C]

178.2

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<178.2gradC; Gewprozent >31.

Azeotropes

malonic acid dimethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 50 of 55

Temperature (Azeotropes (MCS)) [°C]

187.2

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<87.25gradC; Gewprozent >77.

Azeotropes

malonic acid diethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 51 of 55

Temperature (Azeotropes (MCS)) [°C]

181.2

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<181.2gradC; Gewprozent >12.

Azeotropes

chloroacetic acid butyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 52 of 55

Temperature (Azeotropes (MCS)) [°C]

185.3

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<185.3gradC; Gewprozent >58.

Azeotropes

carbonic acid diisobutyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 53 of 55

Temperature (Azeotropes (MCS)) [°C]

185.8

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<185.8gradC; Gewprozent >70.

Azeotropes

succinic acid dimethyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 54 of 55

Temperature (Azeotropes (MCS)) [°C]

184

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetic acid-<2-hydroxy-ethyl ester>

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68/144

2018-06-17 20:23:57

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys 55 of 55

Temperature (Azeotropes (MCS)) [°C]

188.3

Pressure (Azeotropes (MCS)) [Torr]

760

Comment (Azeotropes (MCS))

Verbindung (1)::T<188.3gradC; Gewprozent >87.

Azeotropes

isovaleric acid isopentyl ester

Lecat,M.; Tables azeotropiques, 2. Aufl. <Bruessel 1949>, View in Reaxys Boundary Surface Phenomena (MCS) (6) 1 of 6

Description (Boundary Surface Phenomena (MCS))

Further surface properties

Solvent (Boundary Surface neat (no solvent) Phenomena (MCS)) Partner (Boundary Surface Au(111) Phenomena (MCS)) Koel; Barney Ellison; Syomin; Kim; Journal of Physical Chemistry B; vol. 105; nb. 35; (2001); p. 8387 - 8394, View in Reaxys 2 of 6

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Wolf; Neumann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 219; (1962); p. 60,77,78, View in Reaxys 3 of 6

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser bei Temperaturen von 20grad bis 70grad.

Jasper; Wood; Journal of Physical Chemistry; vol. 60; (1956); p. 1625, View in Reaxys 4 of 6

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser bei Temperaturen von 20grad bis 80grad.

Jasper; Wood; Journal of Physical Chemistry; vol. 59; (1955); p. 541, View in Reaxys 5 of 6

Description (Boundary Surface Phenomena (MCS))

Contact angle with compound

Partner (Boundary Surface iodobenzene; air Phenomena (MCS)) Bartell; Merrill; Journal of Physical Chemistry; vol. 36; (1932); p. 1178,1184, View in Reaxys; Bartell; Whitney; Journal of Physical Chemistry; vol. 36; (1932); p. 3115,3122, View in Reaxys 6 of 6

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser.

Harkins; Brown; Davies; Journal of the American Chemical Society; vol. 39; (1917); p. 357, View in Reaxys; Harkins; Feldman; Journal of the American Chemical Society; vol. 44; (1922); p. 2671, View in Reaxys; Hardy; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 88; (1913); p. 311; Chem. Zentralbl.; vol.

84; nb. II; (1913); p. 403, View in Reaxys Chromatographic Data (6) Chromatographic Location data

References

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

69/144

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GC (Gas chromatography)

supporting informa- Xu, Mei; Zhang, Xiao-Hong; Shao, Yin-Lin; Han, Jiang-Sheng; Zhong, Ping; Advanced Syntion thesis and Catalysis; vol. 354; nb. 14-15; (2012); p. 2665 - 2670, View in Reaxys; Dennig, Alexander; Luelsdorf, Nina; Liu, Haifeng; Schwaneberg, Ulrich; Angewandte Chemie - International Edition; vol. 52; nb. 32; (2013); p. 8459 - 8462; Angew. Chem.; vol. 125; nb. 32; (2013); p. 8617 - 8620,4, View in Reaxys; Ho, Phyllis E.; Tao, Jason; Murphy, Graham K.; European Journal of Organic Chemistry; nb. 29; (2013); p. 6540 - 6544, View in Reaxys; Napoly, Francois; Jean-Gerard, Ludivine; Goux-Henry, Catherine; Draye, Micheline; Andrioletti, Bruno; European Journal of Organic Chemistry; vol. 2014; nb. 4; (2014); p. 781 - 787, View in Reaxys; Reddy, N. Veera; Prasad, K. Rajendra; Reddy, P. Sudhir; Lakshmi Kantam; Reddy, K. Rajender; Organic and Biomolecular Chemistry; vol. 12; nb. 14; (2014); p. 2172 - 2175, View in Reaxys; Zhu, Hui; Zhang, Shusheng; Wang, Haoyang; Xu, Bin; Guo, Yinlong; Chinese Journal of Chemistry; vol. 33; nb. 12; (2015); p. 1365 - 1370, View in Reaxys; Losch; Kolb; Astafan; Daou; Pinard; Pale; Louis; Green Chemistry; vol. 18; nb. 17; (2016); p. 4714 - 4724, View in Reaxys; Mi, Chun; Li, Lu; Meng, Xiang-Guang; Yang, Ren-Qiang; Liao, Xiao-Hong; Tetrahedron; vol. 72; nb. 42; (2016); p. 6705 - 6710, View in Reaxys; Ni, Shengyang; Zhang, Wenzhong; Mei, Haibo; Han, Jianlin; Pan, Yi; Organic Letters; vol. 19; nb. 10; (2017); p. 2536 - 2539, View in Reaxys; Felipe-Blanco, Diego; Alonso, Francisco; Gonzalez-Gomez, Jose C.; Advanced Synthesis and Catalysis; vol. 359; nb. 16; (2017); p. 2857 - 2863, View in Reaxys; Almasalma, Ahmad A.; Mejía, Esteban; European Journal of Organic Chemistry; vol. 2018; nb. 2; (2018); p. 188 - 195, View in Reaxys; Zhang, Xiaoyan; Sun, Zaicheng; Wang, Bin; Tang, Yu; Nguyen, Luan; Li, Yuting; Tao, Franklin Feng; Journal of the American Chemical Society; vol.

140; nb. 3; (2018); p. 954 - 962, View in Reaxys

HPLC (High performance liquid chromatography)

supporting informa- Filice, Marco; Romero, Oscar; Aires, Antonio; Guisan, Jose M.; Rumbero, Angel; Palomo, tion Jose M.; Advanced Synthesis and Catalysis; vol. 357; nb. 12; (2015); p. 2687 - 2696, View in Reaxys; Arun; Reddy, P. O. Venkataramana; Pilania, Meenakshi; Kumar, Dalip; European Journal of Organic Chemistry; vol. 2016; nb. 12; (2016); p. 2096 - 2100, View in Reaxys; Shin, Hyeon Ho; Kang, Eunmi; Park, Haeli; Han, Taejun; Lee, Chul-Ho; Lim, Dong-Kwon; Journal of Materials Chemistry A; vol. 5; nb. 47; (2017); p. 24965 - 24971, View in Reaxys

HPLC (High performance liquid chromatography)

Liu, Xi-Hai; Leng, Jing; Jia, Su-Jiao; Hao, Jian-Hong; Zhang, Fanglin; Qin, Hua-Li; Zhang, Cheng-Pan; Journal of Fluorine Chemistry; vol. 189; (2016); p. 59 - 67, View in Reaxys; Rauber, Daniel; Philippi, Frederik; Hempelmann, Rolf; Journal of Fluorine Chemistry; vol. 200; (2017); p. 115 - 122, View in Reaxys

TLC (Thin layer chromatography)

Krishna, Jonnada; Krishna Reddy, Alavala Gopi; Satyanarayana, Gedu; Advanced Synthesis and Catalysis; vol. 357; nb. 16-17; (2015); p. 3597 - 3610, View in Reaxys; Suchand, Basuli; Satyanarayana, Gedu; Journal of Organic Chemistry; vol. 81; nb. 15; (2016); p. 6409 - 6423, View in Reaxys

TLC (Thin layer chromatography)

supporting informa- Krishna, Jonnada; Reddy, Alavala Gopi Krishna; Satyanarayana, Gedu; Synthetic Communition cations; vol. 44; nb. 14; (2014); p. 2103 - 2111, View in Reaxys; Ravi Kumar, Devarapalli; Satyanarayana, Gedu; Organic Letters; vol. 17; nb. 23; (2015); p. 5894 - 5897, View in Reaxys

GC (Gas chromatography)

Collins, Karl D.; Glorius, Frank; Tetrahedron; vol. 69; nb. 36; (2013); p. 7817 - 7825, View in Reaxys

Compressibility (1) Description (Com- Comment (Compressibility) pressibility)

References

Adiabatic compres- im Temperaturbersibility eich von 10grad bis 50grad.

Lagemann; McMillan; Woolf; Journal of Chemical Physics; vol. 17; (1949); p. 370, View in Reaxys; Lagemann; Evans; McMillan; Journal of the American Chemical Society; vol.

70; (1948); p. 2997, View in Reaxys

Conformation (2) Object of Investiga- References tion Conformation

Fimmel, Benjamin; Son, Minjung; Sung, Young Mo; Grüne, Matthias; Engels, Bernd; Kim, Dongho; Würthner, Frank; Chemistry - A European Journal; vol. 21; nb. 2; (2015); p. 615 - 630, View in Reaxys

Conformation

Russel et al.; Journal of the Chemical Society, Chemical Communications; (1977); p. 427, View in Reaxys

Critical Temperature (1) Critical TemperaReferences ture [°C] 448

Young; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 626; Scientific Proceedings of the Royal Dublin Society; vol. 12; (1909); p. 432, View in Reaxys

Critical Volume (2) Comment (Critical References Volume)

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Joliet; Berthon; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 260; (1965); p. 2805, View in Reaxys; Bhagvanth Rao et al.; Journal of the Indian Institute of Science; vol. 53; (1971); p. 99,103, View in Reaxys 1.720 cm3/g.

Young; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 626; Scientific Proceedings of the Royal Dublin Society; vol. 12; (1909); p. 432, View in Reaxys

Crystal Phase (3) Description (Crystal Phase)

Comment (Crystal Phase)

Rate of transition Crystal structure determination

Cheng, P.Y.; Zhong, D.; Zewail, Ahmed H.; Chemical Physics Letters; vol. 237; nb. 5,6; (1995); p. 399 - 405, View in Reaxys .

Solid state structure properties

Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys

Crystal Property Description (6) Colour & Other Location Properties colourless

References

References

supporting informa- Niu, Liting; Zhang, Hao; Yang, Haijun; Fu, Hua; Synlett; vol. 25; nb. 7; (2014); p. 995 - 1000; tion Art.No: 691, View in Reaxys; Liu, Wenbo; Yang, Xiaobo; Gao, Yang; Li, Chao-Jun; Journal of the American Chemical Society; vol. 139; nb. 25; (2017); p. 8621 - 8627, View in Reaxys

colourless

Verhasselt, Sigrid; Roman, Bart I.; De Wever, Olivier; Van Hecke, Kristof; Van Deun, Rik; Bracke, Marc E.; Stevens, Christian V.; Organic and Biomolecular Chemistry; vol. 15; nb. 9; (2017); p. 2104 - 2118, View in Reaxys

white

Bergström, Maria; Suresh, Ganji; Naidu, Veluru Ramesh; Unelius, C. Rikard; European Journal of Organic Chemistry; vol. 2017; nb. 22; (2017); p. 3234 - 3239, View in Reaxys

yellow

Li, Pengfei; Cheng, Guolin; Zhang, Hong; Xu, Xianxiang; Gao, Jingyuan; Cui, Xiuling; Journal of Organic Chemistry; vol. 79; nb. 17; (2014); p. 8156 - 8162, View in Reaxys

colourless

Yang, Haijun; Li, Yong; Jiang, Min; Wang, Junmei; Fu, Hua; Chemistry - A European Journal; vol. 17; nb. 20; (2011); p. 5652 - 5660, View in Reaxys

white

Page/Page column 36

Patent; Chen, Li; Feng, Lichun; Huang, Mengwei; Liu, Yongfu; Wu, Guolong; Wu, Jim Zhen; Zhou, Mingwei; US2011/257151; (2011); (A1) English, View in Reaxys

Decomposition (1) 1 of 1

Momigny; Bulletin des Societes Chimiques Belges; vol. 70; (1961); p. 291, View in Reaxys

Dielectric Constant (7) Dielectric Constant Frequency (Dielectric Constant) [Hz]

Temperature (Dielectric Constant) [°C]

References

0.00844 - 1.71

2.18397E+13 9.04137E+13

25

Keefe, C. Dale; Butler, Ellen; Gillis, Elizabeth; MacDonald, Jennifer L.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 1; (2007); p. 125 - 138, View in Reaxys

4.75

2E+06

20

Laurence, Christian; Nicolet, Pierre; Dalati, M. Tawfik; Abboud, JoseLuis M.; Notario, Rafael; Journal of Physical Chemistry; vol. 98; nb. 23; (1994); p. 5807 - 5816, View in Reaxys Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p.

1389,1394, View in Reaxys; Hartmann; Schmidt; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 62; (1968); p. 312, View in Reaxys; Hartmann; Schmidt; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 875, View in Reaxys; Deich; J. Gen. Chem. USSR (Engl.

Transl.); vol. 48; (1978); p. 975,891, View in Reaxys; Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys; Luedde; Riechstoffe und Aromen; vol.

10; (1960); p. 193, View in Reaxys; Imanow et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 238; (1968); p. 133, View in Reaxys; Okabayashi; Bulletin of the Chemical Society of Japan; vol. 35; (1962); p. 163, View in Reaxys; Imanow; Sul'fugarzade; Russian Journal of Physical Chemistry; vol. 38; (1964); p. 1314; Zhurnal Fizicheskoi Khimii; vol. 38; (1964); p. 2437, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys

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4.6

7.5188E+09

21

Poley; Appl. scient. Res.; vol. <B> 4; (1955); p. 337,368, View in Reaxys

3.74065E+10

21

Poley; Appl. scient. Res.; vol. <B> 4; (1955); p. 337,368, View in Reaxys

7.05882E+06

20

Ebert; Zeitschrift fuer Analytische Chemie; vol. 140; (1953); p. 161,163, View in Reaxys

5E+08

20.4

Dobrosserdow; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 125; Chem. Zentralbl.; vol. 82; nb. I; (1911); p. 955, View in Reaxys

Dissociation Energy (3) Dissociation Ener- Bond Type gy [Jmol-1]

References

281353

Galli, Carlo; Pau, Tullia; Tetrahedron; vol. 54; nb. 12; (1998); p. 2893 - 2904, View in Reaxys

C-I

Kominar et al.; Canadian Journal of Chemistry; vol. 56; (1978); p. 1589, View in Reaxys C6H5-I Dynamic Viscosity (8) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

Szwarc; Williams; Journal of Chemical Physics; vol. 20; (1952); p. 1171, View in Reaxys References

0.01736

20

Tsierkezos, Nikos G.; Palaiologou, Maria M.; Molinou, Ioanna E.; Journal of Chemical and Engineering Data; vol. 45; nb. 2; (2000); p. 272 - 275, View in Reaxys

0.01459 - 0.04563

-29 - 25

Kesemenli; Izv. Akad. Azerbajdzansk. S.S.R.; nb. 6; (1959); p. 53,54; Chem.Abstr.; (1961); p.

21714, View in Reaxys

0.01063 - 0.01488

25 - 50

Luzkii; Obuchowa; Zhurnal Fizicheskoi Khimii; vol. 31; (1957); p. 1693,1696; Chem.Abstr.; (1958); p. 6878, View in Reaxys

0.01417

30

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys; Collins; Raffel; Journal of Chemical Physics; vol. 22; (1954); p. 1728,1732, View in Reaxys

0.003 - 0.0081

20 - 140

Golik; Rawikowitsch; Zhurnal Fizicheskoi Khimii; vol. 24; (1950); p. 524,525; Chem.Abstr.; (1950); p. 8721, View in Reaxys

0.0446

Andrade; Pr. phys. Soc. London; vol. 52; (1940); p. 748,753, View in Reaxys

0.0174

15

Timmermans; Hennaut-Roland; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 29; (1932); p. 536, View in Reaxys

0.00488 - 0.02194

4.6 - 148.8

Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys

Electrical Data (17) 1 of 17

Description (Electrical Da- Dielectric relaxation time ta) Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys; Demau et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 69; (1972); p. 212,216, 217, View in Reaxys; Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys; Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 65; nb. 1; (1991); p. 47 - 51; Zhurnal Fizicheskoi Khimii; vol. 65; (1991); p. 93 - 101, View in Reaxys

2 of 17

Description (Electrical Da- Photoconductivity ta) Romanez; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 592; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1102, View in Reaxys; Trofimova; Kopylov; Russian Journal of Physical Chemistry; vol. 52; (1978); p. 1658; ; p. 2889, View in Reaxys; Kopylov; Trofimova; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 601; ; p. 1151, View in Reaxys; Kopylov et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 251,252; ; p. 481, View in Reaxys

3 of 17

Description (Electrical Da- Electrical properties ta) Madan; Canadian Journal of Physics; vol. 51; (1973); p. 1815,1817,1818, View in Reaxys

4 of 17

Description (Electrical Da- Electrical conductivity ta) Wertyporoch; Adamus; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 168; (1934); p. 31,34, 35, 40, View in Reaxys; Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 482; (1930); p. 130,138, View in Reaxys;

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Kopylev et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 1571; ; p. 2955, View in Reaxys; Ahmed et al.; Journal of Applied Chemistry; vol. 20; (1970); p. 109, View in Reaxys; Koval' et al.; Russian Journal of Physical Chemistry; vol.

46; (1972); p. 1311; ; p. 2298, View in Reaxys; Trofimova et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p.

1268; ; p. 2219, View in Reaxys; Kopylov; Yanchenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 243; ; p. 421, View in Reaxys; Kopylov et al.; Russian Journal of Physical Chemistry; vol. 39; (1965); p. 262; ; p. 491, View in Reaxys; Romanez; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 592; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1102, View in Reaxys; Kopylov; Trofimova; Sov. Phys. J. (Engl. Transl.); vol. 9; nb. 1; (1966); p. 85,53, View in Reaxys 5 of 17

Description (Electrical Da- Dielectric loss ta) Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys

6 of 17

Description (Electrical Da- Dielectric anisotropy ta) Ziolo; Piotrowska-Szczepaniak; Acta Physica Polonica; vol. 35; (1969); p. 949, View in Reaxys

7 of 17

Description (Electrical Da- Cole-Cole diagram ta) Heineken; Bruin; Physica; vol. 23; (1957); p. 57,60, View in Reaxys; Poley; Appl. scient. Res.; vol. <B> 4; (1955); p. 337,368, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys

8 of 17

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von unverduenntem und von in Paraffin geloestem Jodbenzol.

Sobhanadri; Journal of Scientific and Industrial Research; vol. 18 B; (1959); p. 508, View in Reaxys

9 of 17

Description (Electrical Da- Photoconductivity ta) Comment (Electrical Data) in Diaethylaether.

Bobyl'; Sbornik Trudov Dnepropetrovsk. inz.-stroiteln. Inst. Sonderb.; (1958); p. 3,26; Chem.Abstr.; (1961); p. 25507, View in Reaxys

10 of 17

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von in Benzol geloestem Jodbenzol.

Murty; Rao; Journal of Scientific and Industrial Research; vol. 15 B; (1956); p. 346,349; Current Science; vol. 25; (1956); p.

49, View in Reaxys

11 of 17

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von fluessigem Jodbenzol bei 21grad und Wellenlaengen von 0.802 cm bis 3.99 cm.

Poley; Appl. scient. Res.; vol. <B> 4; (1955); p. 337,368, View in Reaxys

12 of 17

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von fluessigem Jodbenzol bei 21grad und Wellenlaengen von 1.25 cm bis 3.99 cm.

Poley; Appl. scient. Res.; vol. <B> 4; (1955); p. 337,378, View in Reaxys

13 of 17

Description (Electrical Da- Dielectric relaxation time ta) Comment (Electrical Data) von in Tetrachlormethan geloestem Jodbenzol.

Hase; Zeitschrift fuer Naturforschung; vol. 8a; (1953); p. 695,703, View in Reaxys; Le Fevre; Sullivan; Journal of the Chemical Society; (1954); p. 2873,2876, View in Reaxys

14 of 17

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Loesungen von AlBr3 in Jodbenzol bei 0grad.

Wertyporoch; Adamus; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 168; (1934); p. 31,34, 35, 40, View in Reaxys

15 of 17

Description (Electrical Da- Electrical conductivity ta)

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Comment (Electrical Data) von Jodbenzol.

Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 482; (1930); p. 130,138, View in Reaxys 16 of 17

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) von Jodbenzol-Diaethylamin-Gemischen.

Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 482; (1930); p. 130,138, View in Reaxys

17 of 17

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) Jodbenzol-Anilin-Gemischen in Nitrobenzol.

Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 482; (1930); p. 130,138, View in Reaxys

Electrical Data (MCS) (1) 1 of 1

Description (Electrical Da- Dielectric constant ta (MCS)) Temperature (Electrical Data (MCS)) [°C]

80 - 110

Pressure (Electrical Data (MCS)) [Torr]

75981.1 - 186390

Partner (Electrical Data (MCS))

carbon dioxide

Leeke, Gary; Santos, Regina; Al-Duri, Bushra; Seville, Jonathan; Smith, Catherine; Holmes, Andrew B.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1370 - 1374, View in Reaxys Electrical Moment (30) 1 of 30

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

hexane

Comment (Electrical Moment)

Dipole moment (range begins): 5.9E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol.

67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 2 of 30

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

dodecane

Comment (Electrical Moment)

Dipole moment (range begins): 5.8E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol.

67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 3 of 30

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

CCl4

Comment (Electrical Moment)

Dipole moment (range begins): 5.5E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol.

67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys

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4 of 30

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

benzene

Comment (Electrical Moment)

Dipole moment (range begins): 5.7E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol.

67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 5 of 30

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

dioxane

Comment (Electrical Moment)

Dipole moment (range begins): 5.0E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol.

67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 6 of 30

Description (Electrical Moment)

Dipole moment

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

pentane

Comment (Electrical Moment)

Dipole moment (range begins): 5.8E30 C*m

Potapov, A. A.; Russian Journal of Physical Chemistry; vol. 67; nb. 11; (1993); p. 1975 - 1979; Zhurnal Fizicheskoi Khimii; vol.

67; nb. 11; (1993); p. 2193 - 2198, View in Reaxys 7 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.3

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

neat (no solvent)

Cheng, Lap-Tak; Tam, Wilson; Stevenson, Sylvia H.; Meredith, Gerald R.; Rikken, Geert; Marder, Seth R.; Journal of Physical Chemistry; vol. 95; nb. 26; (1991); p. 10631 - 10643, View in Reaxys 8 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.23

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

dioxane

Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys 9 of 30

Description (Electrical Moment)

Dipole moment

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Moment (Electrical Moment) [D]

1.36

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

CCl4

Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys 10 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.44

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

benzene

Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys 11 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.48

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

dodecane

Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys 12 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.69

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

hexane

Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys 13 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.74

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

pentane

Potapov, A. A.; Livantsova, S. A.; Sorokovikova, T. N.; Voitov, S. I.; Russian Journal of Physical Chemistry; vol. 63; nb. 1; (1989); p. 50 - 53; Zhurnal Fizicheskoi Khimii; vol. 63; (1989); p. 99 - 104, View in Reaxys 14 of 30

Description (Electrical Moment)

Dipole moment

Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys; Evans; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 609, View in Reaxys; Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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15 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (S. 572) nach Ref. 8: J. W. Smith in 'Electric Dipol Moments', Butterworths, London 1955, p.

209, 215

Colinese et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 570, View in Reaxys 16 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.39

Jain; Walker; Journal of Physical Chemistry; vol. 75; (1971); p. 2942, View in Reaxys 17 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

unverd.

Vaks; Sov. Phys. Dokl. (Engl. Transl.); vol. 12; (1967); p. 801,325, View in Reaxys 18 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

ν; p-Xylol; 15grad=1.39 D

Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys 19 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

ν; p-Xylol; 60grad=1.39 D

Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p. 2695,2699, View in Reaxys 20 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

1.38 D; ν; CCl4; 20grad; S.7

Goetz et al.; Justus Liebigs Annalen der Chemie; vol. 681; (1965); p. 1,2,8, View in Reaxys 21 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

C-H Bindung (aus IR-Intensit.)

Cole; Michell; Spectrochimica Acta; vol. 20; (1964); p. 739,742, View in Reaxys 22 of 30

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ:1.36 D (Bzl.; 30grad)

Baliah,V.; Uma,M.; Tetrahedron; vol. 19; (1963); p. 455 - 464, View in Reaxys 23 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.7

Method (Electrical Moment)

Dielectric constant (ν)

Hurdis; Smyth; Journal of the American Chemical Society; vol. 64; (1942); p. 2212,2214, View in Reaxys; Le Fevre; Rao; Australian Journal of Chemistry; vol. 8; (1955); p. 140, View in Reaxys 24 of 30

Description (Electrical Moment)

Dipole moment

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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2018-06-17 20:23:57

Moment (Electrical Moment) [D]

1.39

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

CCl4

Le Fevre; Le Fevre; Australian Journal of Chemistry; vol. 7; (1954); p. 33,35; Journal of the Chemical Society; (1954); p.

1577,1581, View in Reaxys 25 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.38

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

CCl4

Klages; Kloepping; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 57; (1953); p. 369,370, View in Reaxys 26 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.4

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

benzene

Littlejohn; Smith; Journal of the Chemical Society; (1953); p. 2456,2457, View in Reaxys 27 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.69

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

CCl4

Audsley; Goss; Journal of the Chemical Society; (1942); p. 497,498, View in Reaxys 28 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.38

Method (Electrical Moment)

Dielectric constant (ν)

Solvent (Electrical Moment)

benzene

Fuchs; Donle; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 22; (1933); p. 1,9, View in Reaxys; Tiganik; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 13; (1931); p. 425,434, View in Reaxys; Parts; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 10; (1930); p. 264,265, View in Reaxys 29 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.29

Method (Electrical Moment)

Dielectric constant (ν)

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Solvent (Electrical Moment)

benzene

Bergmann; Engel; Sandor; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 10; (1930); p. 106,119, View in Reaxys 30 of 30

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.25

Solvent (Electrical Moment)

benzene

Walden; Werner; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. <B> 2; (1929); p. 18, View in Reaxys Electrical Polarizability (2) Description (Elec- References trical Polarizability) Molar polarization

Keefe, C. Dale; Butler, Ellen; Gillis, Elizabeth; MacDonald, Jennifer L.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 1; (2007); p. 125 - 138, View in Reaxys

Optical anisotropy

Unanue,A.; Bothorel,P.; Bulletin de la Societe Chimique de France; (1964); p. 573 - 578, View in Reaxys; Le Fevre; Rao; Journal of the Chemical Society; (1958); p. 1465, View in Reaxys; Clement; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p. 626, View in Reaxys; Aroney et al.; Australian Journal of Chemistry; vol. 18; (1965); p. 1501,1504, View in Reaxys

Electrochemical Behaviour (2) Description (Elec- References trochemical Behaviour) Proton affinity

Klotz; Drost; Organic Mass Spectrometry; vol. 6; (1972); p. 647,651, View in Reaxys

Polarography

Wawzonek; Wagenknecht; Journal of Organic Chemistry; vol. 28; (1963); p. 239, View in Reaxys; Jakobson; Petrow; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk; vol. 7; (1965); p. 75,78, View in Reaxys; Zakharkin et al.; Doklady Physical Chemistry; vol. 195; (1970); p. 970,971; ; p. 1357, View in Reaxys

Electrochemical Characteristics (20) 1 of 20

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

acetonitrile

Location

supporting information

Comment (Electrochemical Characteristics)

Other electrode; potential diagram

Li, Hui; Breen, Christopher P.; Seo, Hyowon; Jamison, Timothy F.; Fang, Yuan-Qing; Bio, Matthew M.; Organic Letters; vol. 20; nb. 5; (2018); p. 1338 - 1341, View in Reaxys 2 of 20

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

toluene; acetonitrile

Location

supporting information

Comment (Electrochemical Characteristics)

Saturated calomel electrode (SCE); potential diagram; tetrabutylammonium tetrafluoroborate 0.1 M

Soria-Castro, Silvia M.; Andrada, Diego M.; Caminos, Daniel A.; Argüello, Juan E.; Robert, Marc; Peñéñory, Alicia B.; Journal of Organic Chemistry; vol. 82; nb. 21; (2017); p. 11464 - 11473, View in Reaxys 3 of 20

Description (Electrochemical Characteristics)

cyclovoltammetry

Solvent (Electrochemical Characteristics)

N,N-dimethyl-formamide

Location

supporting information

Comment (Electrochemical Characteristics)

potential diagram; 0.3 M n-Bu4NBF4

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Pichette Drapeau, Martin; Fabre, Indira; Grimaud, Laurence; Ciofini, Ilaria; Ollevier, Thierry; Taillefer, Marc; Angewandte Chemie - International Edition; vol. 54; nb. 36; (2015); p. 10587 - 10591; Angew. Chem.; vol. 127; nb. 36; (2015); p.

10733 - 10737,5, View in Reaxys 4 of 20

Description (Electrochemical Characteristics)

Electrochemical characteristics given

Beloglazkina; Mazhuga; Rakhimov; Zyk; Russian Journal of General Chemistry; vol. 80; nb. 2; (2010); p. 227 - 231, View in Reaxys 5 of 20

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Argueello, Juan E.; Penenory, Alicia B.; Journal of Organic Chemistry; vol. 68; nb. 6; (2003); p. 2362 - 2368, View in Reaxys 6 of 20

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

acetonitrile

Budnikova; Kafiyatullina; Kargin; Sinyashin; Russian Journal of General Chemistry; vol. 71; nb. 2; (2001); p. 231 - 233, View in Reaxys 7 of 20

Description (Electrochemical Characteristics)

reduction potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Temperature (Electrochemical Characteristics) [°C]

20

Enemaerke, Rasmus J.; Christensen, Torben B.; Jensen, Henrik; Daasbjerg, Kim; Journal of the Chemical Society. Perkin Transactions 2; nb. 9; (2001); p. 1620 - 1630, View in Reaxys 8 of 20

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

Potential: -2.24 V. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: 0.1 M nBu4BF4, vs. SCE

Product

iodobenzene radical anion

Pause, Laurence; Robert, Marc; Saveant, Jean-Michel; Journal of the American Chemical Society; vol. 121; nb. 30; (1999); p. 7158 - 7159, View in Reaxys 9 of 20

Description (Electrochemical Characteristics)

polarographic half-wave potential

Sease,J.W. et al.; Journal of the American Chemical Society; vol. 90; nb. 10; (1968); p. 2595 - 2598, View in Reaxys; Polievktov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 49; (1979); p. 1322,1161,1163, View in Reaxys; Fry; Krieger; Journal of Organic Chemistry; vol. 41; (1976); p. 54,55, View in Reaxys; Hussey; Diefenderfer; Journal of the American Chemical Society; vol. 89; (1967); p. 5359,5360, View in Reaxys; Suskina et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 24; (1975); p. 402; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol.

24; (1975); p. 471, View in Reaxys; Hush; Oldham; Journal of Electroanalytical Chemistry (1959-1966); vol. 6; (1963); p.

34,36, View in Reaxys; Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys; Buckels, H.-W.; Wasgestian, F.; Berichte der Bunsen-Gesellschaft; vol. 87; nb. 2; (1983); p. 154 - 158, View in Reaxys; Morlet-Savary; Wieder; Fouassier; Journal of the Chemical Society - Faraday Transactions; vol. 93; nb. 22; (1997); p. 3931 - 3937, View in Reaxys 10 of 20

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Temperature (Electrochemical Characteristics) [°C]

20

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Comment (Electrochemical Characteristics)

-2.53 V; Product: /BRN= 7804274/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: Pt electrode, Ag/AgCl/KCl, n-Bu4NBF4

Product

iodobenzene radical anion

Magdesieva; Kukhareva; Shaposhnikova; Artamkina; Beletskaya; Butin; Journal of Organometallic Chemistry; vol. 526; nb. 1; (1996); p. 51 - 58, View in Reaxys 11 of 20

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

20

Comment (Electrochemical Characteristics)

-1.86 V; Product: /BRN= 7804274/. No. of transm. electrons: 1. Method: cyclovoltammetry. Description: Hg electrode, Ag/AgCl/KCl, n-Bu4NBF4

Product

iodobenzene radical anion

Magdesieva; Kukhareva; Shaposhnikova; Artamkina; Beletskaya; Butin; Journal of Organometallic Chemistry; vol. 526; nb. 1; (1996); p. 51 - 58, View in Reaxys 12 of 20

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylsulfoxide

Temperature (Electrochemical Characteristics) [°C]

20

Comment (Electrochemical Characteristics)

-2.53 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: cyclovoltammetry. Description: Pt; Ag/AgCl; 0.05 M Bu4NBF4

Product

benzene

Magdesieva, T. V.; Kukhareva, I. I.; Artamkina, G. A.; Butin, K. P.; Beletskaya, I. P.; Journal of Organometallic Chemistry; vol. 468; nb. 1-2; (1994); p. 213 - 222, View in Reaxys 13 of 20

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

20

Comment (Electrochemical Characteristics)

-1.86 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: cyclovoltammetry. Description: Hg; Ag/AgCl; 0.05 M Bu4NBF4

Product

benzene

Magdesieva, T. V.; Kukhareva, I. I.; Artamkina, G. A.; Butin, K. P.; Beletskaya, I. P.; Journal of Organometallic Chemistry; vol. 468; nb. 1-2; (1994); p. 213 - 222, View in Reaxys 14 of 20

Description (Electrochemical Characteristics)

oxidation potential

Neikam et al.; Journal of the Electrochemical Society; vol. 111; (1964); p. 1190, View in Reaxys; Magdesieva, T.V.; Shishkin, V.N.; Butin, K.P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 11.1; (1991); p. 2400 - 2403,2227 - 2229, View in Reaxys 15 of 20

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

20

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Comment (Electrochemical Characteristics)

-1.86 V; Product: /BRN= 3587306/. No. of transm. electrons: 1. Method: voltammetry. Description: Hg cathode, silver chloride electrode as reference; 0.05 M Bu4NBF4

Product

phenyl radical

Magdesieva, T.V.; Shishkin, V.N.; Butin, K.P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 11.1; (1991); p. 2403 2405,2230 - 2232, View in Reaxys 16 of 20

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

20

Comment (Electrochemical Characteristics)

-2.55 V; Product: /BRN= 3587306/. No. of transm. electrons: 1. Method: voltammetry. Description: Pt cathode, silver chloride electrode as reference; 0.05 M Bu4NBF4

Product

phenyl radical

Magdesieva, T.V.; Shishkin, V.N.; Butin, K.P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 11.1; (1991); p. 2403 2405,2230 - 2232, View in Reaxys 17 of 20

Description (Electrochemical Characteristics)

redox potential

Amatore, Christian; Gareil, Monique; Oturan, Mehmet A.; Pinson, Jean; Saveant, Jean-Michel; Thiebault, Andre; Journal of Organic Chemistry; vol. 51; nb. 20; (1986); p. 3757 - 3761, View in Reaxys 18 of 20

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

-0.95 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: pulse polarography. Description: mercury pool cathode; 0.02 M tetramethylammonium perchlorate

Product

benzene

Mubarak, Mohammad S.; Peters, Dennis G.; Journal of Organic Chemistry; vol. 50; nb. 5; (1985); p. 673 - 677, View in Reaxys 19 of 20

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

dimethylformamide

Comment (Electrochemical Characteristics)

-0.9 V; Product: /BRN= 969212/. No. of transm. electrons: 2. Method: pulse polarography. Description: mercury pool cathode; 0.1 M tetramethylammonium perchlorate

Product

benzene

Mubarak, Mohammad S.; Peters, Dennis G.; Journal of Organic Chemistry; vol. 50; nb. 5; (1985); p. 673 - 677, View in Reaxys 20 of 20

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Colichman; Liu; Journal of the American Chemical Society; vol. 76; (1954); p. 913, View in Reaxys; v. Stackelberg; Stracke; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 53; (1949); p. 118,121, View in Reaxys; Lewin; Fodiman; Zhurnal Fizicheskoi Khimii; vol. 28; (1954); p. 601,605; Chem.Abstr.; (1954); p. 11218, View in Reaxys; Ramanthan; Subrahmanya; Proceedings - Indian Academy of Sciences, Section A; vol. <A> 47; (1958); p. 379, View in Reaxys; Gergely; Iredale; Journal of the Chemical Society; (1951); p. 13; Journal of the Chemical Society; (1953); p. 3226,3227, View in Reaxys; Colichman; Maffei; Journal of the American Chemical Society; vol. 74; (1952); p. 2744,2746, View in Reaxys Energy Data (MCS) (11) 1 of 11

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

40

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Pressure (Energy Data (MCS)) [Torr]

5250.4

Partner (Energy Data (MCS))

methanol

Atik, Z.; Meents, B.; Gmehling, J.; Journal of Chemical Thermodynamics; vol. 25; nb. 7; (1993); p. 905 - 907, View in Reaxys 2 of 11

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

water

Borisover, M. D.; Baitalov, F. D.; Solomonov, B. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 12.1; (1991); p. 2629 2638,2436 - 2443, View in Reaxys 3 of 11

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

130

Partner (Energy Data (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-propyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb.

3; (1989); p. 280 - 284, View in Reaxys 4 of 11

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

130

Partner (Energy Data (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-butyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb.

3; (1989); p. 280 - 284, View in Reaxys 5 of 11

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

130

Partner (Energy Data (MCS))

Bis(3-((4-(propoxycarbonyl)-2,3,5,6-tetrachlorobenzoyl)oxy)propyl)tetrachloroterephthalate

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb.

3; (1989); p. 280 - 284, View in Reaxys 6 of 11

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

30

Partner (Energy Data (MCS))

benzene

Otin, S.; Toledo, M. J.; Munoz, J.; Velasco, I.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 17; nb. 10; (1985); p. 935 - 940, View in Reaxys 7 of 11

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

30

Partner (Energy Data (MCS))

toluene

Otin, S.; Toledo, M. J.; Munoz, J.; Velasco, I.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 17; nb. 10; (1985); p. 935 - 940, View in Reaxys

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8 of 11

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

cyclohexane

Solomonov, B. N.; Antipin, I. S.; Novikov, V. B.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 52; nb. 12; (1982); p. 2681 - 2688,2364 - 2370, View in Reaxys 9 of 11

Description (Energy Data (MCS))

Enthalpy of solution

Fuchs; Rodewald; Journal of the American Chemical Society; vol. 95; (1973); p. 5897,5898, View in Reaxys; Fuchs et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 4705, View in Reaxys; Butler et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 1153,1157,1158, View in Reaxys; Krishnan; Friedman; Journal of Physical Chemistry; vol. 75; (1971); p. 3606, View in Reaxys; Kozlova et al.; Theoretical and Experimental Chemistry; vol. 8; (1972); p. 465; ; p. 558, View in Reaxys 10 of 11

Description (Energy Data (MCS))

Heat capacity of mixtures

Recko; Sadowska; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 17; (1969); p. 307,308, View in Reaxys 11 of 11

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

methanol

Hartley et al.; Transactions of the Faraday Society; vol. 47; (1951); p. 254,257, View in Reaxys Enthalpy of Combustion (2) Enthalpy of ComTemperature (Enbustion [Jmol-1] thalpy of Combustion) [°C]

Comment (Enthalpy of Combustion)

References

C6H5Ifluessig-> CO2Gas + H2Ofluessig + I2fest.

Smith; Acta Chemica Scandinavica (1947-1973); vol. 10; (1956); p. 884, View in Reaxys; Karlsson,K.-J.; Diss. <Lund 1941> S. 73, 79, View in Reaxys

-3.22676E+06

bei konst. Druck.

Berthelot; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 130; (1900); p. 1098; Annales de Chimie (Cachan, France); vol. <7> 21; (1900); p. 303, View in Reaxys

Enthalpy of Formation (4) Location Comment (Enthalpy of Formation)

References

-3.19578E+06

20

Enthalpy of formation given supporting informa- Enthalpy of formation tion given

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys He, Chunlin; Zhang, Jiaheng; Shreeve, Jean'Ne M.; Chemistry - A European Journal; vol. 19; nb. 23; (2013); p. 7503 - 7509, View in Reaxys Williams; Bowen; Organic Mass Spectrometry; vol. 11; (1976); p. 223,224, View in Reaxys; Speranza et al.; Journal of the American Chemical Society; vol. 99; (1977); p. 5583,5588, View in Reaxys; Halliwell; Nyburg; Journal of the Chemical Society; (1960); p. 4603,4607, View in Reaxys

Standard.

Karlsson,K.-J.; Diss. <Lund 1941> S. 73, 79, View in Reaxys

Enthalpy of Fusion (1) Enthalpy of Fusion References [Jmol-1] 9755.24

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys

Enthalpy of Vaporization (3) Enthalpy of Vapori- Temperature (Enzation [Jmol-1] thalpy of Vaporization) [°C]

References

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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42100.8

188

39983.9 49617.5

Al-Dhahir, Adnan A. Karim; Swan, Idris M.; Journal of the Indian Chemical Society; vol. 59; nb. 5; (1982); p. 645 - 653, View in Reaxys Silberman-Granowsskaja; Schugam; Zhurnal Fizicheskoi Khimii; vol. 14; (1940); p. 1004; Chem.Abstr.; (1941); p. 3867, View in Reaxys

25

Dreisbach,R.R.; Physical Properties of Chemical Compounds (= Advances in Chemistry Series Nr. 15) <Washington 1955> S. 158, View in Reaxys

Further Information (106) Description (FurReferences ther Information) Further information Korostelev et al.; Journal of Applied Spectroscopy; vol. 31; (1979); p. 1562,1564, View in Reaxys Further information Leung; Harrison; Journal of the American Chemical Society; vol. 101; (1979); p. 3168,3172, View in Reaxys Further information Kominar et al.; Canadian Journal of Chemistry; vol. 56; (1978); p. 1589, View in Reaxys Further information Bouchoux; Organic Mass Spectrometry; vol. 12; (1977); p. 681, View in Reaxys Further information Oudar et al.; Journal of Chemical Physics; vol. 67; (1977); p. 1626,1630, View in Reaxys Further information Clark; Kolb; Journal of Organic Chemistry; vol. 42; (1977); p. 359,360, View in Reaxys Further information Korostelev et al.; Journal of Applied Spectroscopy; vol. 27; (1977); p. 1487, View in Reaxys Further information Bendig; Kreysig; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 258; (1977); p. 1176, View in Reaxys Further information Nesmeyanov et al.; Doklady Physical Chemistry; vol. 231; (1976); p. 1072, View in Reaxys Further information Fry; Krieger; Journal of Organic Chemistry; vol. 41; (1976); p. 54,55, View in Reaxys Further information Baldwin et al.; Organic Mass Spectrometry; vol. 11; (1976); p. 1181,1182, View in Reaxys Further information Adler; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 427; (1976); p. 247,256, View in Reaxys Further information Levine; Bethea; Journal of Chemical Physics; vol. 63; (1975); p. 2666,2675, View in Reaxys Further information Levine; Journal of Chemical Physics; vol. 63; (1975); p. 115, View in Reaxys Further information Jen; Thomas; Journal of the American Chemical Society; vol. 97; (1975); p. 1265, View in Reaxys Further information Evans; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 609, View in Reaxys Further information Beste; Berichte der Bunsen-Gesellschaft; vol. 79; (1975); p. 54, View in Reaxys Further information Namiki et al.; Bulletin of the Chemical Society of Japan; vol. 48; (1975); p. 3073,3076,3077, View in Reaxys Further information Bitman et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 44; (1974); p. 1361,1336,1337, View in Reaxys Further information Malarski; Roczniki Chemii; vol. 48; (1974); p. 663,666, View in Reaxys Further information Wilhelm; Journal of Chemical Physics; vol. 58; (1973); p. 3558,3559, View in Reaxys Further information Karasek et al.; Analytical Chemistry; vol. 45; (1973); p. 1210,1213, View in Reaxys Further information Berthelot et al.; Journal of Molecular Structure; vol. 18; (1973); p. 435,441, View in Reaxys Further information Keruzore; Labarre; Tetrahedron; vol. 29; (1973); p. 2925, View in Reaxys Further information Bock,H. et al.; Chemische Berichte; vol. 105; (1972); p. 3850 - 3864, View in Reaxys Further information Bhagvanth Rao et al.; Journal of the Indian Institute of Science; vol. 53; (1971); p. 99,103, View in Reaxys Further information Thosar et al.; Indian Journal of Pure and Applied Physics; vol. 9; (1971); p. 1009, View in Reaxys Further information Peschel; Schnorrer; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 75; (1971); p. 96,101, 104, 105, 109, View in Reaxys Further information Navmenko et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p. 2533,2562, View in Reaxys Further information Baker; Turner; Philosophical Transactions of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 268; (1970); p. 131,136, View in Reaxys Further information Davies et al.; Transactions of the Faraday Society; vol. 66; (1970); p. 273,291, View in Reaxys Further information Sergeev et al.; Optics and Spectroscopy; vol. 29; (1970); p. 63; ; p. 119, View in Reaxys Further information Myasishcheva et al.; High Energy Chemistry; vol. 4; (1970); p. 398; ; p. 447, View in Reaxys

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Further information Howe; Williams; Journal of the American Chemical Society; vol. 91; (1969); p. 7137,7141, View in Reaxys Further information Facchetti et al.; Chimica e l'Industria (Milan, Italy); vol. 51; (1969); p. 1373, View in Reaxys Further information Masson; Thuillier; Bulletin de la Societe Chimique de France; (1969); p. 4368,4369,4374,4375, View in Reaxys Further information Warman et al.; Journal of Chemical Physics; vol. 51; (1969); p. 3477, View in Reaxys Further information Steelhammer; Wentworth; Journal of Chemical Physics; vol. 51; (1969); p. 1802,1804,1809, View in Reaxys Further information Recko; Sadowska; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 17; (1969); p.

307,308, View in Reaxys Further information Lecomte; Bulletin de la Societe Chimique de France; (1969); p. 2215,2224, View in Reaxys Further information Hartmann; Schmidt; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 62; (1968); p. 312, View in Reaxys Further information Persky et al.; Journal of Chemical Physics; vol. 49; (1968); p. 2347,2353, View in Reaxys Further information Hartmann; Schmidt; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 875, View in Reaxys Further information Cantacuzene; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 65; (1968); p. 516, View in Reaxys Further information Zuelfuegarzade et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 239; (1968); p. 425, View in Reaxys Further information Langer et al.; Journal of Physical Chemistry; vol. 72; (1968); p. 4020, View in Reaxys Further information Caldwell; Hacobian; Australian Journal of Chemistry; vol. 21; (1968); p. 1,5,6, View in Reaxys Further information Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 28; (1968); p. 89,97, View in Reaxys Further information Lisitsa; Ralko; Optics and Spectroscopy; vol. 24; (1968); p. 284; ; p. 540, View in Reaxys Further information Imanow et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 238; (1968); p. 133, View in Reaxys Further information Huang; Sullivan; Australian Journal of Chemistry; vol. 21; (1968); p. 1721,1723, View in Reaxys Further information Cercek; Journal of Physical Chemistry; vol. 72; (1968); p. 3832, View in Reaxys Further information Rodgers et al.; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 253, View in Reaxys Further information Caldwell; Hacobian; Australian Journal of Chemistry; vol. 21; (1968); p. 1403,1409,1410, View in Reaxys Further information Gragerow; Kasuchim; J. Gen. Chem. USSR (Engl. Transl.); vol. 38; (1968); p. 2393,2317, View in Reaxys Further information Dumas et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 267; (1968); p. 267, View in Reaxys Further information Sease,J.W. et al.; Journal of the American Chemical Society; vol. 90; nb. 10; (1968); p. 2595 - 2598, View in Reaxys Further information Cann; Biochemistry; vol. 6; (1967); p. 3435,3436 - 3437, View in Reaxys Further information Cosandey; Lerch; Helvetica Chimica Acta; vol. 50; (1967); p. 2215, View in Reaxys Further information Stamouli; Katsanos; Radiochimica Acta; vol. 7; (1967); p. 177, View in Reaxys Further information Marchetti; Rearns; Journal of the American Chemical Society; vol. 89; (1967); p. 5335, View in Reaxys Further information Petrosjan; Reutow; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1967); p. 1311; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1967); p. 1361, View in Reaxys Further information Voronkov et al.; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 2; (1966); p. 5,8; Khimiya Geterotsiklicheskikh Soedinenii; vol. 2; (1966); p. 8, View in Reaxys Further information Christophorou et al.; Journal of Chemical Physics; vol. 45; (1966); p. 536, View in Reaxys Further information Baron; Lumbroso-Bader; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 63; (1966); p. 1416, View in Reaxys Further information Kopylow et al.; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 207; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 389, View in Reaxys Further information Olszer; Siekierski; Journal of Inorganic and Nuclear Chemistry; vol. 28; (1966); p. 1991, View in Reaxys Further information Kerr et al.; Molecular Physics; vol. 10; (1966); p. 14, View in Reaxys Further information Brownlee et al.; Journal of the American Chemical Society; vol. 88; (1966); p. 1413,1415, 1416, View in Reaxys Further information Prakash; Pandey; Tetrahedron; vol. 21; (1965); p. 2717, View in Reaxys Further information Lepley; Giumanini; Chimica e l'Industria (Milan, Italy); vol. 47; (1965); p. 408, View in Reaxys

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Further information Smith; Kollmansberger; Journal of Physical Chemistry; vol. 69; (1965); p. 4159, View in Reaxys Further information Zhdanov; Doklady Chemistry; vol. 162; (1965); p. 603,604; Doklady Akademii Nauk SSSR; vol. 162; (1965); p. 1314, View in Reaxys Further information Beringer,F.M.; Falk,R.A.; Journal of the Chemical Society; (1964); p. 4442 - 4451, View in Reaxys Further information Griffiths; Derwish; Journal of Molecular Spectroscopy; vol. 13; (1964); p. 393,397, View in Reaxys Further information Lerch; Cosandey; Helvetica Chimica Acta; vol. 47; (1964); p. 2417; Chem.Abstr.; vol. 56; nb. 9393; (1962), View in Reaxys Further information Porter; Ward; Proceedings of the Chemical Society, London; (1964); p. 288, View in Reaxys Further information Voigt; Reid; Journal of the American Chemical Society; vol. 86; (1964); p. 3930,3932, View in Reaxys Further information Voigt; Journal of the American Chemical Society; vol. 86; (1964); p. 3611,3614, View in Reaxys Further information Dearden; Journal of Organic Chemistry; vol. 29; (1964); p. 1821,1825, View in Reaxys Further information Delorme; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 61; (1964); p. 1439,1449, 1453, View in Reaxys Further information Schwetlick; Pietzsch; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 125,127, View in Reaxys Further information Applequist; O'Brien; Journal of the American Chemical Society; vol. 85; (1963); p. 743,747, View in Reaxys Further information Bryce-Smith et al.; Proceedings of the Chemical Society, London; (1963); p. 219, View in Reaxys Further information Marckmann et al.; Berichte der Bunsen-Gesellschaft; vol. 67; (1963); p. 33, View in Reaxys Further information WILLEMART; ROBIN; Annales pharmaceutiques françaises; vol. 21; (1963); p. 423 - 424, View in Reaxys Further information Garst; Cole; Tetrahedron Letters; (1963); p. 679,681, View in Reaxys Further information Imanov; Zul'fugarzade; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 188; ; p. 366, View in Reaxys Further information Schindlbauer; Monatshefte fuer Chemie; vol. 94; (1963); p. 99,105, View in Reaxys Further information Kuester; Zeitschrift fuer Elektrochemie; vol. 66; (1962); p. 273,275, View in Reaxys Further information Srivastavan; Lal; Journal of Scientific and Industrial Research, Section B: Physical Sciences; vol. 21; (1962); p. 86, View in Reaxys Further information Kropp; Burton; Journal of Chemical Physics; vol. 37; (1962); p. 1742,1746, View in Reaxys Further information Barton; Serebryakov; Proceedings of the Chemical Society, London; (1962); p. 309, View in Reaxys Further information Thompson et al.; Analytical Chemistry; vol. 34; (1962); p. 154, View in Reaxys Further information Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys Further information Schmid; Zeitschrift fuer Elektrochemie; vol. 66; (1962); p. 53, View in Reaxys Further information McLafferty; Analytical Chemistry; vol. 34; (1962); p. 16,23, View in Reaxys Further information Lauterbur; Tetrahedron Letters; (1961); p. 274,276, View in Reaxys Further information Ormrod; Hogg; Journal of Chemical Physics; vol. 34; (1961); p. 624,625, View in Reaxys Further information Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 126, View in Reaxys Further information Bloor; Canadian Journal of Chemistry; vol. 39; (1961); p. 2256,2259, View in Reaxys Further information Hatcher; Journal of Chemical Physics; vol. 35; (1961); p. 2266, View in Reaxys Further information Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 91, View in Reaxys Further information Bardamowa; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR; vol. 2; (1960); p. 71,72,73, View in Reaxys Further information Sharefkin; Schwerz; Analytical Chemistry; vol. 32; (1960); p. 996, View in Reaxys Further information Halliwell; Nyburg; Journal of the Chemical Society; (1960); p. 4603,4607, View in Reaxys Heat Capacity Cp (2) Heat Capacity Cp Temperature (Heat [Jmol-1K-1] Capacity Cp) [°C]

References

54.05 - 160.86

Stull; Journal of the American Chemical Society; vol. 59; (1937); p. 2726,2729, View in Reaxys

-183.2 - 46.8

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55.27 - 112.21

-192.2 - -47.1

Interatomic Distances and Angles (3) Description Comment (Interatomic Distances and Angles)

Aoyama; Kanda; Sci. Rep. Tohoku Univ., Ser. 1: Phys., Chem., Astron.; vol. # 24; (1935); p.

116,120, View in Reaxys References

Interatomic distances and angles

Joliet; Berthon; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol.

260; (1965); p. 2805, View in Reaxys; Ugolini, R.; Diehl, P.; Journal of Molecular Structure; vol.

216; (1990); p. 325 - 332, View in Reaxys

Electron distribution

Kanekar et al.; Proceedings - Indian Academy of Sciences, Section A; vol. 65; (1967); p.

353,356, View in Reaxys; Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 16; nb. 7; (1968); p. 1187, View in Reaxys

Interatomic distances and angles

aus dem RoentgenDiagramm des Dampfes ermittelt.

Ionization Potential (15) Ionization Potential Method (Ionization [eV] Potential)

Schoppe; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 34; (1936); p. 461,465, 469, View in Reaxys; Kratky; Worthmann; Monatshefte fuer Chemie; vol. 76; (1947); p. 263,273, 275, View in Reaxys Comment (Ionization Potential)

References

16.83

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

15.48

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

15.12

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

14.42

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

13.63

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

12.6

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

11.64

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

11.54

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

9.74

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

9.49

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

8.75

PE

Type: vertical.

Higher potentials: 16.83 eV

Imura, Kohei; Kishimoto, Naoki; Ohno, Koichi; Journal of Physical Chemistry A; vol. 105; nb. 17; (2001); p. 4189 - 4199, View in Reaxys

8.79

PE

Type: vertical.

Fujisawa, S.; Ohno, K.; Masuda, S.; Harada, Y.; Journal of the American Higher potentials: Chemical Society; vol. 108; nb. 21; (1986); p. 6505 - 6511, View in Reaxys 9.53, 9.77, 10.58, 11.62, 12.39, 12.7, 13.62, 14.30, 15.03, 15.5, 16.70 eV Baker; Turner; Philosophical Transactions of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 268;

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(1970); p. 131,136, View in Reaxys; Walkley; Journal of Chemical Physics; vol. 33; (1960); p. 621, View in Reaxys; Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys; Gibson; Canadian Journal of Chemistry; vol. 51; (1973); p.

3065,3066, View in Reaxys; Jen; Thomas; Journal of the American Chemical Society; vol. 97; (1975); p. 1265, View in Reaxys; Boschi; Salahub; Canadian Journal of Chemistry; vol. 52; (1974); p. 1217,1220, View in Reaxys; Yeo; Williams; Journal of the Chemical Society [Section] D: Chemical Communications; (1970); p. 886, View in Reaxys; Baldwin et al.; Organic Mass Spectrometry; vol. 11; (1976); p. 1181,1182, View in Reaxys; Bendig; Kreysig; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 258; (1977); p. 1176, View in Reaxys; Sell; Kuppermann; Chemical Physics; vol. 33; (1978); p. 367, View in Reaxys; Momigny et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 1; (1968); p. 53,55, 56, 59, 60, 62, View in Reaxys; Malarski; Roczniki Chemii; vol.

48; (1974); p. 663,666, View in Reaxys; Adler; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 427; (1976); p. 247,256, View in Reaxys; Baker et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 22, View in Reaxys 8.73

Photoionization

Watanabe; Journal of Chemical Physics; vol. 26; (1957); p. 542,543; Journal of Chemical Physics; vol. 22; (1954); p. 1564,1566, View in Reaxys

9.1

Electron impact

Morrison; Nicholson; Journal of Chemical Physics; vol. 20; (1952); p.

1021, View in Reaxys

Liquid Phase (2) Description (Liquid References Phase) Radial distribution function

Brunvoll, Jon; Samdal, Svein; Thomassen, Hanne; Vilkov, Lev V.; Volden, Hans V.; Acta Chemica Scandinavica; vol. 44; nb. 1; (1990); p. 23 - 30, View in Reaxys

Liquid-crystalline properties

Haloui et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 72; (1975); p. 1097, View in Reaxys

Liquid/Liquid Systems (MCS) (16) 1 of 16

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

Shiflett, Mark B.; Niehaus, Anne Marie S.; Yokozeki; Journal of Chemical and Engineering Data; vol. 54; nb. 7; (2009); p.

2090 - 2094, View in Reaxys 2 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

69.99 - 109.99

Partner (Liquid/Liquid Systems (MCS))

1-Hexadecanol; air

Xiao, Hang; Lei, Ying Duan; Wania, Frank; Journal of Chemical and Engineering Data; vol. 51; nb. 2; (2006); p. 338 - 346, View in Reaxys 3 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

aq. phosphate buffer

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

30

Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate; H2O

Khaledi; Kelly; Burns; Analytical Chemistry; vol. 73; nb. 24; (2001); p. 6057 - 6062, View in Reaxys 4 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS))

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Solvent (Liquid/Liquid Systems (MCS))

H2O; gas

Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

sodium dodecyl-sulfate

Bel'skii; Russian Chemical Bulletin; vol. 49; nb. 2; (2000); p. 251 - 255, View in Reaxys 5 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

benzene; hexane

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25

Partner (Liquid/Liquid Systems (MCS))

Porous sol-gel silica glass

Badjic, Jovica D.; Kostic, Nenad M.; Journal of Physical Chemistry B; vol. 104; nb. 47; (2000); p. 11081 - 11087, View in Reaxys 6 of 16

Description (Liquid/Liquid Solution equilibrium Systems (MCS)) Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys 7 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Comment (Liquid/Liquid Systems (MCS))

equation

Partner (Liquid/Liquid Systems (MCS))

chloroform

Abraham, Michael H.; Platts, James A.; Hersey, Anne; Leo, Albert J.; Taft, Robert W.; Journal of Pharmaceutical Sciences; vol. 88; nb. 7; (1999); p. 670 - 679, View in Reaxys 8 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

gas

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

39.2

Partner (Liquid/Liquid Systems (MCS))

apolane

Weckwerth, Jeff D.; Carr, Peter W.; Vitha, Mark F.; Nasehzadeh, Asad; Analytical Chemistry; vol. 70; nb. 17; (1998); p.

3712 - 3716, View in Reaxys 9 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

24.9

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Partner (Liquid/Liquid Systems (MCS))

2-{2-[4-(1,1,3,3-tetramethyl-butyl)-phenoxy]-ethoxy}-ethanol

Suslov, D. A.; Solomonov, B. N.; Russian Journal of Physical Chemistry; vol. 69; nb. 7; (1995); p. 1140 - 1143; Zhurnal Fizicheskoi Khimii; vol. 69; nb. 7; (1995); p. 1264 - 1267, View in Reaxys 10 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

Hexadecane; water

Abraham, Michael H.; Whiting, Gary S.; Fuchs, Richard; Chambers, Eric J.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 2; (1990); p. 291 - 300, View in Reaxys 11 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

19.9

Partner (Liquid/Liquid Systems (MCS))

octanol; water

Kramer, C. R.; Henze, U.; Schelenz, Th.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 271; nb. 6; (1990); p. 1155 1167, View in Reaxys 12 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Partner (Liquid/Liquid Systems (MCS))

octanol

Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Marcus, Yizhak; Taft, Robert W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5244 - 5255, View in Reaxys; Yalkowsky; Valvani; Journal of Pharmaceutical Sciences; vol. 69; nb. 8; (1980); p. 912 - 922, View in Reaxys 13 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Solvent (Liquid/Liquid Systems (MCS))

H2O

Temperature (Liquid/ Liquid Systems (MCS)) [°C]

25

Partner (Liquid/Liquid Systems (MCS))

octanol

Tewari, Yadu B.; Miller, Michele M.; Wasik, Stanley P.; Martire, Daniel E.; Journal of Chemical & Engineering Data; vol.

27; nb. 4; (1982); p. 451 - 454, View in Reaxys; Leahy; Journal of pharmaceutical sciences; vol. 75; nb. 7; (1986); p. 629 - 636, View in Reaxys 14 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

35

Partner (Liquid/Liquid Systems (MCS))

octanol; H2O

Garst; Wilson; Journal of Pharmaceutical Sciences; vol. 73; nb. 11; (1984); p. 1616 - 1623, View in Reaxys 15 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Partner (Liquid/Liquid Systems (MCS))

octanol; H2O

Garst; Journal of Pharmaceutical Sciences; vol. 73; nb. 11; (1984); p. 1623 - 1629, View in Reaxys

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16 of 16

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Niclas; Kollecker; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 16; (1976); p. 367, View in Reaxys; Korenman et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 683,726, View in Reaxys

Liquid/Solid Systems (MCS) (10) 1 of 10

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

benzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 2 of 10

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

fluorobenzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 3 of 10

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

chlorobenzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 4 of 10

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Partner (Liquid/Solid Systems (MCS))

bromobenzene

Penkala; Roczniki Chemii; vol. 27; (1953); p. 267,268; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III>1; (1953); p. 151,152, View in Reaxys 5 of 10

Description (Liquid/Solid Systems (MCS))

Melting diagram

Solvent (Liquid/Solid Sys- benzene tems (MCS)) Klemm; Klemm; Schiemann; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 165; (1933); p. 379,386, View in Reaxys 6 of 10

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-60.5

Partner (Liquid/Solid Systems (MCS))

fluorobenzene

Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys 7 of 10

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-51.5

Partner (Liquid/Solid Systems (MCS))

fluorobenzene

Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys 8 of 10

Description (Liquid/Solid Systems (MCS))

Eutectic

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Temperature (Liquid/Solid Systems (MCS)) [°C]

-36.5

Partner (Liquid/Solid Systems (MCS))

fluorobenzene

Pascal; Bulletin de la Societe Chimique de France; vol. <4> 13; (1913); p. 745, View in Reaxys 9 of 10

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-45

Partner (Liquid/Solid Systems (MCS))

antimony(III) chloride

Menschutkin; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 419,422; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 380, View in Reaxys 10 of 10

Description (Liquid/Solid Systems (MCS))

Eutectic

Temperature (Liquid/Solid Systems (MCS)) [°C]

-32

Partner (Liquid/Solid Systems (MCS))

antimony(III) bromide

Menschutkin; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 43; (1911); p. 419,422; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 380, View in Reaxys Liquid/Vapour Systems (MCS) (13) 1 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

24.9

Partner (Liquid/Vapour Systems (MCS))

2-{2-[4-(1,1,3,3-tetramethyl-butyl)-phenoxy]-ethoxy}-ethanol

Suslov, D. A.; Solomonov, B. N.; Russian Journal of Physical Chemistry; vol. 69; nb. 7; (1995); p. 1140 - 1143; Zhurnal Fizicheskoi Khimii; vol. 69; nb. 7; (1995); p. 1264 - 1267, View in Reaxys 2 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

130

Partner (Liquid/Vapour Systems (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-propyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb.

3; (1989); p. 280 - 284, View in Reaxys 3 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

130

Partner (Liquid/Vapour Systems (MCS))

O,O"-1,3-Propanediyl O',O'''-di-n-butyl bis(tetrachloroterephthalate)

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb.

3; (1989); p. 280 - 284, View in Reaxys 4 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

130

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Partner (Liquid/Vapour Systems (MCS))

Bis(3-((4-(propoxycarbonyl)-2,3,5,6-tetrachlorobenzoyl)oxy)propyl)tetrachloroterephthalate

Coca, Jose; Rodriguez, Jorge L.; Medina, Ignacio; Langer, Stanley H.; Journal of Chemical & Engineering Data; vol. 34; nb.

3; (1989); p. 280 - 284, View in Reaxys 5 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

25

Partner (Liquid/Vapour Systems (MCS))

octane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 6 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

25

Partner (Liquid/Vapour Systems (MCS))

butanone

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 7 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

25

Partner (Liquid/Vapour Systems (MCS))

ethanol

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 8 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

25

Partner (Liquid/Vapour Systems (MCS))

toluene

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 9 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

25

Partner (Liquid/Vapour Systems (MCS))

1,4-dioxane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 10 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Temperature (Liquid/ Vapour Systems (MCS)) [°C]

25

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Partner (Liquid/Vapour Systems (MCS))

nitromethane

Park, Jung Hag; Hussam, Abul; Couasnon, Pascal; Fritz, David; Carr, Peter W.; Analytical Chemistry; vol. 59; nb. 15; (1987); p. 1970 - 1976, View in Reaxys 11 of 13

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Dowell; Stewart; Phosphorus and Sulfur and the Related Elements; vol. 1; (1976); p. 135,137, View in Reaxys; Langer; Purnell; Journal of Physical Chemistry; vol. 67; (1963); p. 263,265,266, View in Reaxys 12 of 13

Description (Liquid/ Vapour Systems (MCS))

Boiling point diagram

Solvent (Liquid/Vapour Systems (MCS))

chlorobenzene; bromobenzene

Miller; Bulletin des Societes Chimiques Belges; vol. 50; (1941); p. 51,55, View in Reaxys 13 of 13

Description (Liquid/ Vapour Systems (MCS))

Boiling point diagram

Comment (Liquid/Vapour Systems (MCS))

unter verschiedenen Drucken.

Feitler; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 4; (1889); p. 72, View in Reaxys; Young; Journal of the Chemical Society; vol. 55; (1889); p. 501; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 422, View in Reaxys Magnetic Data (1) Description (Magnetic Data)

References

Magnetic properties Bruniquel et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 70; (1973); p. 1558, View in Reaxys Magnetic Susceptibility (1) References Baliah; Srinivasan; Indian Journal of Chemistry; vol. 9; (1971); p. 215, View in Reaxys; Le Fevre; Murthy; Australian Journal of Chemistry; vol. 19; (1966); p. 1315,1316,1320, View in Reaxys; Le Fevre; Murthy; Australian Journal of Chemistry; vol. 19; (1966); p. 179,182, View in Reaxys; Bonnafous et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 462, View in Reaxys Mechanical & Physical Properties (MCS) (8) 1 of 8

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

32

Partner (Mechanical & Physical Properties (MCS))

1-methyl-pyrrolidin-2-one

Zainel, Hanaa A.; Al-Azzawi, Souad F.; Swellem, Hassan I.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 84; nb. 10; (1988); p. 3511 - 3516, View in Reaxys 2 of 8

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

N,N-dimethyl-formamide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 3 of 8

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

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Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

dimethyl sulfoxide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 4 of 8

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

acetonitrile

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 5 of 8

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

CCl4

Shahidi, Fereidoon; Canadian Journal of Chemistry; vol. 61; (1983); p. 1414 - 1416, View in Reaxys 6 of 8

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Recko; Sadowska; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 17; (1969); p. 307,308, View in Reaxys 7 of 8

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

25

Partner (Mechanical & Physical Properties (MCS))

benzene

Luzkii et al.; Zhurnal Obshchei Khimii; vol. 28; (1958); p. 2386,2390; engl. Ausg. S. 2423, 2427, View in Reaxys 8 of 8

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Temperature (Mechanical & Physical Properties (MCS)) [°C]

50

Partner (Mechanical & Physical Properties (MCS))

benzene

Luzkii et al.; Zhurnal Obshchei Khimii; vol. 28; (1958); p. 2386,2390; engl. Ausg. S. 2423, 2427, View in Reaxys Mechanical Properties (4) Description (MeReferences chanical Properties)

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Molar volume

Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys; Narbutt; Siekierski; Roczniki Chemii; vol. 48; (1974); p. 1777,1781, View in Reaxys; Chawla, B.; Mehta, S. K.; Jasra, R. V.; Suri, S. K.; Canadian Journal of Chemistry; vol. 61; (1983); p. 2147 - 2150, View in Reaxys; Carr; Doherty; Kamlet; Taft; Melander; Horvath; Analytical Chemistry; vol. 58; nb. 13; (1986); p. 2674 - 2680, View in Reaxys; Leahy; Journal of pharmaceutical sciences; vol. 75; nb. 7; (1986); p. 629 - 636, View in Reaxys

Viscosity

Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Singh; Singh; Journal of the Indian Chemical Society; vol. 55; (1978); p. 738, View in Reaxys; Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p. 330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys; Ertl; Dullien; AIChE Journal; vol. 19; (1973); p. 1215,1218, View in Reaxys

Compressibility

Bobyl et al.; Sov. Phys. J. (Engl. Transl.); vol. 6; (1965); p. 48,30, View in Reaxys

Volume change on melting

Schinke; Sauerwald; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 216; (1961); p. 26,31, View in Reaxys

Molecular Deformation (3) Description (MoComment (Molecu- References lecular Deformalar Deformation) tion) Fundamental vibrations

Cole; Michell; Spectrochimica Acta; vol. 20; (1964); p. 739,742, View in Reaxys; Griffiths; Thompson; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 298; (1967); p. 51,54, View in Reaxys; Koeser, Heinz J. K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 2; (1984); p. 125 136, View in Reaxys

Force constants

Becher; Hoefler; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol.

25; (1969); p. 1703,1705, View in Reaxys; Korostelev et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1538; ; p. 2682, View in Reaxys

Fundamental vibra- des Molekuels. tions

Plyler; Allen; Tidwell; Journal of Research of the National Bureau of Standards (United States); vol. 58; (1957); p. 255,256, 260, View in Reaxys; Whiffen; Journal of the Chemical Society; (1956); p. 1350, View in Reaxys

Optical Rotatory Dispersion (1) References Haberditzl; Koeppel; Z. Naturforsch., B: Anorg. Chem., Org. Chem., Biochem., Biophys.,; vol. 22; (1967); p. 691, View in Reaxys Optics (11) Description (Optics)

Comment (Optics)

References

Rayleigh scattering

Atakhodzhaev, A. K.; Malomuzh, N. P.; Faizullaev, Sh. F.; Journal of Applied Spectroscopy; vol. 54; nb. 1; (1991); p. 23 - 28; Zhurnal Prikladnoi Spektroskopii; vol. 54; nb. 1; (1991); p. 33 39, View in Reaxys; Friedman, J. S.; She, C. Y.; Journal of Chemical Physics; vol. 99; nb. 7; (1993); p. 4960 - 4969, View in Reaxys

Linear dichroism

Jede, F.; Stratmann, A. W.; Schrader, B.; Molecular Crystals and Liquid Crystals (1969-1991); vol. 140; (1986); p. 297 - 302, View in Reaxys

Magnetorotation

Murthy; Naidu; Current Science; vol. 48; (1979); p. 292, View in Reaxys

Degree of depolarization of Rayleigh scattering

Clement; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 75; (1978); p.

747,748, 752, View in Reaxys

Magnetic circular dichroism

Shieh et al.; Journal of Physical Chemistry; vol. 77; (1973); p. 1031,1035, 1036, View in Reaxys; Foss; McCarville; Journal of the American Chemical Society; vol. 89; (1967); p. 30, View in Reaxys

Magnetic birefringence (CottonMouton effect)

Cotton; Mouton; Annales de Chimie (Cachan, France); vol. <8> 19; (1910); p. 175; Annales de Chimie (Cachan, France); vol. <8> 28; (1913); p. 215, View in Reaxys; Le Fevre et al.; Australian Journal of Chemistry; vol. 24; (1971); p. 1177,1180, View in Reaxys; Le Fevre; Murthy; Australian Journal of Chemistry; vol. 19; (1966); p. 1315,1316,1320, View in Reaxys

Electric birefringence (Kerr effect)

Leiser; Abh. Dtsch. Bunsen-Ges.; nb. 4; (1910); p. 69; Chem. Zentralbl.; vol. 82; nb. I; (1911); p.

622, View in Reaxys; Okabayashi; Bulletin of the Chemical Society of Japan; vol. 34; (1961); p.

1010,1012, View in Reaxys

Electric birefringence (Kerr effect)

an Loesungen in CCl4 ermittelt.

Otterbein; Phys. Z.; vol. 35; (1934); p. 249,264, View in Reaxys

Mechanical birefringence

bei 17grad.

Vorlaender; Fischer; Chemische Berichte; vol. 65; (1932); p. 1756,1759, View in Reaxys

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Electric birefringence (Kerr effect)

Jodbenzol zeigt positive elektrische Doppelbrechung.

Schmidt; Ann. d. Physik; vol. <4> 7; (1902); p. 165, View in Reaxys

Magnetorotation

Magnetisches Drehungsvermoegen.

Perkin; Journal of the Chemical Society; vol. 69; (1896); p. 1241; Journal of the Chemical Society; vol. 77; (1900); p. 278, View in Reaxys

Other Thermochemical Data (6) Description (Other Comment (Other Thermochemical Thermochemical Data) Data)

References

Thermodynamic properties

Pac et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 1169,1171, View in Reaxys; Butler; Lielmezs; Journal of Chemical and Engineering Data; vol. 14; (1969); p.

335,336, View in Reaxys; Langer; Parnell; Journal of Physical Chemistry; vol. 70; (1966); p.

904, View in Reaxys; Wilhelm; Battino; Journal of Chemical Physics; vol. 55; (1971); p.

4012,4014, View in Reaxys

Entropy

Castro,C.E. et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 6464 - 6470, View in Reaxys; Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys

Enthalpy

Castro,C.E. et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 6464 - 6470, View in Reaxys; Krishnan; Friedman; Journal of Physical Chemistry; vol. 73; (1969); p. 1572, View in Reaxys

Cryoscopic constant

Kryoskopisches Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 482; (1930); p. 130,138, Verhalten von Jod- View in Reaxys benzol in Nitrobenzol und in Dioxan.

Cryoscopic constant

Kryoskopisches Verhalten von Jodbenzol-AnilinGemischen in Dioxan.

Heat of combustion Molekulare Verat constant volume brennungswaerme: 770.0 kcal.

Meisenheimer; Dorner; Justus Liebigs Annalen der Chemie; vol. 482; (1930); p. 130,138, View in Reaxys

Berthelot; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 130; (1900); p. 1098; Annales de Chimie (Cachan, France); vol. <7> 21; (1900); p. 303, View in Reaxys

Partition octan-1-ol/water (MCS) (2) 1 of 2

log POW

3.2

Patent; MICAP PLC; WO2005/102045; (2005); (A1) English, View in Reaxys 2 of 2

log POW

3.25

Schultz, T. Wayne; Chemical Research in Toxicology; vol. 12; nb. 12; (1999); p. 1262 - 1267, View in Reaxys Self-diffusion (1) References Ertl; Dullien; AIChE Journal; vol. 19; (1973); p. 1215,1218, View in Reaxys Solubility (MCS) (17) 1 of 17

Solubility [g·l-1]

0.07

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

25

Solvent (Solubility (MCS))

water

Potier, Jonathan; Menuel, Stephane; Rousseau, Jolanta; Tumkevicius, Sigitas; Hapiot, Frederic; Monflier, Eric; Applied Catalysis A: General; vol. 479; (2014); p. 1 - 8, View in Reaxys 2 of 17

Comment (Solubility (MCS))

insoluble in water

Firouzabadi, Habib; Iranpoor, Nasser; Ghaderi, Arash; Gholinejad, Mohammad; Rahimi, Sajjad; Jokar, Safura; RSC Advances; vol. 4; nb. 53; (2014); p. 27674 - 27682, View in Reaxys 3 of 17

Saturation

in pure solvent

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Comment (Solubility (MCS))

temperature dependence. Object(s) of Study: pressure dependence. Object(s) of Study: diagram

Leeke, Gary; Santos, Regina; Al-Duri, Bushra; Seville, Jonathan; Smith, Catherine; Holmes, Andrew B.; Journal of Chemical and Engineering Data; vol. 50; nb. 4; (2005); p. 1370 - 1374, View in Reaxys 4 of 17

Saturation

in pure solvent

Comment (Solubility (MCS))

equation

Ruelle, Paul; Kesselring, Ulrich W.; Journal of Pharmaceutical Sciences; vol. 87; nb. 8; (1998); p. 998 - 1014, View in Reaxys; Jain, Neera; Yalkowsky, Samuel H.; Journal of Pharmaceutical Sciences; vol. 90; nb. 2; (2001); p. 234 - 252, View in Reaxys 5 of 17

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

25

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

Solubility 1.66E-3 mol/l

Sanemasa, Isao; Wu, Ji-Shi; Toda, Kei; Bulletin of the Chemical Society of Japan; vol. 70; nb. 2; (1997); p. 365 - 369, View in Reaxys 6 of 17

Solubility [g·l-1]

0.201

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

25

Solvent (Solubility (MCS))

H2O

Tewari, Yadu B.; Miller, Michele M.; Wasik, Stanley P.; Martire, Daniel E.; Journal of Chemical & Engineering Data; vol.

27; nb. 4; (1982); p. 451 - 454, View in Reaxys 7 of 17

Saturation

in pure solvent

Valvani; Yalkowsky; Roseman; Journal of Pharmaceutical Sciences; vol. 70; nb. 5; (1981); p. 502 - 507, View in Reaxys; Yalkowsky; Valvani; Journal of Pharmaceutical Sciences; vol. 69; nb. 8; (1980); p. 912 - 922, View in Reaxys 8 of 17

Comment (Solubility (MCS))

in H20

Nelson; Smit; South African Journal of Chemistry; vol. 31; (1978); p. 76, View in Reaxys 9 of 17

Comment (Solubility (MCS))

in Wasser

Vesala; Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry; vol. 28; (1974); p. 839,841, View in Reaxys 10 of 17

Comment (Solubility (MCS))

Loesl.-Parameter

Narbutt; Siekierski; Roczniki Chemii; vol. 48; (1974); p. 1777,1781, View in Reaxys 11 of 17

Comment (Solubility (MCS))

W. bei 20grad

Prakash; Pandey; Tetrahedron; vol. 21; (1965); p. 903, View in Reaxys 12 of 17

Comment (Solubility (MCS))

Loeslichkeits-Best. v. W. in C6H5I bei verschied. Temp. in Gegw. v. HTO durch Scintillationszahlung (Tab.)

Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys 13 of 17

Comment (Solubility (MCS))

in 104 ml C6H5I loesen sich bei 25grad: 4.9 ml W.

Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys 14 of 17

Comment (Solubility (MCS))

in 104 ml C6H5I loesen sich bei 30grad: 5.6 ml W.

Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys

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15 of 17

Comment (Solubility (MCS))

in 104 ml C6H5I loesen sich bei 35grad: 6.3 ml W.

Jones; Monk; Journal of the Chemical Society; (1963); p. 2633,2634, View in Reaxys 16 of 17

Solubility [g·l-1]

0.18

Saturation

in pure solvent

Temperature (Solubility (MCS)) [°C]

25

Solvent (Solubility (MCS))

H2O

Andrews; Keefer; Journal of the American Chemical Society; vol. 72; (1950); p. 3113, View in Reaxys 17 of 17

Solubility [g·l-1]

0.347

Saturation

in solution

Temperature (Solubility (MCS)) [°C]

30

Solvent (Solubility (MCS))

H2O

Gross; Saylor; Gorman; Journal of the American Chemical Society; vol. 55; (1933); p. 650, View in Reaxys; van Arkel; Vles; Recueil des Travaux Chimiques des Pays-Bas; vol. 55; (1936); p. 407,408, View in Reaxys Solution Behaviour (MCS) (17) 1 of 17

Description (Solution Behaviour (MCS))

Solubility [Ostwald absorption coefficient]

Solvent (Solution Behaviour (MCS))

aq. NH3

Temperature (Solution Be- 29.85 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

air

Goergenyi, Miklos; Dewulf, Jo; Van Langenhove, Herman; Kiraly, Zoltan; Chemosphere; vol. 59; nb. 8; (2005); p. 1083 1090, View in Reaxys 2 of 17

Description (Solution Behaviour (MCS))

Solubility [Ostwald absorption coefficient]

Solvent (Solution Behaviour (MCS))

H2O

Temperature (Solution Be- 29.85 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

air

Goergenyi, Miklos; Dewulf, Jo; Van Langenhove, Herman; Kiraly, Zoltan; Chemosphere; vol. 59; nb. 8; (2005); p. 1083 1090, View in Reaxys 3 of 17

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

sodium dodecyl-sulfate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 4 of 17

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C]

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Partner (Solution Behaviour (MCS))

sodium cholate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 5 of 17

Description (Solution Behaviour (MCS))

Solubilizing

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

lithium perfluoro-1-octanesufonate

Yang; Khaledi; Analytical chemistry; vol. 67; nb. 3; (1995); p. 499 - 510, View in Reaxys 6 of 17

Description (Solution Behaviour (MCS))

Solubilizing

Solvent (Solution Behaviour (MCS))

H2O

Temperature (Solution Be- 24.9 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

2-{2-[4-(1,1,3,3-tetramethyl-butyl)-phenoxy]-ethoxy}-ethanol

Suslov, D. A.; Solomonov, B. N.; Russian Journal of Physical Chemistry; vol. 69; nb. 7; (1995); p. 1140 - 1143; Zhurnal Fizicheskoi Khimii; vol. 69; nb. 7; (1995); p. 1264 - 1267, View in Reaxys 7 of 17

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

O2

Makitra, R. G.; Pirig, Ya. N.; Politanskaya, T. I.; J. Appl. Chem. USSR (Engl. Transl.); vol. 54; nb. 1; (1981); p. 54 - 58,47 51, View in Reaxys 8 of 17

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

He

Makitra, R. G.; Pirig, Ya. N.; Politanskaya, T. I.; J. Appl. Chem. USSR (Engl. Transl.); vol. 54; nb. 1; (1981); p. 54 - 58,47 51, View in Reaxys 9 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 23; (1973); p. 1,8, View in Reaxys; Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys; Naumenko et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 42; (1969); p. 2522,2376, View in Reaxys 10 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

Partner (Solution Behaviour (MCS))

helium

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 11 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

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Partner (Solution Behaviour (MCS))

neon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 12 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

Partner (Solution Behaviour (MCS))

argon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 13 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Comment (Solution Behaviour (MCS))

sowie bei 25grad, 40grad und 55grad.

Partner (Solution Behaviour (MCS))

krypton

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 14 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 15 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

xenon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 15 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 55 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

xenon

Saylor; Battino; Journal of Physical Chemistry; vol. 62; (1958); p. 1334,1335, View in Reaxys 16 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

water

Wing; Johnston; Journal of the American Chemical Society; vol. 79; (1957); p. 864, View in Reaxys 17 of 17

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- -78.5 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

n-heptane; toluene; hydrogenchloride

Brown; Brady; Journal of the American Chemical Society; vol. 74; (1952); p. 3570,3575, View in Reaxys Sound Properties (7) Description (Sound Comment (Sound Properties) Properties)

References

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102/144

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Sound absorption

Khabibullaev et al.; Moscow University Chemistry Bulletin (English Translation); vol. 27; nb. 3; (1971); p. 66; ; p. 337, View in Reaxys

Ultrasonic properties

Plass; Berichte der Bunsen-Gesellschaft; vol. 74; (1970); p. 343,344-346, View in Reaxys

Velocity of sound

in fluessigem Jodbenzol bei 15grad und 25grad.

Collins; Navidi; Journal of Chemical Physics; vol. 22; (1954); p. 1254, View in Reaxys

Sound absorption

bei Temperaturen von -26grad bis +46grad.

Sette; Ricerca Scientifica; vol. 22; (1952); p. 706,708, View in Reaxys

Velocity of sound

im Bereich von 0grad (1170 m/sec) bis 60grad (1008 m/sec).

Lagemann; McMillan; Woolf; Journal of Chemical Physics; vol. 17; (1949); p. 370, View in Reaxys

Velocity of sound

in Jodbenzol bei 20grad: 1117 m/ sec.

Schaaffs; Zeitschrift fuer Naturforschung; vol. 3a; (1948); p. 396,402, View in Reaxys

Velocity of sound

1114 m/sec.

Lagemann; Evans; McMillan; Journal of the American Chemical Society; vol. 70; (1948); p.

2997, View in Reaxys

Space Group (1) References Henshaw; Acta Crystallographica; vol. 14; (1961); p. 1080, View in Reaxys Static Dielectric Constant (4) Static Dielectric Temperature (Static References Constant Dielectric Constant) [°C] Mallikarjun; Hill; Transactions of the Faraday Society; vol. 61; (1965); p. 1389,1394, View in Reaxys; Hassell; Walker; Transactions of the Faraday Society; vol. 62; (1966); p.

2695,2699, View in Reaxys 4.61

30

Murty; Journal of Scientific and Industrial Research; vol. 18 B; (1959); p. 268,269, View in Reaxys

4.63

20

Timmermans et al.; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p. 5,19, View in Reaxys

3.05 - 4.486

-75 - 20

Philippe; Piette; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p. 600,623, View in Reaxys

Surface Tension (6) Surface Tension Temperature (Sur[g·s-2] face Tension) [°C] 39.57

20

References Korosi; Kovats; Journal of Chemical and Engineering Data; vol. 26; nb. 3; (1981); p. 323 - 332, View in Reaxys Junghaehnel; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 1; (1961); p. 126, View in Reaxys

31.39 - 39.38

18.4 - 90

Vogel; Journal of the Chemical Society; (1948); p. 642; Journal of the Chemical Society; (1934); p. 339, View in Reaxys

38.3

25

Guimaraes de Carvalho; Anais Acad. brasil. Cienc.; vol. 20; (1948); p. 75,82, View in Reaxys

22.64 - 41.21

14 - 180

Sugden; Journal of the Chemical Society; vol. 125; (1924); p. 1173, View in Reaxys

20.7 - 41

-21 - 176

Jaeger; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 101; (1917); p. 155, View in Reaxys; Morgan; Daghlian; Journal of the American Chemical Society; vol. 33; (1911); p. 675; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 173, View in Reaxys; Hardy; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 88; (1913); p. 311; Chem. Zentralbl.; vol.

84; nb. II; (1913); p. 403, View in Reaxys

Transition Point(s) of Liquid Modification(s) (1) Temperature (Tran- Change of Modifi- References sition Point(s) of cation Liquid Modification(s)) [°C]

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-123.4

From crystalline to -

Murthy, S. S. N.; Gangasharan; Nayak, S. K.; Journal of the Chemical Society, Faraday Transactions; vol. 89; nb. 3; (1993); p. 509 - 514, View in Reaxys

Transport Data (1) Description (Trans- References port Data) Thermal conductiv- Filippow; Vestnik Moskovskogo Universiteta; vol. 9; nb. 12; (1954); p. 45; Chem.Abstr.; (1955); p. 15430, ity View in Reaxys; Riedel; Ch. Ing. Tech.; vol. 23; (1951); p. 321,323, View in Reaxys; Riedel; Mitt. Kaeltetechn. Inst.; nb. 2; (1948); p. 3,23, View in Reaxys Transport Phenomena (MCS) (12) 1 of 12

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25

Partner (Transport Phenomena (MCS))

N,N-dimethyl-formamide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 2 of 12

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25

Partner (Transport Phenomena (MCS))

dimethyl sulfoxide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 3 of 12

Description (Transport Phenomena (MCS))

Diffusion

Temperature (Transport Phenomena (MCS)) [°C]

25

Partner (Transport Phenomena (MCS))

acetonitrile

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 4 of 12

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25

Partner (Transport Phenomena (MCS))

acetonitrile

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 5 of 12

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25

Partner (Transport Phenomena (MCS))

dimethyl sulfoxide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys 6 of 12

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

25

Partner (Transport Phenomena (MCS))

N,N-dimethyl-formamide

Casado, J.; Domenech, J.; Gallardo, I.; Monatshefte fuer Chemie; vol. 115; (1984); p. 1143 - 1150, View in Reaxys

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7 of 12

Description (Transport Phenomena (MCS))

Diffusion

Lusis; Ratcliff; AIChE Journal; vol. 17; (1971); p. 1492,1493, View in Reaxys 8 of 12

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

benzene; toluene

Temperature (Transport Phenomena (MCS)) [°C]

7.3

Herzog; Illig; Kudar; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 167; (1934); p. 329,336, View in Reaxys 9 of 12

Description (Transport Phenomena (MCS))

Viscosity

Solvent (Transport Phenomena (MCS))

benzene

Meyer,J.; Mylius; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 95; (1920); p. 356, View in Reaxys 10 of 12

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

methanol

Thovert; Annales de Physique (Paris, France); vol. <9>2; (1914); p. 417; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 150; (1910); p. 270, View in Reaxys 11 of 12

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

benzene

Thovert; Annales de Physique (Paris, France); vol. <9>2; (1914); p. 417; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 150; (1910); p. 270, View in Reaxys 12 of 12

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

ethanol

Oeholm; Chem. Zentralbl.; vol. 84; nb. I; (1913); p. 1650, View in Reaxys Vapour Pressure (15) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

Comment (Vapour Pressure)

References

0.395215

10.64

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

0.478998

13.64

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

0.60261

16.74

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

0.723372

19.84

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

0.771827

20.84

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Bo-

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2018-06-17 20:23:57

ris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys 0.945845

23.64

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

1.11536

26.44

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

1.38989

29.44

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

1.66967

32.54

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

2.0417

35.54

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

2.42949

38.64

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

2.9583

41.44

Liquid

Verevkin, Sergey P.; Sazonova, Aleksandra Yu.; Emel'yanenko, Vladimir N.; Zaitsau, Dzmitry H.; Varfolomeev, Mikhail A.; Solomonov, Boris N.; Zherikova, Kseniya V.; Journal of Chemical and Engineering Data; vol. 60; nb. 1; (2015); p. 89 - 103, View in Reaxys

0.0003 - 0.037

-21.9 - 26.1

Silberman-Granowsskaja; Schugam; Zhurnal Fizicheskoi Khimii; vol. 14; (1940); p. 1004; Chem.Abstr.; (1941); p. 3867, View in Reaxys

0.03 - 0.68

-24.5 - 18.3

Muendel; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 85; (1913); p. 454, View in Reaxys; Drucker; Jimeno; Kangro; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 90; (1915); p. 529, View in Reaxys diagram exists.

Rolla; Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Naturali, Rendiconti; vol. <5> 18 II; (1909); p. 371, View in Reaxys; Feitler; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 4; (1889); p. 72, View in Reaxys; Young; Journal of the Chemical Society; vol. 55; (1889); p. 501; Pr. Roy. Dublin Soc.; vol. 12; (1909); p. 422, View in Reaxys

NMR Spectroscopy (93) 1 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Bergström, Maria; Suresh, Ganji; Naidu, Veluru Ramesh; Unelius, C. Rikard; European Journal of Organic Chemistry; vol.

2017; nb. 22; (2017); p. 3234 - 3239, View in Reaxys 2 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

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Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Bergström, Maria; Suresh, Ganji; Naidu, Veluru Ramesh; Unelius, C. Rikard; European Journal of Organic Chemistry; vol.

2017; nb. 22; (2017); p. 3234 - 3239, View in Reaxys 3 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Liu, Wenbo; Yang, Xiaobo; Gao, Yang; Li, Chao-Jun; Journal of the American Chemical Society; vol. 139; nb. 25; (2017); p.

8621 - 8627, View in Reaxys 4 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 125 scopy) [MHz] Location

supporting information

Liu, Wenbo; Yang, Xiaobo; Gao, Yang; Li, Chao-Jun; Journal of the American Chemical Society; vol. 139; nb. 25; (2017); p.

8621 - 8627, View in Reaxys 5 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Temperature (NMR Spectroscopy) [°C]

24.84

Location

supporting information

Stridfeldt, Elin; Lindstedt, Erik; Reitti, Marcus; Blid, Jan; Norrby, Per-Ola; Olofsson, Berit; Chemistry - A European Journal; vol. 23; nb. 53; (2017); p. 13249 - 13258, View in Reaxys 6 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

[D3]acetonitrile

Achar, Tapas Kumar; Maiti, Saikat; Mal, Prasenjit; Organic and Biomolecular Chemistry; vol. 14; nb. 20; (2016); p. 4654 4663, View in Reaxys 7 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

tetrahydrofuran-d8

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Location

supporting information

Martinez, Gabriel Espinosa; Ocampo, Cristian; Park, Yun Ji; Fout, Alison R.; Journal of the American Chemical Society; vol. 138; nb. 13; (2016); p. 4290 - 4293, View in Reaxys 8 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

benzene-d6

Location

supporting information

Losch; Kolb; Astafan; Daou; Pinard; Pale; Louis; Green Chemistry; vol. 18; nb. 17; (2016); p. 4714 - 4724, View in Reaxys 9 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

benzene-d6

Location

supporting information

Losch; Kolb; Astafan; Daou; Pinard; Pale; Louis; Green Chemistry; vol. 18; nb. 17; (2016); p. 4714 - 4724, View in Reaxys 10 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Luquin, Asunción; Castillo, Noelia; Cerrada, Elena; Merchan, Francisco L.; Garrido, Julian; Laguna, Mariano; European Journal of Organic Chemistry; vol. 2016; nb. 4; (2016); p. 789 - 798, View in Reaxys 11 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Location

supporting information

De Haro, Teresa; Nevado, Cristina; Journal of the American Chemical Society; vol. 132; nb. 5; (2010); p. 1512 - 1513, View in Reaxys; Yang, Hengquan; Fu, Luman; Wei, Lijuan; Liang, Jifen; Binks, Bernard P.; Journal of the American Chemical Society; vol. 137; nb. 3; (2015); p. 1362 - 1371, View in Reaxys 12 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Suzuki, Yuhsuke; Ishiwata, Yoshihide; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron Letters; vol. 51; nb. 45; (2010); p.

5950 - 5953, View in Reaxys; Naoe, Kazumitsu; Ando, Tatsuya; Kawasaki, Kenta; Imai, Masanao; Chemical Papers; vol.

70; nb. 2; (2015); p. 164 - 171, View in Reaxys 13 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

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Solvents (NMR Spectroscopy)

tetradeuterioacetic acid

Location

supporting information

Cook, Amanda K.; Sanford, Melanie S.; Journal of the American Chemical Society; vol. 137; nb. 8; (2015); p. 3109 - 3118, View in Reaxys 14 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

[D3]acetonitrile

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Kaszyński, Piotr; Ringstrand, Bryan; Angewandte Chemie - International Edition; vol. 54; nb. 22; (2015); p. 6576 - 6581; Angew. Chem.; vol. 127; nb. 22; (2015); p. 6676 - 6681,6, View in Reaxys 15 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

[D3]acetonitrile

Frequency (NMR Spectro- 500 scopy) [MHz] Tokarz, Paweł; Kaszyński, Piotr; Domagała, Sławomir; Woźniak, Krzysztof; Journal of Organometallic Chemistry; vol.

798; (2015); p. 70 - 79, View in Reaxys 16 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 300 scopy) [MHz] Location

supporting information

Niu, Liting; Zhang, Hao; Yang, Haijun; Fu, Hua; Synlett; vol. 25; nb. 7; (2014); p. 995 - 1000; Art.No: 691, View in Reaxys 17 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 75 scopy) [MHz] Location

supporting information

Niu, Liting; Zhang, Hao; Yang, Haijun; Fu, Hua; Synlett; vol. 25; nb. 7; (2014); p. 995 - 1000; Art.No: 691, View in Reaxys 18 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Location

supporting information

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109/144

2018-06-17 20:23:57

Bhattacharya, Moumita; Cluff, David B.; Das, Siddhartha; Inorganica Chimica Acta; vol. 423; nb. PA; (2014); p. 238 - 241, View in Reaxys 19 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Williams, Thomas J.; Fairlamb, Ian J.S.; Tetrahedron Letters; vol. 54; nb. 23; (2013); p. 2906 - 2908, View in Reaxys 20 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

26.84

Location

supporting information

Baralle, Alexandre; Fensterbank, Louis; Goddard, Jean-Philippe; Ollivier, Cyril; Chemistry - A European Journal; vol. 19; nb. 33; (2013); p. 10809 - 10813, View in Reaxys 21 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

[D3]acetonitrile

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Kiyokawa, Kensuke; Kosaka, Tomoki; Minakata, Satoshi; Organic Letters; vol. 15; nb. 18; (2013); p. 4858 - 4861, View in Reaxys 22 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

[D3]acetonitrile

Frequency (NMR Spectro- 100 scopy) [MHz] Location

supporting information

Kiyokawa, Kensuke; Kosaka, Tomoki; Minakata, Satoshi; Organic Letters; vol. 15; nb. 18; (2013); p. 4858 - 4861, View in Reaxys 23 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

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Temperature (NMR Spectroscopy) [°C]

19.84

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Huang, Chang-Cang; Liu, Jian-Jun; Chen, Yong; Lin, Mei-Jin; Chemical Communications; vol. 49; nb. 98; (2013); p. 11512 - 11514, View in Reaxys 24 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Location

supporting information

Wang, Liqiang; Lu, Wenjun; Organic Letters; vol. 11; nb. 5; (2009); p. 1079 - 1082, View in Reaxys; Seo, Sangwon; Taylor, John B.; Greaney, Michael F.; Chemical Communications; vol. 48; nb. 66; (2012); p. 8270 - 8272, View in Reaxys 25 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Zhang, Peng; Sun, Dongqing; Wen, Mingwei; Yang, Jingkui; Zhou, Kebin; Wang, Zhixiang; Advanced Synthesis and Catalysis; vol. 354; nb. 4; (2012); p. 720 - 729, View in Reaxys 26 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Zhang, Peng; Sun, Dongqing; Wen, Mingwei; Yang, Jingkui; Zhou, Kebin; Wang, Zhixiang; Advanced Synthesis and Catalysis; vol. 354; nb. 4; (2012); p. 720 - 729, View in Reaxys 27 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Song, Hyon Min; Moosa, Basem A.; Khashab, Niveen M.; Journal of Materials Chemistry; vol. 22; nb. 31; (2012); p. 15953 15959, View in Reaxys

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28 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Zayas, Hazit A.; Valade, David; Jia, Zhongfan; Monteiro, Michael J.; Australian Journal of Chemistry; vol. 65; nb. 8; (2012); p. 1090 - 1094, View in Reaxys 29 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 600 scopy) [MHz] Location

supporting information

Yang, Haijun; Li, Yong; Jiang, Min; Wang, Junmei; Fu, Hua; Chemistry - A European Journal; vol. 17; nb. 20; (2011); p.

5652 - 5660, View in Reaxys 30 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 150 scopy) [MHz] Location

supporting information

Yang, Haijun; Li, Yong; Jiang, Min; Wang, Junmei; Fu, Hua; Chemistry - A European Journal; vol. 17; nb. 20; (2011); p.

5652 - 5660, View in Reaxys 31 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Location

supporting information

Ton, Thi My Uyen; Tejo, Ciputra; Tania, Stefani; Chang, Joyce Wei Wei; Chan, Philip Wai Hong; Journal of Organic Chemistry; vol. 76; nb. 12; (2011); p. 4894 - 4904, View in Reaxys 32 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Frequency (NMR Spectro- 400 scopy) [MHz] Ochiai, Bungo; Shimada, Yohei; Reactive and Functional Polymers; vol. 71; nb. 8; (2011); p. 791 - 795, View in Reaxys 33 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

19.84

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Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Albert, Brian J.; Yamamoto, Hisashi; Angewandte Chemie - International Edition; vol. 49; nb. 15; (2010); p. 2747 - 2749, View in Reaxys 34 of 93

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Temperature (NMR Spectroscopy) [°C]

19.84

Frequency (NMR Spectro- 126 scopy) [MHz] Location

supporting information

Albert, Brian J.; Yamamoto, Hisashi; Angewandte Chemie - International Edition; vol. 49; nb. 15; (2010); p. 2747 - 2749, View in Reaxys 35 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 100 scopy) [MHz] Suzuki, Yuhsuke; Ishiwata, Yoshihide; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron Letters; vol. 51; nb. 45; (2010); p.

5950 - 5953, View in Reaxys 36 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

dichloromethane-d2

Frequency (NMR Spectro- 250 scopy) [MHz] Hashmi, A. Stephen K.; Ramamurthi, Tanuja Dondeti; Todd, Matthew H.; Tsang, Althea S.-K.; Graf, Katharina; Australian Journal of Chemistry; vol. 63; nb. 12; (2010); p. 1619 - 1626, View in Reaxys 37 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 250 scopy) [MHz] Zarei, Amin; Hajipour, Abdol R.; Khazdoozd, Leila; Synthesis; nb. 6; (2009); p. 941 - 944; Art.No: Z19108SS, View in Reaxys 38 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

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113/144

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Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 500 scopy) [MHz] Comment (NMR Spectroscopy)

in the presence of organic compounds

Hubbard, Abigail; Okazaki, Takao; Laali, Kenneth K.; Journal of Organic Chemistry; vol. 73; nb. 1; (2008); p. 316 - 319, View in Reaxys 39 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 125 scopy) [MHz] Comment (NMR Spectroscopy)

in the presence of organic compounds

Hubbard, Abigail; Okazaki, Takao; Laali, Kenneth K.; Journal of Organic Chemistry; vol. 73; nb. 1; (2008); p. 316 - 319, View in Reaxys 40 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 300 scopy) [MHz] Hossain, Md. Delwar; Oyamada, Juzo; Kitamura, Tsugio; Synthesis; nb. 5; (2008); p. 690 - 692, View in Reaxys 41 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 75 scopy) [MHz] Hossain, Md. Delwar; Oyamada, Juzo; Kitamura, Tsugio; Synthesis; nb. 5; (2008); p. 690 - 692, View in Reaxys 42 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400 scopy) [MHz] Hagio, Hiroyuki; Sugiura, Masaharu; Kobayashi, Shu; Organic Letters; vol. 8; nb. 3; (2006); p. 375 - 378, View in Reaxys 43 of 93

Nucleus (NMR Spectroscopy)

1H

Coupling Nuclei

1H

Solvents (NMR Spectroscopy)

CDCl3

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Frequency (NMR Spectro- 400 scopy) [MHz] Hagio, Hiroyuki; Sugiura, Masaharu; Kobayashi, Shu; Organic Letters; vol. 8; nb. 3; (2006); p. 375 - 378, View in Reaxys 44 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 100 scopy) [MHz] Hagio, Hiroyuki; Sugiura, Masaharu; Kobayashi, Shu; Organic Letters; vol. 8; nb. 3; (2006); p. 375 - 378, View in Reaxys 45 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Frequency (NMR Spectro- 400.13 scopy) [MHz] Abraham, Raymond J.; Byrne, Jonathan J.; Griffiths, Lee; Perez, Manuel; Magnetic Resonance in Chemistry; vol. 44; nb.

5; (2006); p. 491 - 509, View in Reaxys 46 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Frequency (NMR Spectro- 400.13 scopy) [MHz] Abraham, Raymond J.; Byrne, Jonathan J.; Griffiths, Lee; Perez, Manuel; Magnetic Resonance in Chemistry; vol. 44; nb.

5; (2006); p. 491 - 509, View in Reaxys 47 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Evans, P. Andrew; Brandt, Thomas A.; Journal of Organic Chemistry; vol. 62; nb. 16; (1997); p. 5321 - 5326, View in Reaxys; Ozanne-Beaudenon, Aurelie; Quideau, Stephane; Angewandte Chemie - International Edition; vol. 44; nb.

43; (2005); p. 7065 - 7069, View in Reaxys 48 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Smith,William B.; Ho, Oliver Chenpu; Journal of Organic Chemistry; vol. 55; nb. 8; (1990); p. 2543 - 2545, View in Reaxys; Wilson, Stephen R.; Jacob, Linda A.; Journal of Organic Chemistry; vol. 51; nb. 25; (1986); p. 4833 - 4836, View in Reaxys; Cerfontain; Zou; Bakker; van de Griendt; Canadian Journal of Chemistry; vol. 72; nb. 9; (1994); p. 1966 - 1971, View in Reaxys; Menger, Fredric M.; Sanchez, Ana M.; Chemical Communications; nb. 2; (1997); p. 199 - 200, View in Reaxys; Makowiec, Slawomir; Rachon, Janusz; Phosphorus, Sulfur and Silicon and Related Elements; vol. 177; nb. 4; (2002); p. 941 - 955, View in Reaxys 49 of 93

Description (NMR Spectroscopy)

Chemical shifts

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115/144

2018-06-17 20:23:57

Nucleus (NMR Spectroscopy)

13C

Reetz, Manfred T.; Westermann, Elke; Angewandte Chemie - International Edition; vol. 39; nb. 1; (2000); p. 165 - 168, View in Reaxys 50 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

H2O; 2-methyl-propan-2-ol

Frequency (NMR Spectro- 400 scopy) [MHz] Bunton, Clifford A.; Foroudian, Houshang J.; Gillitt, Nicholas D.; Journal of Physical Organic Chemistry; vol. 12; nb. 10; (1999); p. 758 - 764, View in Reaxys 51 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

acetone-d6

Brazdil, Linda C.; Fitch, Jill L.; Cutler, Carlo J.; Haynik, Denise M.; Ace, Eryn R.; Journal of the Chemical Society. Perkin Transactions 2; nb. 4; (1998); p. 933 - 936, View in Reaxys 52 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

various solvent(s)

Menger, Fredric M.; Sanchez, Ana M.; Chemical Communications; nb. 2; (1997); p. 199 - 200, View in Reaxys 53 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

-10

Carey, Joseph V.; Chaloner, Penny A.; Seddon, Kenneth R.; Taylor, Michael; Journal of Chemical Research - Part S; nb. 3; (1996); p. 156 - 157, View in Reaxys 54 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Smith,William B.; Ho, Oliver Chenpu; Journal of Organic Chemistry; vol. 55; nb. 8; (1990); p. 2543 - 2545, View in Reaxys; Brace, Neal O.; Marshall, Lawrence W.; Pinson, Carol J.; Wingerden, Gail van; Journal of Organic Chemistry; vol. 49; nb.

13; (1984); p. 2361 - 2368, View in Reaxys; Katritzky, Alan R.; Gallos, John K.; Durst, H. Dupont; Magnetic Resonance in Chemistry; vol. 27; nb. 9; (1989); p. 815 - 822, View in Reaxys; Cook, Iain B.; Australian Journal of Chemistry; vol. 42; nb. 9; (1989); p. 1493 - 1518, View in Reaxys; Kabilan, S.; Ganapathi, A.; Sankar, P.; Krishnasamy, K.; Journal of Chemical Research, Synopses; nb. 7; (1995); p. 280 - 281, View in Reaxys 55 of 93

Description (NMR Spectroscopy)

Chemical shifts

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

116/144

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Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

25

Robbins, Timothy A.; Knobler, Carolyn B.; Bellew, Donald R.; Cram, Donald J.; Journal of the American Chemical Society; vol. 116; nb. 1; (1994); p. 111 - 122, View in Reaxys 56 of 93

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Comment (NMR Spectroscopy)

1H-1H

Smith,William B.; Ho, Oliver Chenpu; Journal of Organic Chemistry; vol. 55; nb. 8; (1990); p. 2543 - 2545, View in Reaxys; Wilson, Stephen R.; Jacob, Linda A.; Journal of Organic Chemistry; vol. 51; nb. 25; (1986); p. 4833 - 4836, View in Reaxys; Cerfontain; Zou; Bakker; van de Griendt; Canadian Journal of Chemistry; vol. 72; nb. 9; (1994); p. 1966 - 1971, View in Reaxys 57 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

tetrahydrofuran

Temperature (NMR Spectroscopy) [°C]

-105

Reich, Hans J.; Green, D. Patric; Phillips, Nancy H.; Journal of the American Chemical Society; vol. 113; nb. 4; (1991); p.

1414 - 1416, View in Reaxys; Reich, Hans J.; Green, D. Patrick; Phillips, Nancy H.; Journal of the American Chemical Society; vol. 111; nb. 9; (1989); p. 3444 - 3445, View in Reaxys 58 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

nematic phase

Ugolini, R.; Diehl, P.; Journal of Molecular Structure; vol. 216; (1990); p. 325 - 332, View in Reaxys 59 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

various solvent(s)

Kowalewski, D. G. De; Santos, C. De Los; Journal of Molecular Structure; vol. 221; (1990); p. 299 - 308, View in Reaxys 60 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CCl4

Temperature (NMR Spectroscopy) [°C]

27 - 30

Biekofsky, Rodolfo R.; Pomilio, Alicia B.; Contreras, Ruben H.; Kowalewski, Dora G. de; Facelli, Julio C.; Magnetic Resonance in Chemistry; vol. 27; nb. 2; (1989); p. 158 - 161, View in Reaxys

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2018-06-17 20:23:57

61 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Temperature (NMR Spectroscopy) [°C]

30

Faure, Robert; Llinares, Jeanine; Elguero, Jose; Goya, Pilar; Bulletin des Societes Chimiques Belges; vol. 96; nb. 8; (1987); p. 603 - 618, View in Reaxys 62 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

nitromethane

Contreras, R. H.; Ferraro, M. B.; Kowalewski, D. G. de; Diaz, L.; Magnetic Resonance in Chemistry; vol. 23; nb. 5; (1985); p. 296 - 300, View in Reaxys 63 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CH2Cl2

Temperature (NMR Spectroscopy) [°C]

35

Guillaume, F.; Seguin, J. P.; Nadjo, L.; Uzan, R.; Membrey, F.; Doucet, J.P.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); nb. 7; (1984); p. 1139 - 1144, View in Reaxys 64 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

dimethylsulfoxide-d6

Temperature (NMR Spectroscopy) [°C]

26.9

O'Connor, Charmian J.; McLennan, Duncan J.; Calvert, David J.; Lomax, Terence D.; Porter, Anthony J.; Rogers, David A.; Australian Journal of Chemistry; vol. 37; nb. 3; (1984); p. 497 - 510, View in Reaxys 65 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

24.9

Fung; Kong; Journal of the American Chemical Society; vol. 106; nb. 21; (1984); p. 6193 - 6196, View in Reaxys 66 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Temperature (NMR Spectroscopy) [°C]

-60 - 10

Smegal, John A.; Schardt, Bruce C.; Hill, Craig L.; Journal of the American Chemical Society; vol. 105; nb. 11; (1983); p.

3510 - 3515, View in Reaxys 67 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

30

Bailey, William F.; Cioffi, Eugene A.; Wiberg, Kenneth B.; Journal of Organic Chemistry; vol. 46; nb. 21; (1981); p. 4219 4225, View in Reaxys 68 of 93

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

acetone-d6

Comment (NMR Spectroscopy)

13C-13C.

Wray, V.; Ernst, L.; Lund, T.; Jakobsen, H. J.; Journal of Magnetic Resonance (1969-1992); vol. 40; nb. 1; (1980); p. 55 - 68, View in Reaxys 69 of 93

Description (NMR Spectroscopy)

NMR

Llabres,G. et al.; Canadian Journal of Chemistry; vol. 56; (1978); p. 2008 - 2012, View in Reaxys; Friedrich,K. et al.; Chemische Berichte; vol. 111; (1978); p. 2099 - 2107, View in Reaxys; Balthazor,T.M. et al.; Journal of Organic Chemistry; vol. 44; (1979); p. 1447 - 1449, View in Reaxys; Tarpley,A.R.; Goldstein,J.H.; Journal of Physical Chemistry; vol. 76; (1972); p. 515, View in Reaxys; Syrova; Sheinker; Chemistry of Heterocyclic Compounds (New York, NY, United States); vol. 8; (1972); p.

313; Khimiya Geterotsiklicheskikh Soedinenii; vol. 8; (1972); p. 345, View in Reaxys; Freymann et al.; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 3; (1962); p. 1222, View in Reaxys; Hruska et al.; Canadian Journal of Chemistry; vol. 43; (1965); p.

2392,2393, View in Reaxys; Heimanek et al.; Journal of the Chemical Society, Chemical Communications; (1977); p. 561, View in Reaxys; Miyajima et al.; Chemical and Pharmaceutical Bulletin; vol. 19; (1971); p. 2301,2305, View in Reaxys; Norton; Tetrahedron; vol. 33; (1977); p. 2577,2579, 2580, View in Reaxys; Olah et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 680, View in Reaxys; Shkurko; Zhurnal Organicheskoi Khimii; vol. 13; (1977); p. 918,842,844, View in Reaxys; Inamoto; Masuda; Tetrahedron Letters; (1977); p. 3287, View in Reaxys; Glukhikh; Voronkov; Doklady Physical Chemistry; vol. 244-249; (1979); p. 744, View in Reaxys; Coulson; Journal of the American Chemical Society; vol. 98; (1976); p. 3111,3112, View in Reaxys; Spiesecke; Schneider; Journal of Chemical Physics; vol. 35; (1961); p. 731,732,733, View in Reaxys; Lynch; Canadian Journal of Chemistry; vol. 55; (1977); p. 541,543, View in Reaxys; Freymann; Archives des Sciences; vol. 12; (1959); Chem.Abstr.; nb. 11705; (1960), View in Reaxys; Nogina; Koptyug; Zhurnal Organicheskoi Khimii; vol. 8; (1972); p. 1495,1524, View in Reaxys; Lauterbur; Journal of Chemical Physics; vol. 38; (1963); p. 1432,1433,1435, View in Reaxys; Bunce; Murray; Tetrahedron; vol. 27; (1971); p. 5323,5332, View in Reaxys; Read et al.; Tetrahedron Letters; (1968); p. 1215, View in Reaxys; Castellano et al.; Tetrahedron Letters; (1967); p. 4635, View in Reaxys 70 of 93

Description (NMR Spectroscopy)

Spin-spin coupling constants

Weigert; Roberts; Journal of the American Chemical Society; vol. 94; (1972); p. 6021, View in Reaxys; Page; Molecular Physics; vol. 13; (1967); p. 523, View in Reaxys; Tarpley Jr.; Goldstein; Journal of Physical Chemistry; vol. 75; (1971); p. 421,425, View in Reaxys; Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys; Womble; Savitsky; Journal of Magnetic Resonance (1969-1992); vol. 4; (1971); p. 226, View in Reaxys; Read; Goldstein; Journal of Molecular Spectroscopy; vol. 23; (1967); p. 179,181,186, View in Reaxys; Ernst et al.; Journal of Magnetic Resonance (1969-1992); vol. 25; (1977); p. 123,126,128, View in Reaxys 71 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C

bei Zusatz von Di-tert.-butylnitroxid-Radikal

Morishima et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 4812,4814, View in Reaxys 72 of 93

Description (NMR Spectroscopy)

Chemical shifts

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Comment (NMR Spectroscopy)

13C-Kontakt-Shift m. Di-t-butyl-nitroxid

Morishima et al.; Chemical Physics Letters; vol. 14; (1972); p. 372, View in Reaxys 73 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C-NMR chem. shifts

Smith; Deavenport; Journal of Magnetic Resonance (1969-1992); vol. 7; (1972); p. 364, View in Reaxys 74 of 93

Description (NMR Spectroscopy)

CIDNP

Cooper et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 552, View in Reaxys 75 of 93

Description (NMR Spectroscopy)

NMR in liquid-crystal phase

Haloui; Canet; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 275; (1972); p.

447, View in Reaxys 76 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

1H

Tarpley Jr.; Goldstein; Journal of Physical Chemistry; vol. 75; (1971); p. 421,425, View in Reaxys 77 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Aromatic Solvent Induced Shifts (sF partially deuterated)

Robinson et al.; Journal of Magnetic Resonance (1969-1992); vol. 5; (1971); p. 328, View in Reaxys 78 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Lsgsm. - Einfluss auf intern. Shift

Robinson; Savitzky; Journal of Magnetic Resonance (1969-1992); vol. 2; (1970); p. 269, View in Reaxys 79 of 93

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

NMR-Sp. im Gem. m. Ethyl-Li

Ward et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 746, View in Reaxys 80 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Protonchem. Verschieb.

Nomura et al.; Tetrahedron Letters; (1969); p. 639, View in Reaxys 81 of 93

Description (NMR Spectroscopy)

Chemical shifts

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 28; (1968); p. 89,97, View in Reaxys 82 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

NMR-Abs.

Hayamizu; Yamamoto; Journal of Molecular Spectroscopy; vol. 25; (1968); p. 422,428, View in Reaxys; Read; Goldstein; Journal of Molecular Spectroscopy; vol. 23; (1967); p. 179,181,186, View in Reaxys 83 of 93

Description (NMR Spectroscopy)

Chemical shifts

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2018-06-17 20:23:57

Comment (NMR Spectroscopy)

Lsgm.-Verschieb. durch Stosskomplexbldg. m. Lsgm.

Ledaal; Tetrahedron Letters; (1968); p. 1683, View in Reaxys 84 of 93

Description (NMR Spectroscopy)

Spectrum

Petrosjan; Reutow; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1967); p. 1311; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1967); p. 1361, View in Reaxys 85 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Beziehung zwischen NMR-Verschiebungen u. ν-Elektronendichte

Kanekar et al.; Proceedings - Indian Academy of Sciences, Section A; vol. 65; (1967); p. 353,356, View in Reaxys 86 of 93

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

CCl4

Goetz et al.; Justus Liebigs Annalen der Chemie; vol. 681; (1965); p. 1,2,8, View in Reaxys 87 of 93

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

13C

Lauterbur; Journal of Chemical Physics; vol. 38; (1963); p. 1432,1433,1435, View in Reaxys 88 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

ortho- u. meta-Wasserstoff

Schaefer et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 2969,2971, View in Reaxys 89 of 93

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C

Schaefer et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 2969,2971, View in Reaxys 90 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

benzene

Charton-Koechlin; Leroy; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 56; (1959); p. 850,852, View in Reaxys 91 of 93

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

cyclohexane

Corio; Dailey; Journal of the American Chemical Society; vol. 78; (1956); p. 3043,3045, View in Reaxys 92 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

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Solvents (NMR Spectroscopy)

CCl4

Bothner-By; Glick; Journal of the American Chemical Society; vol. 78; (1956); p. 1071; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1654, View in Reaxys 93 of 93

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

iodobenzene

Bothner-By; Glick; Journal of the American Chemical Society; vol. 78; (1956); p. 1071; Journal of Chemical Physics; vol. 26; (1957); p. 1651,1654, View in Reaxys IR Spectroscopy (37) 1 of 37

Description (IR Spectroscopy)

ATR (attenuated total reflectance); Bands; Spectrum

Location

supporting information

Inkpen, Michael S.; Du, Shuoren; Hildebrand, Mariana; White, Andrew J. P.; Harrison, Nicholas M.; Albrecht, Tim; Long, Nicholas J.; Organometallics; vol. 34; nb. 22; (2015); p. 5461 - 5469, View in Reaxys 2 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

chloroform-d1

Temperature (IR Spectroscopy) [°C]

-60

Location

supporting information

Banert, Klaus; Hagedorn, Manfred; Wu, Zhuang; Zeng, Xiaoqing; McPhee, Derek J.; Molecules; vol. 20; nb. 12; (2015); p. 21328 - 21335, View in Reaxys 3 of 37

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

neat liquid

Suzuki, Yuhsuke; Ishiwata, Yoshihide; Moriyama, Katsuhiko; Togo, Hideo; Tetrahedron Letters; vol. 51; nb. 45; (2010); p.

5950 - 5953, View in Reaxys 4 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

potassium bromide

Zarei, Amin; Hajipour, Abdol R.; Khazdoozd, Leila; Synthesis; nb. 6; (2009); p. 941 - 944; Art.No: Z19108SS, View in Reaxys 5 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

neat liquid

Temperature (IR Spectroscopy) [°C]

25

Keefe, C. Dale; Butler, Ellen; Gillis, Elizabeth; MacDonald, Jennifer L.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 1; (2007); p. 125 - 138, View in Reaxys 6 of 37

Description (IR Spectroscopy)

Intensity of IR bands

Brownlee et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 557,559, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Schmid; Bellanato; Zeitschrift fuer Elektrochemie; vol. 65; (1961); p. 362, View in Reaxys; Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Cameron et al.; Journal of Chemical Physics; vol. 56; (1972); p.

4717, View in Reaxys; Koeser, Heinz J. K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 2; (1984); p. 125 - 136, View in Reaxys; Keefe, C. Dale; Butler, Ellen; Gillis, Elizabeth; MacDonald, Jennifer L.; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 67; nb. 1; (2007); p. 125 - 138, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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7 of 37

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

24.94

Jagiella, Stefan; Zabel, Friedhelm; Physical Chemistry Chemical Physics; vol. 9; nb. 36; (2007); p. 5036 - 5051, View in Reaxys 8 of 37

Description (IR Spectroscopy)

Bands

Temperature (IR Spectroscopy) [°C]

24.94

Jagiella, Stefan; Zabel, Friedhelm; Physical Chemistry Chemical Physics; vol. 9; nb. 36; (2007); p. 5036 - 5051, View in Reaxys 9 of 37

Description (IR Spectroscopy)

Spectrum

Krueger; Mettee; Canadian Journal of Chemistry; vol. 42; (1964); p. 288,289, View in Reaxys; Freymann et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 265; (1967); p. 771, View in Reaxys; Korostelev et al.; Journal of Applied Spectroscopy; vol. 27; (1977); p. 1487, View in Reaxys; Lisitsa; Journal of Applied Spectroscopy; vol. 27; nb. 4; (1977); p. 1243 - 1250, View in Reaxys; Griffiths; Thompson; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 298; (1967); p. 51,54, View in Reaxys; Nesmejanow et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1964); p. 574,576; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1964); p. 613, View in Reaxys; Lebas; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 59; (1962); p. 1072,1073, View in Reaxys; Harrah et al.; Spectrochimica Acta; vol. 18; (1962); p. 21,29, View in Reaxys; Fleming et al.; Molecular Physics; vol. 19; (1970); p. 853,856, View in Reaxys; Langenbucher et al.; Justus Liebigs Annalen der Chemie; vol. 669; (1963); p. 11,13, 20, View in Reaxys; Winkler, Michael; Sander, Wolfram; Journal of Organic Chemistry; vol. 71; nb. 17; (2006); p. 6357 - 6367, View in Reaxys 10 of 37

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

film

Narayanan, Radha; El-Sayed, Mostafa A.; Journal of Physical Chemistry B; vol. 109; nb. 10; (2005); p. 4357 - 4360, View in Reaxys 11 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

film

Narayanan, Radha; El-Sayed, Mostafa A.; Journal of Physical Chemistry B; vol. 109; nb. 10; (2005); p. 4357 - 4360, View in Reaxys 12 of 37

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

20

Comment (IR Spectroscopy)

1540 - 620 cm**(-1)

Koeser, Heinz J. K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 2; (1984); p. 125 136, View in Reaxys 13 of 37

Description (IR Spectroscopy)

Spectrum

Temperature (IR Spectroscopy) [°C]

20

Comment (IR Spectroscopy)

1500 - 600 cm**(-1)

Koeser, Heinz J.K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 6; (1984); p. 547 562, View in Reaxys 14 of 37

Description (IR Spectroscopy)

Spectrum

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2018-06-17 20:23:57

Temperature (IR Spectroscopy) [°C]

15

Comment (IR Spectroscopy)

1500 - 600 cm**(-1)

Koeser, Heinz J.K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 6; (1984); p. 547 562, View in Reaxys 15 of 37

Description (IR Spectroscopy)

Reflection spectrum

Koeser, Heinz J. K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb. 2; (1984); p. 125 136, View in Reaxys; Koeser, Heinz J.K.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 40; nb.

6; (1984); p. 547 - 562, View in Reaxys 16 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

8771 cm**(-1)

Gough, Kathleen M.; Henry, Bryan R.; Journal of Physical Chemistry; vol. 87; nb. 18; (1983); p. 3433 - 3441, View in Reaxys 17 of 37

Description (IR Spectroscopy)

Fine structure of IR bands

Davies et al.; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 73; (1977); p.

1071,1074, View in Reaxys 18 of 37

Description (IR Spectroscopy)

IR

Brownlee,R.T.C. et al.; Journal of the American Chemical Society; vol. 90; nb. 7; (1968); p. 1757 - 1767, View in Reaxys; Bell,R.; Morgan,K.J.; Journal of the Chemical Society; (1960); p. 1209 - 1214, View in Reaxys; Freymann et al.; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 3; (1962); p. 1222, View in Reaxys; McDevitt; Fateley; Journal of Molecular Structure; vol. 5; (1970); p. 477,484, View in Reaxys; Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Wright; Nature; vol. 209; nb. 5023; (1966); p. 571 - 572, View in Reaxys; Vincent-Geisse; Lecomte; Adv. Mol. Spectrosc., Proc. Int. Meet., 4th; vol. 1; (1962); p. 104,107, View in Reaxys; Jain; Walker; Journal of Physical Chemistry; vol. 75; (1971); p. 2942, View in Reaxys; Hindle et al.; Journal of Chemical Physics; vol. 62; (1975); p. 3230, View in Reaxys; Moharram; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 248; (1971); p. 137,140,141, View in Reaxys; Moharram; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 251; (1972); p. 33,35,38, View in Reaxys; Beg; Abbasi; Pakistan Journal of Scientific and Industrial Research; vol. 12; (1969); p. 12, View in Reaxys; Sirkar et al.; Indian Journal of Physics (1926-1976); vol. 38; (1964); p. 610,620, View in Reaxys; Hikal et al.; Spectroscopy Letters; vol. 2; (1969); p. 13,15, View in Reaxys; Horak; Vitek; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1107,1109-1116, View in Reaxys; Kondilenko et al.; Optics and Spectroscopy; vol. 32; (1972); p.

280; ; p. 535, View in Reaxys; Delorme et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol.

261; (1965); p. 3331, View in Reaxys; Delorme; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol.

256; (1963); p. 3272, View in Reaxys; McWhinnie; Poller; Spectrochimica Acta; vol. 22; (1966); p. 501,503, View in Reaxys; Benson et al.; Canadian Journal of Chemistry; vol. 50; (1972); p. 2610, View in Reaxys; Khalimonova; Optics and Spectroscopy; vol. 13; (1962); p. 447; ; p. 791, View in Reaxys; Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys 19 of 37

Description (IR Spectroscopy)

Bands

Lafaix; Vincent-Geisse; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 29; (1973); p. 177, View in Reaxys; Brown et al.; Spectrochimica Acta; vol. 21; (1965); p. 659, View in Reaxys; Freymann et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 265; (1967); p. 771, View in Reaxys 20 of 37

Description (IR Spectroscopy)

Fermi resonance

Lisitsa et al.; Sov. Phys. Dokl. (Engl. Transl.); vol. 7; (1963); p. 1262,748, View in Reaxys 21 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

5000 - 263 cm**(-1)

Plyler; Allen; Tidwell; Journal of Research of the National Bureau of Standards (United States); vol. 58; (1957); p. 255,256, 260, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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22 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1786 - 625 cm**(-1)

Furlani; Sartori; Annali di Chimica (Rome, Italy); vol. 47; (1957); p. 124,126, 133, View in Reaxys 23 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CCl4

Comment (IR Spectroscopy)

3333 - 667 cm**(-1)

Josien; Lebas; Bulletin de la Societe Chimique de France; (1956); p. 53, View in Reaxys 24 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CS2

Comment (IR Spectroscopy)

909 - 667 cm**(-1)

Kross et al.; Journal of the American Chemical Society; vol. 78; (1956); p. 1332, View in Reaxys; Bell; Thompson; Vago; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 192; (1948); p.

498,505, View in Reaxys; Brackett; Liddel; Physical Review; vol. <2> 37; (1931); p. 108, View in Reaxys; Roberts et al.; Journal of the American Chemical Society; vol. 76; (1954); p. 4525,4533, View in Reaxys; Lecomte; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 201; (1935); p. 1340; Journal de Physique et le Radium; vol. <7> 9; (1938); p. 13,22, 24, View in Reaxys; Plyler; Journal of Chemical Physics; vol. 17; (1949); p. 218; Discussions of the Faraday Society; vol. 9; (1950); p. 100, View in Reaxys 25 of 37

Description (IR Spectroscopy)

Intensity of IR bands

Comment (IR Spectroscopy)

bei 1015 cmE-1 und 1600 cmE-1.

Randle; Whiffen; Transactions of the Faraday Society; vol. 52; (1956); p. 9,10, View in Reaxys 26 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

714 - 263 cm**(-1)

Plyler; Discussions of the Faraday Society; vol. 9; (1950); p. 100,102, View in Reaxys 27 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

10000 - 6250 cm**(-1)

Suhrmann; Klein; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 50; (1941); p. 35; Atti X. Congr. int. Chim. Rom 1938; vol. Bd.; p. 2 S. 525, 529, View in Reaxys 28 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1429 - 500 cm**(-1)

Lecomte; Journal de Physique et le Radium; vol. <7> 8; (1937); p. 489,492, View in Reaxys; Lecomte; Freymann; Bulletin de la Societe Chimique de France; vol. <5> 8; (1941); p. 612,616, View in Reaxys 29 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Comment (IR Spectroscopy)

500 - 200 cm**(-1)

Barchewitz; Parodi; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 207; (1938); p. 903; Journal de Physique et le Radium; vol. <7> 10; (1939); p. 143,150, View in Reaxys 30 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

10000 - 769 cm**(-1)

Plum; Journal of Chemical Physics; vol. 5; (1937); p. 174, View in Reaxys 31 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

11111 - 9091 cm**(-1)

Freymann; Naherniac; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 197; (1933); p. 829; Journal de Physique et le Radium; vol. <7> 5; (1934); p. 75,77, View in Reaxys 32 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

12500 - 8333 cm**(-1)

Freymann; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 194; (1932); p. 1471; Annales de Physique (Paris, France); vol. <10> 20; (1933); p. 243,289, View in Reaxys 33 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

10000 - 1333 cm**(-1)

Daugherty; Physical Review; vol. <2> 34; (1929); p. 1549,1552, View in Reaxys 34 of 37

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

von fluessigem und gasfoermigem Jodbenzol.

Purvis; Pr. Cambridge phil. Soc.; vol. 21; p. 561; Chem. Zentralbl.; vol. 94; nb. III; (1923); p. 979, View in Reaxys 35 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

714 - 417 cm**(-1)

A.P.I. Res. Project 44 Nr. 1291, 1292 <1952>, View in Reaxys 36 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

5000 - 667 cm**(-1)

A.P.I. Res. Project 44 Nr. 1291, 1292 <1952>, View in Reaxys 37 of 37

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

CS2

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Comment (IR Spectroscopy)

5000 - 667 cm**(-1)

A.P.I. Res. Project 44 Nr. 1291, 1292 <1952>, View in Reaxys Mass Spectrometry (27) Description (Mass Location Spectrometry)

Comment (Mass Spectrometry)

References

spectrum

Wilson, Stephen R.; Jacob, Linda A.; Journal of Organic Chemistry; vol.

51; nb. 25; (1986); p. 4833 - 4836, View in Reaxys; Hywei Evans; Pretorlus, Warren; Ebdon, Les; Rowland, Steve; Analytical Chemistry; vol. 66; nb. 20; (1994); p. 3400 - 3407, View in Reaxys; Cheng, P.Y.; Zhong, D.; Zewail, Ahmed H.; Chemical Physics Letters; vol. 237; nb. 5,6; (1995); p.

399 - 405, View in Reaxys; Matsumoto, Junichi; Lin, Cheng-Huang; Imasaka, Totaro; Analytical Chemistry; vol. 69; nb. 22; (1997); p. 4524 4529, View in Reaxys; Zhong, Dongping; Zewail, Ahmed H.; Journal of Physical Chemistry A; vol. 102; nb. 23; (1998); p. 4031 - 4058, View in Reaxys; Xu, Bingjun; Madix, Robert J.; Friend, Cynthia M.; Physical Chemistry Chemical Physics; vol. 15; nb. 9; (2013); p. 3179 3185, View in Reaxys; Zhang, Xiaoyan; Sun, Zaicheng; Wang, Bin; Tang, Yu; Nguyen, Luan; Li, Yuting; Tao, Franklin Feng; Journal of the American Chemical Society; vol. 140; nb. 3; (2018); p. 954 - 962, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); spectrum

Liao, Ching-Wen; Lin, Yeh-Sheng; Chanda, Kaushik; Song, Yen-Fang; Huang, Michael H.; Journal of the American Chemical Society; vol. 135; nb. 7; (2013); p. 2684 - 2693, View in Reaxys; Choe, Cholho; Yang, Ling; Lv, Zhanao; Mo, Wanling; Chen, Zhuqi; Li, Guangxin; Yin, Guochuan; Dalton Transactions; vol. 44; nb. 19; (2015); p. 9182 - 9192, View in Reaxys; Mi, Chun; Li, Lu; Meng, Xiang-Guang; Yang, RenQiang; Liao, Xiao-Hong; Tetrahedron; vol. 72; nb. 42; (2016); p. 6705 6710, View in Reaxys; Liu, Wenbo; Yang, Xiaobo; Gao, Yang; Li, ChaoJun; Journal of the American Chemical Society; vol. 139; nb. 25; (2017); p.

8621 - 8627, View in Reaxys

gas chromatography mass spectrometry (GCMS); spectrum

Bergström, Maria; Suresh, Ganji; Naidu, Veluru Ramesh; Unelius, C. Rikard; European Journal of Organic Chemistry; vol. 2017; nb. 22; (2017); p. 3234 - 3239, View in Reaxys

electron impact (EI); spectrum

Page/Page column 17

Patent; UNIVERSITY OF GUELPH; Denk, Michael K.; Milutinovic, Nicholas; Marczenko, Katherine; (14 pag.); US9744392; (2017); (B1) English, View in Reaxys

APCI (atmospheric pressure chemical ionization); spectrum

supporting information

Ahmed-Omer, Batool; Sliwinski, Eric; Cerroti, John P.; Ley, Steven V.; Organic Process Research and Development; vol. 20; nb. 9; (2016); p. 1603 - 1614, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); IT (ion trap); spectrum

Chen, Jing; Chen, Chao; Chen, Junjie; Wang, Guohua; Qu, Hongmei; Chemical Communications; vol. 51; nb. 7; (2015); p. 1356 - 1359, View in Reaxys

spectrum

supporting information

Yang, Hengquan; Fu, Luman; Wei, Lijuan; Liang, Jifen; Binks, Bernard P.; Journal of the American Chemical Society; vol. 137; nb. 3; (2015); p. 1362 - 1371, View in Reaxys

electrospray ionisa- supporting information (ESI); spection trum

Srinivas; Rawat, Vikas S.; Sreedhar, Bojja; Advanced Synthesis and Catalysis; vol. 357; nb. 16-17; (2015); p. 3587 - 3596, View in Reaxys; Zhu, Hui; Zhang, Shusheng; Wang, Haoyang; Xu, Bin; Guo, Yinlong; Chinese Journal of Chemistry; vol. 33; nb. 12; (2015); p. 1365 - 1370, View in Reaxys

gas chromatograsupporting informaphy mass spectrom- tion etry (GCMS); timeof-flight mass spectra (TOFMS); electron impact (EI); spectrum

Zhu, Hui; Zhang, Shusheng; Wang, Haoyang; Xu, Bin; Guo, Yinlong; Chinese Journal of Chemistry; vol. 33; nb. 12; (2015); p. 1365 - 1370, View in Reaxys

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2018-06-17 20:23:57

spectrum

Paragraph 0251

Patent; Duksan neolux co. ltd.; Park, Jong Hwan; Lee, Son Hui; Moon, Song Yoon; Kim, Dae Song; Jong, Hwa Soon; Kim, Won Sam; Pyeon, Ji Hoon; Lee, Bom Song; (110 pag.); KR101497124; (2015); (B1) Korean, View in Reaxys

spectrum

Paragraph 0179

Patent; Duksan Neolux Co., Ltd.; Samsung Display Co., Ltd; Park, Jong Hwan; Lee, Son Hee; Mun, Song Yun; Kim, Dae Song; Jong, Hwa Sun; Kim, Won Sam; Pyeon, Ji Hun; Lee, Bom Song; Choe, Dae Hyuk; Kim, Dong Ha; (74 pag.); KR101498278; (2015); (B1) Korean, View in Reaxys

electron impact (EI); spectrum

supporting information

Niu, Liting; Zhang, Hao; Yang, Haijun; Fu, Hua; Synlett; vol. 25; nb. 7; (2014); p. 995 - 1000; Art.No: 691, View in Reaxys

EI (Electron impact); Spectrum

LCMS (Liquid chromatography mass spectrometry)

Yao, Shengjun; Zhang, Xiang; Zhou, Jing; Qian, Rong; Xu, Zhe; Fang, Fang; Wei, Yuanlong; Wang, Cuihong; Yuan, Shuai; Guo, Yinlong; Journal of Mass Spectrometry; vol. 44; nb. 1; (2009); p. 32 - 39, View in Reaxys; Sheshenev, Andrey E.; Baird, Mark S.; Croft, Anna K.; Bolesov, Ivan G.; Tetrahedron; vol. 65; nb. 48; (2009); p. 10036 - 10046, View in Reaxys; Yang, Haijun; Li, Yong; Jiang, Min; Wang, Junmei; Fu, Hua; Chemistry - A European Journal; vol. 17; nb. 20; (2011); p. 5652 5660, View in Reaxys Page/Page column 36

Patent; Chen, Li; Feng, Lichun; Huang, Mengwei; Liu, Yongfu; Wu, Guolong; Wu, Jim Zhen; Zhou, Mingwei; US2011/257151; (2011); (A1) English, View in Reaxys

EI (Electron impact); TOFMS (Time of flight mass spectrum); Spectrum

Tranter, Robert S.; Klippenstein, Stephen J.; Harding, Lawrence B.; Giri, Binod R.; Yang, Xueliang; Kiefer, John H.; Journal of Physical Chemistry A; vol. 114; nb. 32; (2010); p. 8240 - 8261, View in Reaxys

HRMS (High resolution mass spectrometry); EI (Electron impact); Spectrum

Hashmi, A. Stephen K.; Ramamurthi, Tanuja Dondeti; Todd, Matthew H.; Tsang, Althea S.-K.; Graf, Katharina; Australian Journal of Chemistry; vol. 63; nb. 12; (2010); p. 1619 - 1626, View in Reaxys

spectrum; electron impact (EI)

Prata, Jose V.; Clemente, Dina-Telma S.; Prabhakar, Sundaresan; Lobo, Ana M.; Mourato, Isabel; Branco, Paula S.; Journal of the Chemical Society. Perkin Transactions 1; nb. 4; (2002); p. 513 - 528, View in Reaxys

spectrum; time-offlight mass spectra (TOFMS)

Friderichsen; Radziszewski; Nimlos; Winter; Dayton; David; Ellison; Journal of the American Chemical Society; vol. 123; nb. 9; (2001); p. 1977 1988, View in Reaxys; Kadi; Davidsson; Tarnovsky; Rasmusson; Akesson; Chemical Physics Letters; vol. 350; nb. 1-2; (2001); p. 93 - 98, View in Reaxys; Lobo; Vieira, P. Limao; Godinho; Calhorda; Journal of Chemical Physics; vol. 116; nb. 22; (2002); p. 9712 - 9720, View in Reaxys

spectrum; chemical ionization (CI)

Vairamani, M.; Organic Mass Spectrometry; vol. 28; nb. 12; (1993); p.

1498 - 1503, View in Reaxys

electron impact (EI); spectrum

Villa, E.; Dagata, J. A.; Lin, M. C.; Journal of Chemical Physics; vol. 92; nb. 2; (1990); p. 1407 - 1412, View in Reaxys laser desorption

Szaflarski, Diane M.; Berg, R. van den; El-Sayed, M. A.; Journal of Physical Chemistry; vol. 93; nb. 18; (1989); p. 6700 - 6704, View in Reaxys

negative ion spectroscopy

Olthoff, James K.; Tossell, John A.; Moore, John H.; Journal of Chemical Physics; vol. 83; nb. 11; (1985); p. 5627 - 5634, View in Reaxys

fragmentation pattern; spectrum; electron impact (EI)

Newton, Kenneth R.; Bernstein, Richard B.; Journal of Physical Chemistry; vol. 87; nb. 12; (1983); p. 2246 - 2255, View in Reaxys

fragmentation pattern; chemical ionization (CI); spectrum

Luijten, W. C. M. M.; Onkenhout, W.; Thuijl, J. van; Organic Mass Spectrometry; vol. 15; nb. 7; (1980); p. 329 - 330, View in Reaxys

Subba Rao; Fenselau; Analytical Chemistry; vol. 50; (1978); p. 511, View in Reaxys; Johnstone; Mellon; Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics; vol. 68; (1972); p.

1209, View in Reaxys; Bouchoux; Organic Mass Spectrometry; vol. 12;

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(1977); p. 681, View in Reaxys; Howe; Williams; Journal of the American Chemical Society; vol. 91; (1969); p. 7137,7141, View in Reaxys; Leung; Harrison; Journal of the American Chemical Society; vol. 101; (1979); p.

3168,3172, View in Reaxys; Martinsen; Buttrill; Organic Mass Spectrometry; vol. 11; (1976); p. 762,767, View in Reaxys; Leung; Harrison; Canadian Journal of Chemistry; vol. 54; (1976); p. 3439,3441,3443, View in Reaxys; Behan et al.; Organic Mass Spectrometry; vol. 11; (1976); p. 207,208, View in Reaxys; Williams; Bowen; Organic Mass Spectrometry; vol. 11; (1976); p. 223,224, View in Reaxys; Facchetti et al.; Chimica e l'Industria (Milan, Italy); vol. 51; (1969); p. 1373, View in Reaxys; Howe; Williams; Organic Mass Spectrometry; vol. 2; (1969); p. 1141, View in Reaxys; McLafferty; Analytical Chemistry; vol. 34; (1962); p.

16,23, View in Reaxys; Kurz; Hage; Journal of Organic Chemistry; vol. 42; (1977); p. 4080, View in Reaxys; Stapleton et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 1219,1220, View in Reaxys; Bentley et al.; Journal of the American Chemical Society; vol. 91; (1969); p. 3978, View in Reaxys appearance potentials fragmentation pattern

Yeo; Williams; Journal of the Chemical Society [Section] D: Chemical Communications; (1970); p. 886, View in Reaxys Elektronenstoss

Momigny; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p.

144,166; Ann. Soc. scient. Bruxelles; vol. # 71; (1957); p. 66, View in Reaxys

UV/VIS Spectroscopy (33) 1 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Absorption Maxima (UV/ VIS) [nm]

225

Nekipelova, Tatiana D.; Kuzmin, Vladimir A.; Matveeva, Elena D.; Gleiter, Rolf; Zefirov, Nikolay S.; Journal of Physical Organic Chemistry; vol. 26; nb. 2; (2013); p. 137 - 143, View in Reaxys 2 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

water

Location

supporting information

Xu, Daqian; Wang, Shoufeng; Shen, Zhiqiang; Xia, Chungu; Sun, Wei; Organic and Biomolecular Chemistry; vol. 10; nb.

14; (2012); p. 2730 - 2732, View in Reaxys 3 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Schaufele; Goodman; Transactions of the Faraday Society; vol. 61; (1965); p. 597,598, View in Reaxys; Lisitza et al.; Molecular Crystals; vol. 28; (1974); p. 161,164, View in Reaxys; Lisitsa; Ralko; Optics and Spectroscopy; vol. 24; (1968); p. 284; ; p.

540, View in Reaxys; Dzvonik et al.; Journal of Chemical Physics; vol. 61; (1974); p. 4408,4414, View in Reaxys; Kimura; Nagakura; Molecular Physics; vol. 9; (1965); p. 117,120, View in Reaxys; Hoz; Bunnett; Journal of the American Chemical Society; vol. 99; (1977); p. 4690,4692-4694, View in Reaxys; Forbes; Canadian Journal of Chemistry; vol. 39; (1961); p.

2295,2300, View in Reaxys; Dearden; Forbes; Canadian Journal of Chemistry; vol. 38; (1960); p. 896,904, View in Reaxys; Dearden; Journal of Organic Chemistry; vol. 29; (1964); p. 1821,1825, View in Reaxys; Basinski; Latowski; Roczniki Chemii; vol. 36; (1962); p. 513,514,517; Chem.Abstr.; vol. 57; nb. 13329g; (1963), View in Reaxys; Obuya, Emilly A.; Harrigan, William; Andala, Dickson M.; Lippens, Jennifer; Keane, Thomas C.; Jones Jr., Wayne E.; Journal of Molecular Catalysis A: Chemical; vol. 340; nb. 1-2; (2011); p. 89 - 98, View in Reaxys 4 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

Hillmer; Paersch; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <A> 161; (1932); p. 46,56, View in Reaxys; ConradBillroth; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 25; (1934); p. 139,150, View in Reaxys; Klingstedt; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 20; (1933); p. 125,126, View in Reaxys; Senapati, Dulal; Das, Puspendu K.; Chemical Physics Letters; vol. 402; nb. 4-6; (2005); p. 450 - 454, View in Reaxys 5 of 33

Solvent (UV/VIS Spectroscopy)

cyclohexane

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Absorption Maxima (UV/ VIS) [nm]

257

Senapati, Dulal; Maity, Sandip; Das, Puspendu K.; Journal of Physical Chemistry A; vol. 108; nb. 39; (2004); p. 7949 - 7953, View in Reaxys 6 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Forbes; Canadian Journal of Chemistry; vol. 37; (1959); p. 1977,1981, View in Reaxys; Senapati, Dulal; Maity, Sandip; Das, Puspendu K.; Journal of Physical Chemistry A; vol. 108; nb. 39; (2004); p. 7949 - 7953, View in Reaxys 7 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Kavita; Das, Puspendu K.; Journal of Chemical Physics; vol. 117; nb. 5; (2002); p. 2038 - 2044, View in Reaxys 8 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

acetonitrile

Comment (UV/VIS Spectroscopy)

Remark: deg 20 C

Bykowski, Darren; McDonald, Robert; Hinkle, Robert J.; Tykwinski, Rik R.; Journal of Organic Chemistry; vol. 67; nb. 9; (2002); p. 2798 - 2804, View in Reaxys 9 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Comment (UV/VIS Spectroscopy)

240 - 320 nm

Freitas, John E.; El-Sayed, Mostafa A.; Hwang, Hyun Jin; Journal of Physical Chemistry; vol. 99; nb. 19; (1995); p. 7395 7406, View in Reaxys 10 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Absorption Maxima (UV/ VIS) [nm]

256.5

Ext./Abs. Coefficient [l·mol-1cm-1]

748

Fugaeva, O.M.; Korobeinicheva, I.K.; Bardin, V.V.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 40; nb. 11; (1991); p. 2309 - 2311; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 11; (1991); p. 2637 - 2639, View in Reaxys 11 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

CH2Cl2

Comment (UV/VIS Spectroscopy)

250 - 450 nm

Shiraki, Shinji; Yamamoto, Yukio; Hayashi, Koichiro; Bulletin des Societes Chimiques Belges; vol. 99; (1990); p. 951 - 956, View in Reaxys 12 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

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Absorption Maxima (UV/ VIS) [nm]

257

Takuma; Deguchi; Sanemasa; Bulletin of the Chemical Society of Japan; vol. 63; nb. 4; (1990); p. 1246 - 1248, View in Reaxys 13 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Absorption Maxima (UV/ VIS) [nm]

253; 219

Selavka; Krull; Analytical chemistry; vol. 59; nb. 22; (1987); p. 2704 - 2709, View in Reaxys 14 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

275 - 650 nm

Fox, Marye Anne; Younathan, Janet; Fryxell, Glen E.; Journal of Organic Chemistry; vol. 48; nb. 18; (1983); p. 3109 - 3112, View in Reaxys 15 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

185 - 400 nm

Pence, William H.; Baughcum, Steven L.; Leone, Stephen R.; Journal of Physical Chemistry; vol. 85; nb. 25; (1981); p. 3844 - 3851, View in Reaxys 16 of 33

Description (UV/VIS Spectroscopy)

UV/VIS

Shorygin et al.; Russian Journal of Physical Chemistry; vol. 42; (1968); p. 555,556; ; p. 1057, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Walkley; Journal of Chemical Physics; vol. 33; (1960); p. 621, View in Reaxys; Deich; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 975,891, View in Reaxys; Diedrich et al.; Canadian Journal of Chemistry; vol. 50; (1972); p. 1743,1747, View in Reaxys; Miskevitch; Gutorova; Sov. Prog. Chem. (Engl. Transl.); vol. 39; nb. 1; (1973); p. 82,80, View in Reaxys; Beg; Abbasi; Pakistan Journal of Scientific and Industrial Research; vol. 12; (1969); p. 12, View in Reaxys; Beringer; Lillien; Journal of the American Chemical Society; vol. 82; (1960); p. 5135,5137, View in Reaxys; Karaianev et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 6474, View in Reaxys; Dunbar et al.; Journal of the American Chemical Society; vol. 101; (1979); p.

6506,6507,6508, View in Reaxys 17 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Vesala; Acta Chemica Scandinavica, Series A: Physical and Inorganic Chemistry; vol. 28; (1974); p. 839,841, View in Reaxys; Gakovic; Morgan; Journal of the Chemical Society [Section] B: Physical Organic; (1967); p. 416, View in Reaxys; Schindlbauer; Monatshefte fuer Chemie; vol. 94; (1963); p. 99,105, View in Reaxys; Bonnafous et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 462, View in Reaxys 18 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

hexane; ethanol

Absorption Maxima (UV/ VIS) [nm]

227.5

Burawoy; Thompson; Journal of the Chemical Society; (1956); p. 4314,4316, View in Reaxys 19 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

hexane; ethanol

Absorption Maxima (UV/ VIS) [nm]

230

Burawoy; Thompson; Journal of the Chemical Society; (1956); p. 4314,4316, View in Reaxys 20 of 33

Description (UV/VIS Spectroscopy)

Spectrum

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Solvent (UV/VIS Spectroscopy)

heptane

Nagakura; Tanaka; Journal of Chemical Physics; vol. 22; (1954); p. 236,240, View in Reaxys 21 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

325 - 400 nm; feste Loesung in Petrolaether bei -180grad.

Ferguson; Iredale; Journal of the Chemical Society; (1953); p. 2959,2963, View in Reaxys 22 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

200 - 300 nm; bei Raumtemperatur.

Ungnade; Journal of the American Chemical Society; vol. 75; (1953); p. 432, View in Reaxys 23 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. ethanol

Comment (UV/VIS Spectroscopy)

200 - 300 nm; bei Raumtemperatur.

Ungnade; Journal of the American Chemical Society; vol. 75; (1953); p. 432, View in Reaxys 24 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol; H2O

Comment (UV/VIS Spectroscopy)

200 - 300 nm; bei Raumtemperatur.

Ungnade; Journal of the American Chemical Society; vol. 75; (1953); p. 432, View in Reaxys 25 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Ley; v. Engelhardt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 74; (1910); p. 33, View in Reaxys; Purvis; Journal of the Chemical Society; vol. 99; (1911); p. 2318,2323, View in Reaxys; AZOUZ; PARKE; WILLIAMS; The Biochemical journal; vol. 50; nb. 5; (1952); p. 702 - 706, View in Reaxys; Bowden; Braude; Journal of the Chemical Society; (1952); p. 1068,1070, View in Reaxys 26 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Comment (UV/VIS Spectroscopy)

dampffoermig, bei Raumtemperatur.

Absorption Maxima (UV/ VIS) [nm]

272.1

Dunn; Iredale; Journal of the Chemical Society; (1952); p. 1592,1595, View in Reaxys 27 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

light petroleum

Comment (UV/VIS Spectroscopy)

feste Loesung bei -183grad.

Absorption Maxima (UV/ VIS) [nm]

275.2

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Dunn; Iredale; Journal of the Chemical Society; (1952); p. 1592,1595, View in Reaxys 28 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Comment (UV/VIS Spectroscopy)

dampffoermig, bei Raumtemperatur.

Absorption Maxima (UV/ VIS) [nm]

250.2; 254.7; 261.3; 268.3

Dunn; Iredale; Journal of the Chemical Society; (1952); p. 1592,1595, View in Reaxys 29 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

light petroleum

Comment (UV/VIS Spectroscopy)

feste Loesung bei -183grad.

Absorption Maxima (UV/ VIS) [nm]

257.6; 264.3; 267.9; 271.4

Dunn; Iredale; Journal of the Chemical Society; (1952); p. 1592,1595, View in Reaxys 30 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

hexane

Comment (UV/VIS Spectroscopy)

Dampf.

Durie et al.; Journal of the Chemical Society; (1950); p. 1181,1183, View in Reaxys 31 of 33

Description (UV/VIS Spectroscopy)

Absorption maxima

Comment (UV/VIS Spectroscopy)

im fernen UV (120-270 mμ).

Price; Walsh; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol.

191; (1947); p. 22,29, 30, View in Reaxys 32 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

des Dampfes.

Purvis; Journal of the Chemical Society; vol. 99; (1911); p. 2318,2323, View in Reaxys 33 of 33

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

der Fluessigkeit.

Purvis; Journal of the Chemical Society; vol. 99; (1911); p. 2318,2323, View in Reaxys ESR Spectroscopy (3) 1 of 3

Description (ESR Spectro- ESR-hyperfine coupling constants scopy) Solvents (ESR Spectrosco- CCl3F py) Comment (ESR Spectroscopy)

127I.

Maj, Paul; Hasegawa, Akinori; Symons, Martyn C. R.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 79; (1983); p. 1931 - 1938, View in Reaxys 2 of 3

Description (ESR Spectro- g-factor scopy)

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Maj, Paul; Hasegawa, Akinori; Symons, Martyn C. R.; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 79; (1983); p. 1931 - 1938, View in Reaxys 3 of 3

Description (ESR Spectro- ESR scopy) Buick et al.; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1969); p. 666, View in Reaxys; Noda et al.; Bulletin of the Chemical Society of Japan; vol. 41; (1968); p. 2882, View in Reaxys

NQR Spectroscopy (3) Description (NQR Nucleus (NQR Spectroscopy) Spectroscopy)

References

Nuclear quadrupole resonance

Semin; Journal of Structural Chemistry; vol. 2; (1961); p. 347; Zhurnal Strukturnoi Khimii; vol. 2; (1961); p. 370, View in Reaxys; Petukhov, S. A.; Bryukhova, E. V.; Semin, G. K.; Biguslavskii, A. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; nb. 7; (1984); p. 1389 - 1394; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 7; (1984); p. 1511 - 1517, View in Reaxys; Semin, G. K.; Gushchin, S. I.; Stanko, V. I.; Bryukhova, E. V.; Iroshnikova, N. G.; Doklady Chemistry; vol. 281; (1985); p. 121 125; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 281; nb. 5; (1985); p. 1126 - 1130, View in Reaxys

Nuclear quadrupole 127I coupling constants

Semin, G.K.; Gushchin, S.I.; Petukhov, S.A.; Grushin, V.V.; Tolstaya, T.P.; Lisichkina, I.N.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; nb. 11; (1984); p. 2401 - 2402; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 11; (1984); p. 2622 - 2623, View in Reaxys

Nuclear quadrupole coupling constants

Ehrlich; Kaplan; Journal of Chemical Physics; vol. 54; (1971); p. 612,615, 616, View in Reaxys

Rotational Spectroscopy (1) Description (Rota- References tional Spectroscopy) Microwave spectrum

Steinmetz; Journal of the American Chemical Society; vol. 96; (1974); p. 685,687, 689, View in Reaxys; Mirri; Caminati; Chemical Physics Letters; vol. 8; (1971); p. 409, View in Reaxys; Johansson et al.; Arkiv foer Fysik; vol. 29; (1965); p. 531, View in Reaxys

Raman Spectroscopy (13) Description (Ram- Solvent (Raman an Spectroscopy) Spectroscopy)

Comment (Raman Spectroscopy)

Spectrum; Bands

Bartual-Murgui, Carlos; Akou, Amal; Shepherd, Helena J.; Molnar, Gabor; Real, J. Antonio; Salmon, Lionel; Bousseksou, Azzedine; Chemistry - A European Journal; vol. 19; nb. 44; (2013); p. 15036 - 15043, View in Reaxys

Bands

1-methyl-pyrrolidin-2-one

Spectrum

solid

Bands

References

in the presence of organic compounds

Aarnoutse, Petra J.; Westerhuis, Johan A.; Analytical Chemistry; vol. 77; nb. 5; (2005); p. 1228 - 1236, View in Reaxys Bartolini, Paolo; Journal of Chemical Physics; vol. 110; nb. 17; (1999); p.

8653 - 8662, View in Reaxys

acetic acid

Spectrum

Copyright © 2018 Reed Elsevier Properties SA. All rights reserved. Authorized use only.

Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

Brazdil, Linda C.; Cutler, Carlo J.; Journal of Organic Chemistry; vol. 61; nb. 26; (1996); p. 9621 - 9622, View in Reaxys; Brazdil, Linda C.; Fitch, Jill L.; Cutler, Carlo J.; Haynik, Denise M.; Ace, Eryn R.; Journal of the Chemical Society. Perkin Transactions 2; nb. 4; (1998); p. 933 - 936, View in Reaxys Kahovec; Reitz; Monatshefte fuer Chemie; vol. 69; (1936); p. 363,373, View in Reaxys; Murray; Andrews; Journal of Chemical Physics; vol. 1; (1933); p. 406,408, 411, View in Reaxys; Kohlrausch; Naturwissenschaften; vol. 25; (1937); p. 635; Monatshefte fuer Chemie; vol. 76; (1947); p.

231,240, View in Reaxys; Kohlrausch; Wittek; Monatshefte fuer Chemie; vol. 74; (1943); p. 24, View in Reaxys; Dadieu; Kohlrausch; Monatshefte fuer Chemie; vol. 57; (1931); p. 488,499, View in Reaxys; Wittek; Monatshefte fuer Chemie; vol. 73; (1941); p. 231,240; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. <B> 52; (1942); p. 315,318, View in Reaxys; McDevitt; Fateley; Journal of Molecular Structure; vol. 5; (1970); p.

477,484, View in Reaxys; Schmidt; Brova; Berichte der Bunsen-Gesellschaft; vol. 75; (1971); p. 1334,1336,1338,1342, View in Reaxys; Clark; Mc Caffery; Journal of Physical Chemistry; vol. 81; (1977); p. 1918,1922, View in Reaxys; Meneely et al.; Journal of Molecular Spectroscopy; vol.

39; (1971); p. 73,76, View in Reaxys; Dumas et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie B: Sciences Physiques; vol. 267;

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(1968); p. 267, View in Reaxys; Kung, Chung-Yi; Chang, Bor-Yu; Kittrell, C.; Johnson, Bruce R.; Kinsey, James L.; Journal of Physical Chemistry; vol. 97; nb. 10; (1993); p. 2228 - 2235, View in Reaxys Raman resonance effect

O'Brien, Sean C.; Kittrell, Carter; Kinsey, James L.; Johnson, Bruce R.; Journal of Chemical Physics; vol. 96; nb. 1; (1992); p. 67 - 76, View in Reaxys; Kung, Chung-Yi; Chang, Bor-Yu; Kittrell, C.; Johnson, Bruce R.; Kinsey, James L.; Journal of Physical Chemistry; vol. 97; nb. 10; (1993); p. 2228 - 2235, View in Reaxys

Spectrum

gaseous matrix

O'Brien, Sean C.; Kittrell, Carter; Kinsey, James L.; Johnson, Bruce R.; Journal of Chemical Physics; vol. 96; nb. 1; (1992); p. 67 - 76, View in Reaxys

Bands

gaseous matrix

O'Brien, Sean C.; Kittrell, Carter; Kinsey, James L.; Johnson, Bruce R.; Journal of Chemical Physics; vol. 96; nb. 1; (1992); p. 67 - 76, View in Reaxys

Bands

Sidorov et al.; Optics and Spectroscopy; vol. 19; (1965); p. 116; ; p. 206, View in Reaxys; Fugaeva, O.M.; Korobeinicheva, I.K.; Bardin, V.V.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 40; nb. 11; (1991); p. 2309 - 2311; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 11; (1991); p. 2637 2639, View in Reaxys

Raman intensities

Schorygin; Egorowa; Doklady Akademii Nauk SSSR; vol. 117; (1957); p.

856,857; Doklady Chemistry; 112-117 <1957> 785, 786, View in Reaxys; Yoshino; Bl. Tokyo Inst. Technol.; vol. <A>; (1957); p. 303,352, 353; Chem.Abstr.; (1959); p. 4900, View in Reaxys; Sidorov et al.; Optics and Spectroscopy; vol. 19; (1965); p. 116; ; p. 206, View in Reaxys; Korobeinicheva, I. K.; Fugaeva, O. M.; Furin, G. G.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 36; nb. 8; (1987); p. 1634 - 1637; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 8; (1987); p. 1766 - 1769, View in Reaxys

Bands

acetone

Korobeinicheva, I. K.; Fugaeva, O. M.; Furin, G. G.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 36; nb. 8; (1987); p. 1634 - 1637; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 8; (1987); p. 1766 - 1769, View in Reaxys

Raman

Nevzorov; Sechkarev; Sov. Phys. J. (Engl. Transl.); vol. 14; nb. 2; (1971); p. 75,199, View in Reaxys; Sechkarev; Dvorovenko; Sov. Phys. J. (Engl.

Transl.); vol. 9; nb. 2; (1966); p. 7,1, View in Reaxys; Sechkaryov; Optics and Spectroscopy; vol. 19; (1965); p. 401; ; p. 721, View in Reaxys; ElSayed et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p. 227, View in Reaxys; Hikal et al.; Spectroscopy Letters; vol. 2; (1969); p. 13,15, View in Reaxys; Horak; Vitek; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1107,1109-1116, View in Reaxys; Sechkarev; Dvorovenko; Sov. Phys. J. (Engl. Transl.); vol.

1; (1965); p. 13,7,10, View in Reaxys

Degree of depolarization of Raman bands

Sidorov et al.; Optics and Spectroscopy; vol. 19; (1965); p. 116; ; p. 206, View in Reaxys

Luminescence Spectroscopy (5) Description (Lumi- Location nescence Spectroscopy) X-ray spectroscopy

References

supporting informa- Wegeberg, Christina; Frankær, Christian Grundahl; McKenzie, Christine J.; Dalton Transaction tions; vol. 45; nb. 44; (2016); p. 17714 - 17722, View in Reaxys

Luminescence quenching

Gray et al.; Journal of Chemical Physics; vol. 48; (1968); p. 1145,1148, View in Reaxys; Roundhill, D. Max; Shen, Zhong-Ping; King, Christopher; Atherton, Stephen J.; Journal of Physical Chemistry; vol. 92; nb. 14; (1988); p. 4088 - 4094, View in Reaxys

Luminescence quantum yield

Pac et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p. 1169,1171, View in Reaxys; Pence, William H.; Baughcum, Steven L.; Leone, Stephen R.; Journal of Physical Chemistry; vol. 85; nb. 25; (1981); p. 3844 - 3851, View in Reaxys

Lasing properties

Mizugai, Yoshihiro; Katayama, Mikio; Journal of the American Chemical Society; vol. 102; nb.

21; (1980); p. 6424 - 6426, View in Reaxys

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Luminescence lifetime

Plass; Berichte der Bunsen-Gesellschaft; vol. 74; (1970); p. 343,344-346, View in Reaxys

Fluorescence Spectroscopy (5) Description (Fluo- Solvent (Fluoresrescence Spectrocence Spectroscoscopy) py)

Comment (Fluores- References cence Spectroscopy)

Fluorescence quantum yield

wavelength depend- Kavita; Das, Puspendu K.; Journal of Chemical Physics; vol. 117; nb. 5; ence (2002); p. 2038 - 2044, View in Reaxys

Spectrum

various solvent(s)

50000.01 - 12500 nm

Fluorescence

Lankers; Popp; Kiefer; Applied Spectroscopy; vol. 48; nb. 9; (1994); p.

1166 - 1168, View in Reaxys Pac et al.; Bulletin of the Chemical Society of Japan; vol. 45; (1972); p.

1169,1171, View in Reaxys

Spectrum

bei Bestrahlung mit Newcomer; Journal of the American Chemical Society; vol. 42; (1920); p.

Roentgenstrahlen.

2002, View in Reaxys

Spectrum

im Ultraviolett.

Ley; v. Engelhardt; Chemische Berichte; vol. 41; (1908); p. 2991, View in Reaxys

Other Spectroscopic Methods (2) Description (Other References Spectroscopic Methods) Photoelectron spec- Balsenc et al.; Chimia; vol. 29; (1975); p. 64, View in Reaxys; Marschner; Tetrahedron; vol. 31; (1975); p. 2303,2307, trum View in Reaxys; Boschi; Salahub; Canadian Journal of Chemistry; vol. 52; (1974); p. 1217,1220, View in Reaxys; Sell; Kuppermann; Chemical Physics; vol. 33; (1978); p. 367, View in Reaxys; Baer et al.; Journal of Chemical Physics; vol. 64; (1976); p. 2460, View in Reaxys; Cvitas et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1977); p. 962,963-965, View in Reaxys; Momigny et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 1; (1968); p. 53,55, 56, 59, 60, 62, View in Reaxys; Dunbar et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 6506,6507,6508, View in Reaxys; Mizugai, Yoshihiro; Katayama, Mikio; Journal of the American Chemical Society; vol. 102; nb. 21; (1980); p. 6424 - 6426, View in Reaxys; Fujisawa, S.; Ohno, K.; Masuda, S.; Harada, Y.; Journal of the American Chemical Society; vol. 108; nb. 21; (1986); p.

6505 - 6511, View in Reaxys; Nolan, G. S.; Saethre, L. J.; Siggel, M. R.; Thomas, T. D.; Ungier, L.; Journal of the American Chemical Society; vol. 107; nb. 23; (1985); p. 6463 - 6467, View in Reaxys; Olthoff, James K.; Tossell, John A.; Moore, John H.; Journal of Chemical Physics; vol. 83; nb. 11; (1985); p. 5627 - 5634, View in Reaxys; Mysak, Erin R.; Wilson, Kevin R.; Jimenez-Cruz, Michael; Ahmed, Musahid; Baer, Tomas; Analytical Chemistry; vol.

77; nb. 18; (2005); p. 5953 - 5960, View in Reaxys Moessbauer effect

Ehrlich; Kaplan; Journal of Chemical Physics; vol. 54; (1971); p. 612,615, 616, View in Reaxys; Lazarus; Thomas; Journal of Chemical Physics; vol. 60; (1974); p. 4682, View in Reaxys

Transport and Distribution (4) 1 of 4

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 8.56E3 - 1.81E4 l/kgHA; relative humidity affected experimental partition coefficient by up to a factor of 3

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated at least 48 h; <0.01 percent-98 percent relative humidity; 15 deg C; relative humidity effect on partition equilibrium

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 2 of 4

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - Leonardite humic acid

Results

experimental sorption enthalpy, ΔabsHi = -61.9 kJ/mol

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5 to 75 deg C

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Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 3 of 4

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 2.15E3 - 1.08E4 l/kgHA; no glass transitions below 75 deg C that had an effect on the sorption properties of humic acid as indicated by linear van't Hoff plot

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5-75 deg C; temperature dependence of partition equilibrium studied

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 4 of 4

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - snow

Results

log Ki snow surface/air (m3/m2): -3.69; Ki snow surface/air: air/snow surface sorption coefficient

Method, Remarks (Transport and Distribution)

snow from Central Swiss Alp collected on January 10, 2003; 46 deg 37' 02" N, 8 deg 35' 38" E; altitude: ca. 2278 m above sea level; sorption coefficient determined from retention volume; -6.8 deg C; inverse gas chromatography analysis

Roth, Christine M.; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 15; (2004); p. 4078 - 4084, View in Reaxys Biodegradation (1) 1 of 1

Type (Biodegradation)

anaerobic

Inoculum

estuarine sediment slurry

Half-life Time (Biodegradation)

87.7 d

Method, Remarks (Biodegradation)

sulfate-reducing sediment samples were collected at the mouth of Tsurumi River, Japan, in 1992; in screw-top test-tubes; GC/MS analysis; first-order reaction rate constant: k=0.0079 day-1

Susarla, Sridhar; Yonezawa, Yoshitaka; Masunaga, Shigeki; Water Research; vol. 32; nb. 3; (1998); p. 639 - 648, View in Reaxys Use (3) Laboratory Use and Use Pattern Handling Volatile

Location

supporting informa- Reitti, Marcus; Villo, Piret; Olofsson, Berit; Angewandte Chemie - Intertion national Edition; vol. 55; nb. 31; (2016); p. 8928 - 8932; Angew. Chem.; vol. 128; nb. 31; (2016); p. 9074 - 9078,5, View in Reaxys Carrier

Patent; MICAP PLC; WO2005/102045; (2005); (A1) English, View in Reaxys

facilitating encapsulation of the phytoactive compound within the adjuvant

Patent; MICAP PLC; WO2005/102045; (2005); (A1) English, View in Reaxys

Quantum Chemical Calculations (4) Calculated Proper- Method (Quantum ties Chemical Calculations)

Location

Dipole moment, di- Ab initio calcns. pole moment deriv- (LCAO, GO SCF, ative DIM, SAMO, X-à, Hartree-Fock) Dissociation energy, bonding energy

References

Ab initio calcns.

(LCAO, GO SCF,

References

Caminos, Daniel A.; Garro, Alexis D.; Soria-Castro, Silvia M.; Peñéñory, Alicia B.; RSC Advances; vol. 5; nb. 26; (2015); p. 20058 - 20065, View in Reaxys supporting informa- Smalley, Adam P.; Gaunt, Matthew J.; Journal of the American Chemical tion Society; vol. 137; nb. 33; (2015); p. 10632 - 10641, View in Reaxys

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DIM, SAMO, X-à, Hartree-Fock) Molecular orbitals; Electronic energy levels; Atom distances, angles

Ab initio calcns.

(LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

supporting informa- Lefevre, Guillaume; Tlili, Anis; Taillefer, Marc; Adamo, Carlo; Ciofini, tion Ilaria; Jutand, Anny; Dalton Transactions; vol. 42; nb. 15; (2013); p. 5348 - 5354, View in Reaxys

Electronic energy levels; Molecular orbitals; Atom distances, angles; Dipole moment, dipole moment derivative

Ab initio calcns.

(LCAO, GO SCF, DIM, SAMO, X-à, Hartree-Fock)

Xuesheng Zhang; Liu, Fu; Wei, Zhongbo; Wang, Zunyao; Letters in Organic Chemistry; vol. 10; nb. 1; (2013); p. 31 - 36, View in Reaxys

Medchem (17) 1 of 17

2 of 17

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1446140View in Reaxys

Substance Name

Iodobenzene

Substance Dose

0.150000 mM

Measurement Parameter

Km (Michaelis constant)

Unit

mM

Quantitative value

0.3

Measurement pX

3.52

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

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3 of 17

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1446140View in Reaxys

Substance Name

Iodobenzene

Substance Dose

0.150000 mM

Measurement Parameter

Vmax

Unit

nmol/min/mg protein

Quantitative value

6.3

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1446140View in Reaxys

Substance Name

Iodobenzene

Substance Dose

0.150000 mM

Measurement Parameter

CLint

Unit

µL/min/mg protein

Quantitative value

21

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

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4 of 17

5 of 17

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1446140View in Reaxys

Substance Name

Iodobenzene

Substance Dose

0.150000 mM

Measurement Parameter

Km (Michaelis constant)

Unit

mM

Quantitative value

0.3

Measurement pX

3.52

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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6 of 17

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1446140View in Reaxys

Substance Name

Iodobenzene

Substance Dose

0.150000 mM

Measurement Parameter

Vmax

Unit

nmol/min/mg protein

Quantitative value

6.3

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

Concomitants: Compound role

SLV; APR; COE

Target Name

Cytochrome P450 [rat]

Target Synonyms

cytochrome p450

Target, Subunit, Species

Cytochrome P450 [rat]

Target Mutant/Chimera Details

Cytochrome P450 [rat]:Wild

Target Species (Bioactivity)

rat

Target Transfection

Non Transfected

Bioassay Category

Metabolism/Transport

Bioassay Name

Enzymology substrate

Biological Species/NCBI ID

Sprague Dawley rat; Sprague Dawley rat

Organs/Tissues

liver

Cell Fraction

Microsome

Substance RN

1446140View in Reaxys

Substance Name

Iodobenzene

Substance Dose

0.150000 mM

Measurement Parameter

CLint

Unit

µL/min/mg protein

Quantitative value

21

Metabolite RN

969616; 507004; 1680024; 1362752; 1904544; 1905114; 1905112; 1905115; 1855300

Metabolite name

Phenol; p-OH-chlorobenzene; p-OH-bromobenzene; p-OH-fluorobenzene; p-OH-iodobenzene; oOH-chlorobenzene; o-OH-fluorobenzene; o-OH-bromobenzene; o-OH-iodobenzene

Concomitants: Compound RN

741857; 751311; 77911

Concomitants: Compound name

Acetonitrile; Phenobarbital; NADPH

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7 of 17

Concomitants: Compound role

SLV; APR; COE

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : bacteria, T3 mutation, 20 deg C, pH 7.0; vehicle either ν-cyclodextrin or H2O; bioluminescence measurement

Biological Species/NCBI ID

Photobacterium phosphoreum

Substance RN

1446140View in Reaxys

Substance Name

611951

Measurement Parameter

pEC50

Unit

M

Quantitative value

3.21 - 4.03

Measurement pX

4.03

Song, Wen-lu; Huang, Qing-guo; Wang, Lian-sheng; Chemosphere; vol. 38; nb. 4; (1999); p. 693 - 698, View in Reaxys 8 of 17

Substance Effect

Toxic : Acute

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Carassias auratusBioassay : temp. 20 deg C; DO 8.2 mg/l; pH 7.5; hardness as CaCO3 110 mg/l fishes ca. 3.5 g weight, 4.0 cm length; semi-static method (water renewal at each 12 h); OECD, 1984; no fed during the exposure

Substance RN

1446140View in Reaxys

Substance Name

611951

Qualitative Results

lg 1/LC 50: 5.29 (mol/l)

Measurement Parameter

qualitative

Liu; Wang; Chen; Li; Yu; Bulletin of Environmental Contamination and Toxicology; vol. 57; nb. 3; (1996); p. 421 - 425, View in Reaxys 9 of 17

Substance Effect

Antiproliferative

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Tetrahymena pyriformis GL-C, protozoaBioassay : controls: 1) no title comp., no T. pyriformis; 2) inoculated with T. pyriformis without title comp. population growth impairment testing; 40-h TETRATOX assay; population density quantitated spectrophotometrically at 540 nm

Substance RN

1446140View in Reaxys

Substance Name

611951

Measurement Parameter

pGI50

Quantitative value

0.5

Schultz, T. Wayne; Chemical Research in Toxicology; vol. 12; nb. 12; (1999); p. 1262 - 1267, View in Reaxys 10 of 17

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |protein binding Target : T4 lysozyme, L99A mutantBioassay : thermal denaturation measurements; monitored by circular dichroism or fluorescence emission; assay buffer

Substance RN

1446140View in Reaxys

Substance Name

611951

Measurement Parameter

qualitative

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Qualitative value

NA

Measurement pX

1

Graves, Alan P.; Brenk, Ruth; Shoichet, Brian K.; Journal of Medicinal Chemistry; vol. 48; nb. 11; (2005); p. 3714 - 3728, View in Reaxys 11 of 17

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : snow from Central Swiss Alp collected on January 10, 2003; 46 deg 37' 02" N, 8 deg 35' 38" E; altitude: ca. 2278 m above sea level; sorption coefficient determined from retention volume; -6.8 deg C; inverse gas chromatography analysis

Substance RN

1446140View in Reaxys

Substance Name

611951

Qualitative Results

sorption log Ki snow surface/air (m3/m2): -3.69; Ki snow surface/air: air/snow surface sorption coefficient

Measurement Parameter

qualitative

Roth, Christine M.; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 38; nb. 15; (2004); p. 4078 - 4084, View in Reaxys 12 of 17

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated at least 48 h; <0.01 percent-98 percent relative humidity; 15 deg C; relative humidity effect on partition equilibrium

Substance RN

1446140View in Reaxys

Substance Name

611951

Qualitative Results

partition Leonardite humic acid/air partition coefficient, KHA,air = 8.56E3 - 1.81E4 l/kgHA; relative humidity affected experimental partition coefficient by up to a factor of 3

Measurement Parameter

qualitative

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 13 of 17

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5 to 75 deg C

Substance RN

1446140View in Reaxys

Substance Name

611951

Qualitative Results

sorption experimental sorption enthalpy, ΔabsHi = -61.9 kJ/mol

Measurement Parameter

qualitative

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 14 of 17

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5-75 deg C; temperature dependence of partition equilibrium studied

Substance RN

1446140View in Reaxys

Substance Name

611951

Qualitative Results

partition Leonardite humic acid/air partition coefficient, KHA,air = 2.15E3 - 1.08E4 l/kgHA; no glass transitions below 75 deg C that had an effect on the sorption properties of humic acid as indicated by linear van't Hoff plot

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Measurement Parameter

qualitative

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 15 of 17

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

In vitro lethal concentration against phenobarbital induced rat hepatocytes at 2 hours incubation with compound dissolved in DMSO

Biological Species/NCBI ID

rat

Cells/Cell Lines

liver cell

Substance RN

1446140View in Reaxys

Measurement Parameter

LC50

Unit

mM

Qualitative value

=

Quantitative value

0.4

Deviation

0.01

Measurement pX

3.4

Chan, Katie; Jensen, Neil S.; Silber, Paul M.; O'Brien, Peter J.; Chemico-Biological Interactions; vol. 165; nb. 3; (2007); p.

165 - 174, View in Reaxys 16 of 17

Bioassay Category

Pharmacokinetic

Bioassay Details

In vivo concentration of the compound dissolved in DMSO required to cause liver toxicity determined by visible centrilobular necrosis at 24 h in phenobarbitol induced rat

Biological Species/NCBI ID

rat

Substance RN

1446140View in Reaxys

Measurement Parameter

concentration (parameters)

Unit

mmol/kg

Qualitative value

=

Quantitative value

0.94

Chan, Katie; Jensen, Neil S.; Silber, Paul M.; O'Brien, Peter J.; Chemico-Biological Interactions; vol. 165; nb. 3; (2007); p.

165 - 174, View in Reaxys 17 of 17

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Toxicity was measured as population growth impairment to Tetrahymena pyriformis

Biological Species/NCBI ID

Tetrahymena pyriformis

Substance RN

1446140View in Reaxys

Measurement Parameter

qualitative

Qualitative value

Not Published

Schultz, T. Wayne; Chemical Research in Toxicology; vol. 12; nb. 12; (1999); p. 1262 - 1267, View in Reaxys

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Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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