Bromoethane (Ethyl bromide; EtBr) [C2H5Br]

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Reaxys ID 1209224 View in Reaxys

1/1 CAS Registry Number: 74-96-4 Chemical Name: ethyl bromide; bromure d'ethyle; bromoethane; Aethylbromid Linear Structure Formula: BrCH2CH3 Molecular Formula: C2H5Br Molecular Weight: 108.966 Type of Substance: acyclic InChI Key: RDHPKYGYEGBMSE-UHFFFAOYSA-N Note:

Br

Substance Label (115) Label References 2a

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Tang, Qiujie; Bian, Zhaogang; Wu, Wei; Wang, Jin; Xie, Ping; Pittman, Charles U.; Zhou, Aihua; Journal of Organic Chemistry; vol. 82; nb. 19; (2017); p. 10617 - 10622, View in Reaxys

1

Semin; Petukhov; Bryukhova; Boguslavskii; Russian Chemical Bulletin; vol. 47; nb. 6; (1998); p. 1118 - 1121, View in Reaxys; Moghaddam, Firouz Matloubi; Ayati, Seyed Ebrahim; Firouzi, Hamid Reza; Ghorbani, Fereshte; Applied Organometallic Chemistry; vol. 30; nb. 6; (2016); p. 488 - 493, View in Reaxys

4a

Li, Ya; Hu, Jinbo; Journal of Fluorine Chemistry; vol. 129; nb. 5; (2008); p. 382 - 385, View in Reaxys; Cera, Gianpiero; Haven, Tobias; Ackermann, Lutz; Angewandte Chemie - International Edition; vol. 55; nb. 4; (2016); p. 1484 1488, View in Reaxys

IVa

Abbasi; Tariq; Aziz-Ur-Rehman; Siddiqui; Ahmad; Malik; Shah; Russian Journal of Bioorganic Chemistry; vol. 42; nb. 2; (2016); p. 198 - 209; Bioorg. Khim., View in Reaxys

2d

Baburajeev; Mohan, Chakrabhavi Dhananjaya; Patil, Govindagouda S.; Rangappa, Shobith; Pandey, Vijay; Sebastian, Anusha; Fuchs, Julian E.; Bender, Andreas; Lobie, Peter E.; Basappa; Rangappa, Kanchugarakoppal S.; RSC Advances; vol. 6; nb. 43; (2016); p. 36775 - 36785, View in Reaxys

10a

Xiao, Dian; Meng, Fan-Hua; Dai, Wei; Yong, Zheng; Liu, Jin-Qiu; Zhou, Xin-Bo; Li, Song; Molecules; vol. 21; nb.

4; (2016); Art.No: 488, View in Reaxys

4b

Howieson, Vanessa M.; Tran, Elisa; Hoegl, Annabelle; Fam, Han Ling; Fu, Jonathan; Sivonen, Kate; Li, Xiao Xuan; Auclair, Karine; Saliba, Kevin J.; Antimicrobial Agents and Chemotherapy; vol. 60; nb. 12; (2016); p. 7146 7152, View in Reaxys

9f

Wang, Guangfa; Bian, Linglin; Zhang, Hui; Wang, Yanhui; Gao, Lijuan; Sun, Kaiyue; Xiang, Lan; Qi, Jianhua; Chemical and Pharmaceutical Bulletin; vol. 64; nb. 2; (2016); p. 161 - 170, View in Reaxys

EB

Sobol; Engel; Rubitski; Ku; Aubrecht; Schiestl; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 633; nb. 2; (2007); p. 80 - 94, View in Reaxys; Zhu, Li-Na; Gao, Huan-Rui; Wang, Hai-Xian; Xu, Ming-Yuan; Li, Xiao-Zeng; European Journal of Inorganic Chemistry; nb. 14; (2014); p. 2396 - 2405, View in Reaxys; Arun; Packianathan; Malarvizhi; Antony; Raman; Journal of Photochemistry and Photobiology B: Biology; vol.

149; (2015); p. 93 - 102, View in Reaxys

13

Fernández-Valle, María Encarnación; Martínez-Álvarez, Roberto; Molero-Vílchez, Dolores; Pardo, Zulay D.; Sáez-Barajas, Elena; Herrera, Antonio; Journal of Organic Chemistry; vol. 80; nb. 2; (2015); p. 799 - 805, View in Reaxys

IX

Zorin; Zaynashev; Chanysheva; Russian Journal of General Chemistry; vol. 85; nb. 6; (2015); p. 1382 - 1385; Zh. Obshch. Khim.; vol. 85; nb. 6; (2015); p. 914 - 917,4, View in Reaxys

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1h

Khalili, Dariush; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 190; nb. 11; (2015); p. 1727 - 1734, View in Reaxys

-6a

Shestakov, Alexandr S.; Prezent, Mikhail A.; Zlatoustovskaya, Evgenia O.; Shikhaliev, Khidmet S.; Falaleev, Alexandr V.; Sidorenko, Oleg E.; Chemistry of Heterocyclic Compounds; vol. 51; nb. 4; (2015); p. 370 - 376; Khim.

Geterotsikl. Soedin.; vol. 51; nb. 4; (2015); p. 370 - 376,7, View in Reaxys

3a

Cutri, Christian C. C.; Garozzo, Adriana; Siracusa, Maria A.; Sarva, Maria C.; Castro, Angelo; Geremia, Ernesto; Pinizzotto, Maria R.; Guerrera, Francesco; Bioorganic and Medicinal Chemistry; vol. 7; nb. 2; (1999); p. 225 230, View in Reaxys; Lenardao, Eder J.; Mendes, Samuel R.; Ferreira, Patricia C.; Perin, Gelson; Silveira, Claudio C.; Jacob, Raquel G.; Tetrahedron Letters; vol. 47; nb. 42; (2006); p. 7439 - 7442, View in Reaxys; Dave, Chaitanya G.; Patel, Killol J.; Journal of Heterocyclic Chemistry; vol. 51; nb. 4; (2014); p. 943 - 947, View in Reaxys

1a

Gusarova; Shaikhudinova; Reutskaya; Ivanova; Tatarinova; Trofimov; Russian Chemical Bulletin; vol. 49; nb. 7; (2000); p. 1320 - 1320, View in Reaxys; Kilpin, Kelly J.; Crot, Stephanie; Riedel, Tina; Kitchen, Jonathan A.; Dyson, Paul J.; Dalton Transactions; vol. 43; nb. 3; (2014); p. 1443 - 1448, View in Reaxys

1f

De La Cerda-Pedro, Jose Emilio; Amador-Sanchez, Yoarhy Alejandro; Cortes-Hernandez, Mayra; Perez-Perez, Jovana; Rojas-Lima, Susana; Lopez-Ruiz, Heraclio; Heterocycles; vol. 89; nb. 1; (2014); p. 27 - 41, View in Reaxys

V-1-1

Patent; Shionogi and Co., Ltd.; UENAKA, Masaaki; YONEZAWA, Shuji; IIDA, Akira; TAKAKI, Mutsumi; OGAWA, Tomoyuki; GODA, Satoshi; HIROSE, Yoshikatsu; FUKUDA, Tomohiro; EP2687515; (2014); (A1) English, View in Reaxys

EtI

Patent; CALCIMEDICA, INC.; ROGERS, Evan; CAO, Jianguo; WANG, Zhijun; GREY, Jonathan; WHITTEN, Jeffrey, P.; WO2014/59333; (2014); (A1) English, View in Reaxys

XIa

Gharibyan; Makaryan; Hovhannisyan; Kinoyan; Chobanyan; Russian Journal of General Chemistry; vol. 84; nb. 3; (2014); p. 457 - 464; Zh. Obshch. Khim.; vol. 84; nb. 3; (2014); p. 399 - 406,8, View in Reaxys

R-X

Wu, Lingqiao; Song, Jinliang; Zhang, Binbin; Zhou, Baowen; Zhou, Huacong; Fan, Honglei; Yang, Yingying; Han, Buxing; Green Chemistry; vol. 16; nb. 8; (2014); p. 3935 - 3941, View in Reaxys

9a

Jin, Bo; Shen, Juan; Peng, Rufang; Chen, Congdi; Chu, Shijin; European Journal of Organic Chemistry; vol. 2014; nb. 28; (2014); p. 6252 - 6262, View in Reaxys

9k

Afri, Michal; Alexenberg, Carmit; Aped, Pinchas; Bodner, Efrat; Cohen, Sarit; Ejgenburg, Michal; Eliyahu, Shlomi; Gilinsky-Sharon, Pessia; Harel, Yifat; Naqqash, Miriam E.; Porat, Hani; Ranz, Ayala; Frimer, Aryeh A.; Chemistry and Physics of Lipids; vol. 184; (2014); p. 105 - 118, View in Reaxys

7a

Long, Brenda; Nikitin, Kirill; Fitzmaurice, Donald; Journal of the American Chemical Society; vol. 125; nb. 17; (2003); p. 5152 - 5160, View in Reaxys; McKeever, Caitriona; Kaiser, Marcel; Rozas, Isabel; Journal of Medicinal Chemistry; vol. 56; nb. 3; (2013); p. 700 - 711, View in Reaxys

3

Honaker, Matthew T.; Sandefur, Benjamin J.; Hargett, James L.; McDaniel, Alicia L.; Salvatore, Ralph Nicholas; Tetrahedron Letters; vol. 44; nb. 46; (2003); p. 8373 - 7377, View in Reaxys; Matsui, Masaki; Ooiwa, Kohtaro; Okada, Ayumi; Kubota, Yasuhiro; Funabiki, Kazumasa; Sato, Hiroyasu; Dyes and Pigments; vol. 99; nb. 3; (2013); p.

916 - 923, View in Reaxys

Et-Br

Patent; BROMINE COMPOUNDS LTD.; BEN-DAVID, Iris; MIASKOVSKI, Gershon; KOMPANIETS, Igor; WO2013/42109; (2013); (A1) English, View in Reaxys

1k

Yang, Zhanhui; Xu, Jiaxi; Synthesis (Germany); vol. 45; nb. 12; (2013); p. 1675 - 1682; Art.No: SS-2013-H0216-OP, View in Reaxys

3b

Liu, Xiao-Ling; Sheng, Shou-Ri; Wang, Qiu-Ying; Sun, Wu-Kang; Xin, Qin; Ao, Hong-Yu; Journal of Chemical Research; nb. 2; (2006); p. 118 - 120, View in Reaxys; Clark, Rachel L.; Clements, Carol J.; Barrett, Michael P.; MacKay, Simon P.; Rathnam, Rajendra P.; Owusu-Dapaah, George; Spencer, John; Huggan, Judith K.; Bioorganic and Medicinal Chemistry; vol. 20; nb. 20; (2012); p. 6019 - 6033, View in Reaxys

21

Patent; Chisso Corporation; Chisso Petrochemical Corporation; EP2279990; (2011); (A1) English, View in Reaxys

8-F

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

11

Kowalski, Piotr; Jaskowska, Jolanta; Bojarski, Andrzej J.; Duszynska, Beata; Journal of Heterocyclic Chemistry; vol. 45; nb. 1; (2008); p. 209 - 214, View in Reaxys

educt to 6

Al-Rubaie, Ali Z.; Al-Derawi, Ala'a K.; Heteroatom Chemistry; vol. 18; nb. 1; (2007); p. 93 - 99, View in Reaxys; Yadav; Somaiah; Ravindar; Chandraiah; Tetrahedron Letters; vol. 49; nb. 17; (2008); p. 2848 - 2850, View in Reaxys

RBr, n=2

Thaker; Patel, Pranay; Molecular Crystals and Liquid Crystals; vol. 482; nb. 1; (2008); p. 3 - 20, View in Reaxys

C2H5Br

Bertini, Vincenzo; Lucchesini, Francesco; Pocci, Marco; De Munno, Angela; Tetrahedron Letters; vol. 39; nb. 50; (1998); p. 9263 - 9266, View in Reaxys; Khan, Khalid A.; Moryl, Joseph E.; Slater, David A.; Lasky, Peter J.; Osgood Jr., Richard M.; Journal of Physical Chemistry B; vol. 101; nb. 44; (1997); p. 9077 - 9086, View in Reaxys; Brandsma, Lambert; Nieuwenhuizen, Willem F.; Zwikker, Jan W.; Maeeorg, Uno; European Journal of Organic Chemistry; nb. 4; (1999); p. 775 - 779, View in Reaxys; Bakunov, Stanislav A.; Rukavishnikov, Alexey V.; Tkachev,

Copyright © 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

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2018-07-24 18:37:32

Alexey V.; Synthesis; nb. 8; (2000); p. 1148 - 1159, View in Reaxys; Viggiano, Albert A.; Midey, Anthony J.; Journal of Physical Chemistry A; vol. 104; nb. 29; (2000); p. 6786 - 6790, View in Reaxys; Slivka; Khripak; Britsun; Staninets; Russian Journal of Organic Chemistry; vol. 36; nb. 7; (2000); p. 1033 - 1038, View in Reaxys; Han, Ke-Li; Zhang, Li; Xu, Da-Li; He, Guo-Zhong; Lou, Nan-Quan; Journal of Physical Chemistry A; vol. 105; nb. 13; (2001); p. 2956 - 2960, View in Reaxys; Pawlowski, Maciej; Chlon, Grazyna; Obniska, Jolanta; Zejc, Alfred; Charakchieva-Minol, Sijka; Mokrosz, Maria J.; Farmaco; vol. 55; nb. 6-7; (2000); p. 461 - 468, View in Reaxys; Dzyuba; Bartsch; Chemical Communications; nb. 16; (2001); p. 1466 - 1467, View in Reaxys; Sun, Min; Xin, Hao; Wang, KeZhi; Zhang, Yong-An; Jin, Lin-Pei; Huang, Chun-Hui; Chemical Communications; nb. 6; (2003); p. 702 - 703, View in Reaxys; Theodorou, Vassiliki; Ragoussis, Valentine; Strongilos, Alexandros; Zelepos, Evangelos; Eleftheriou, Argyro; Dimitriou, Maria; Tetrahedron Letters; vol. 46; nb. 8; (2005); p. 1357 - 1360, View in Reaxys; Morita, Yuki; Tasaka, Takeyasu; Kawabe, Kosuke; Okamoto, Hiroaki; Takenaka, Shunsuke; Kita, Hidetoshi; Molecular Crystals and Liquid Crystals; vol. 435; (2005); p. 153/[813]-162/[822], View in Reaxys; Fan, Qu-Li; Zhou, Ying; Lu, Xiao-Mei; Hou, Xiao-Yuan; Huang, Wei; Macromolecules; vol. 38; nb. 7; (2005); p. 2927 - 2936, View in Reaxys; Vicha, Robert; Necas, Marek; Potacek, Milan; Collection of Czechoslovak Chemical Communications; vol. 71; nb. 5; (2006); p. 709 - 722, View in Reaxys; Ibraev; Kozhina; Gazaliev; Fazylov; Russian Journal of Applied Chemistry; vol.

79; nb. 2; (2006); p. 329 - 330, View in Reaxys; Erdik, Ender; Kocoglu, Melike; Tetrahedron Letters; vol. 48; nb. 24; (2007); p. 4211 - 4214, View in Reaxys; Dutta, Bishnupada; Kar, Gandhi K.; Ray, Jayanta K.; Tetrahedron Letters; vol. 44; nb. 48; (2003); p. 8641 - 8643, View in Reaxys; Fang, Dong; Cheng, Jian; Gong, Kai; Shi, Qun-Rong; Zhou, Xin-Li; Liu, Zu-Liang; Journal of Fluorine Chemistry; vol. 129; nb. 2; (2008); p. 108 - 111, View in Reaxys 6c

Sun, Yuzhu; Chen, Huansheng; Li, Zhiming; Wang, Quanrui; Tao, Fenggang; Synthesis; nb. 4; (2008); p. 589 593, View in Reaxys

educt to 12

Lee, Myong Euy; Lim, Young Mook; Son, Joo Young; Seo, Won Guk; Chemistry Letters; vol. 37; nb. 7; (2008); p.

680 - 681, View in Reaxys

5 (R'=C2H5,X=Br)

Tang, Ri-Yuan; Zhong, Ping; Lin, Qiu-Lian; Phosphorus, Sulfur and Silicon and the Related Elements; vol. 182; nb.

1; (2007); p. 167 - 174, View in Reaxys

ed. to 7a,c, 8a,c

Ghorai, Manas K.; Das, Kalpataru; Kumar, Amit; Tetrahedron Letters; vol. 48; nb. 14; (2007); p. 2471 - 2475, View in Reaxys

educt to V

Matveeva; Podrugina; Grishin; Pavlova; Zefirov; Russian Journal of Organic Chemistry; vol. 43; nb. 2; (2007); p.

201 - 206, View in Reaxys

5b

Tang, Ri-Yuan; Zhong, Ping; Lin, Qiu-Lian; Synthesis; nb. 1; (2007); p. 85 - 91, View in Reaxys

2, R=Br

Kuca, Kamil; Marek, Jan; Stodulka, Petr; Musilek, Kamil; Hanusova, Petra; Hrabinova, Martina; Jun, Daniel; Molecules; vol. 12; nb. 10; (2007); p. 2341 - 2347, View in Reaxys

Ethyl-Br

Lemaire, Philippe; Balme, Genevieve; Desbordes, Philippe; Vors, Jean-Pierre; Organic and biomolecular chemistry; vol. 1; nb. 23; (2003); p. 4209 - 4219, View in Reaxys; Liu, Pingli; Huang, Liang; Faul, Margaret M.; Tetrahedron Letters; vol. 48; nb. 41; (2007); p. 7380 - 7382, View in Reaxys

1b

Tyrra, Wieland; Naumann, Dieter; Quadt, Silke; Buslei, Sigrid; Yagupolskii, Yurii L.; Kremlev, Mikhail M.; Journal of Fluorine Chemistry; vol. 128; nb. 7; (2007); p. 813 - 817, View in Reaxys

CH3CH2Br

Talybov; Nurieva; Karaev; Russian Journal of Organic Chemistry; vol. 39; nb. 8; (2003); p. 1206 - 1208, View in Reaxys; Van Delden, Richard A.; Mecca, Tommaso; Rosini, Carlo; Feringa, Ben L.; Chemistry - A European Journal; vol. 10; nb. 1; (2004); p. 61 - 70, View in Reaxys; Shashikanth; Sudha; Khanum; Heteroatom Chemistry; vol. 16; nb. 3; (2005); p. 212 - 217, View in Reaxys; Stankevic, Marek; Pietrusiewicz, K. Michal; Synthesis; nb. 8; (2005); p. 1279 - 1290; Art.No: Z00505SS, View in Reaxys; Guo, MaoJun; Varady, Laszlo; Fokas, Demosthenes; Baldino, Carmen; Yu, Libing; Tetrahedron Letters; vol. 47; nb. 23; (2006); p. 3889 - 3892, View in Reaxys; Liu, Dan; Song, Dandan; Guo, Gang; Wang, Rui; Lv, Jinling; Jing, Yongkui; Zhao, Linxiang; Bioorganic and Medicinal Chemistry; vol. 15; nb. 16; (2007); p. 5432 - 5439, View in Reaxys

educt to 8a-k

Simon, Gaelle; Couthon-Gourves, Helene; Haelters, Jean-Pierre; Corbel, Bernard; Kervarec, Nelly; Michaud, Francois; Meijer, Laurent; Journal of Heterocyclic Chemistry; vol. 44; nb. 4; (2007); p. 793 - 801, View in Reaxys

educt to 7b

Thaker; Tandel; Molecular Crystals and Liquid Crystals; vol. 451; nb. 1; (2006); p. 127 - 138, View in Reaxys; Rosiak, Anna; Frey, Wolfgang; Christoffers, Jens; European Journal of Organic Chemistry; nb. 17; (2006); p. 4044 - 4054, View in Reaxys

RX, R=Et, X=Br

Ouyang, Guiping; Zhang, Peiquan; Xu, Gangfang; Song, Baoan; Yang, Song; Jin, Linhong; Xue, Wei; Hu, Deyu; Lu, Ping; Chen, Zhuo; Molecules; vol. 11; nb. 6; (2006); p. 383 - 392, View in Reaxys

bromoethane

Lonnon, David G.; Craig, Donald C.; Colbran, Stephen B.; Dalton Transactions; nb. 31; (2006); p. 3785 - 3797, View in Reaxys

educt to 7a-d

Insuasty, Henry; Estrada, Martin; Cortes, Edward; Quiroga, Jairo; Insuasty, Braulio; Abonia, Rodrigo; Nogueras, Manuel; Cobo, Justo; Tetrahedron Letters; vol. 47; nb. 31; (2006); p. 5441 - 5443, View in Reaxys

R-CH2Br, R=CH3

Malik, Vaishalli; Singh, Palwinder; Kumar, Subodh; Tetrahedron; vol. 62; nb. 25; (2006); p. 5944 - 5951, View in Reaxys

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C

Moghaddam, Firouz Matloubi; DokhtTaimoory, Seyedeh Maryam; Ismaili, Hossein; Bardajee, Ghasem Rezanejade; Synthetic Communications; vol. 36; nb. 23; (2006); p. 3599 - 3607, View in Reaxys

educt to 5a R=Me

Raeck, Christian; Berger, Stefan; European Journal of Organic Chemistry; nb. 21; (2006); p. 4934 - 4937, View in Reaxys

educt to 8

Sabitha, Gowravaram; Bhaskar; Yadav; Tetrahedron Letters; vol. 47; nb. 46; (2006); p. 8179 - 8181, View in Reaxys

Me-CH2Br

Sibi, Mukund P.; Manyem, Shankar; Palencia, Hector; Journal of the American Chemical Society; vol. 128; nb. 42; (2006); p. 13660 - 13661, View in Reaxys

substrate to (+)-9g

Chapuis, Christian; Barthe, Michel; Cantatore, Carole; Saint-Leger, Christine; Wyss, Patrick; Helvetica Chimica Acta; vol. 89; nb. 11; (2006); p. 2638 - 2653, View in Reaxys

7b

Ramachary, Dhevalapally B.; Kishor; Reddy, G. Babul; Organic and Biomolecular Chemistry; vol. 4; nb. 9; (2006); p. 1641 - 1646, View in Reaxys

table 2, 28

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

2c

Tang, Ri-Yuan; Zhong, Ping; Lin, Qiu-Lian; Journal of Fluorine Chemistry; vol. 127; nb. 7; (2006); p. 948 - 953, View in Reaxys

educt to TEPyP

Xiliang, Guo; Shaomin, Shuang; Chuan, Dong; Feng, Feng; Wong; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 61; nb. 3; (2005); p. 413 - 418, View in Reaxys

R1X b

De Andrade, Fabiano Molinos; Massa, Werner; Peppe, Clovis; Uhl, Werner; Journal of Organometallic Chemistry; vol. 690; nb. 5; (2005); p. 1294 - 1299, View in Reaxys

4d

Sheng, Shou-Ri; Zhou, Wei; Zhong, Ming-Hua; Liu, Xiao-Ling; Chen, Hui-Zong; Synthetic Communications; vol.

35; nb. 6; (2005); p. 815 - 821, View in Reaxys

1-BrEt

Chorazewski, Miroslaw; Goralski, Pawel; Tkaczyk, Mariola; Journal of Chemical and Engineering Data; vol. 50; nb.

2; (2005); p. 619 - 624, View in Reaxys

8a

Hedfors, Asa; Appelqvist, Theresa; Carlsson, Bo; Bladh, Lars-Goeran; Litten, Chris; Agback, Peter; Grynfarb, Marlena; Koehler, Konrad F.; Malm, Johan; Journal of Medicinal Chemistry; vol. 48; nb. 9; (2005); p. 3114 - 3117, View in Reaxys

30

Salvatore, Ralph Nicholas; Smith, Robert A.; Nischwitz, Adam K.; Gavin, Terrence; Tetrahedron Letters; vol. 46; nb. 51; (2005); p. 8931 - 8935, View in Reaxys

RBr, R=C2H5

Banerjee, Tirthankar; Dureja, Prem; Molecules; vol. 10; nb. 8; (2005); p. 990 - 999, View in Reaxys

MeCH2Br

Sukhanov; Lukin; Chemistry of Heterocyclic Compounds; vol. 41; nb. 7; (2005); p. 861 - 865, View in Reaxys

CH3CH2-Br

Gmouh; Jamal-Eddine; Valnot; Tetrahedron; vol. 56; nb. 42; (2000); p. 8361 - 8366, View in Reaxys; Hahn, F. Ekkehardt; Heidrich, Beate; Luegger, Thomas; Pape, Tania; Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences; vol. 59; nb. 11-12; (2004); p. 1519 - 1523, View in Reaxys

educt to 2b

Stefanic, Petra; Breznik, Matej; Lah, Nina; Leban, Ivan; Plavec, Janez; Kikelj, Danijel; Tetrahedron Letters; vol.

42; nb. 31; (2001); p. 5295 - 5297, View in Reaxys; Chhikara, Bhupender S.; Mishra, Anil K.; Tandon, Vibha; Heterocycles; vol. 63; nb. 5; (2004); p. 1057 - 1065, View in Reaxys

7

Cohen, Richard J.; Fox, Daniel L.; Salvatore, Ralph Nicholas; Journal of Organic Chemistry; vol. 69; nb. 12; (2004); p. 4265 - 4268, View in Reaxys

Table 1, entry 2

Le, Zhang-Gao; Chen, Zhen-Chu; Hu, Yi; Zheng, Qin-Guo; Journal of Chemical Research; nb. 5; (2004); p. 344 346, View in Reaxys

BrC2H5

Millaruelo; Oriol; Serrano; Pinol; Saez; Molecular Crystals and Liquid Crystals; vol. 411; (2004); p. 451/[1493]-466/ [1508], View in Reaxys; Contoret, Adam; Eastwood, Amanda; Farrar, Simon; Kelly, Stephen M.; Nicholls, Edward; O'Neill, Mary; Richards, Gary; Wu, Catherine; Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals; vol. 368; (2001); p. 271 - 278, View in Reaxys

RCH2X; R=CH3, X=Br

Xu, Wei Ming; Tang, E; Huang, Xian; Synthesis; nb. 13; (2004); p. 2094 - 2098, View in Reaxys

RCH2Br, R = Me

Sibi, Mukund P.; Stanley, Levi M.; Tetrahedron Asymmetry; vol. 15; nb. 21; (2004); p. 3353 - 3356, View in Reaxys

educt to title comp.

Lewandowski; Swiderska; Polish Journal of Chemistry; vol. 78; nb. 9; (2004); p. 1371 - 1378, View in Reaxys

RX, R = Et, X = Br

Ovsepyan; Babakhanyan; Manukyan; Kocharyan; Russian Journal of General Chemistry; vol. 74; nb. 9; (2004); p.

1376 - 1382, View in Reaxys

E-X, Et-Br

Sagar, Pramod; Froehlich, Roland; Wuerthwein, Ernst-Ulrich; Angewandte Chemie - International Edition; vol. 43; nb. 42; (2004); p. 5694 - 5697, View in Reaxys

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15d

Miyata, Okiko; Koizumi, Tomoko; Asai, Hiroshi; Iba, Ryuichi; Naito, Takeaki; Tetrahedron; vol. 60; nb. 17; (2004); p. 3893 - 3914, View in Reaxys

3d

Ellis, Trevor K.; Martin, Collin H.; Ueki, Hisanori; Soloshonok, Vadim A.; Tetrahedron Letters; vol. 44; nb. 5; (2003); p. 1063 - 1066, View in Reaxys

RBr, R = Et

Zawadzki; Zwierzak; Polish Journal of Chemistry; vol. 77; nb. 3; (2003); p. 315 - 319, View in Reaxys

educt to 4b

Sun, Yong; Ding, Ming-Wu; Heteroatom Chemistry; vol. 14; nb. 4; (2003); p. 348 - 351, View in Reaxys

XVIII

Konevetz; Mironova; Beck; Zenkova; Shishkin; Vlassov; Silnikov; Russian Journal of Bioorganic Chemistry; vol.

28; nb. 4; (2002); p. 331 - 341, View in Reaxys

educt to 3b

Wang, Eng-Chi; Hsu, Ming-Kun; Lin, Yu-Li; Huang, Keng-Shiang; Heterocycles; vol. 57; nb. 11; (2002); p. 1997 2010, View in Reaxys

R1CH2Br, R1=Me

Gardiner, John M; Goss, Andrew D; Majid, Tahir; Morley, Andrew D; Pritchard, Robin G; Warren, John E; Tetrahedron Letters; vol. 43; nb. 43; (2002); p. 7707 - 7710, View in Reaxys

HCHBrMe

Perez, Emma Peralta; Ahrens, Birte; Davidson, Matthew G.; Raithby, Paul R.; Teat, Simon J.; Alvarez, Isidro Perez; Ortiz, Fernando Lopez; Synlett; nb. 2; (2001); p. 275 - 277, View in Reaxys

Ia

Gusarova; Shaikhudinova; Ivanova; Reutskaya; Albanov; Trofimov; Russian Journal of General Chemistry; vol. 71; nb. 5; (2001); p. 718 - 720, View in Reaxys

EtBr, educt to 2

Shigeyasu, Masanori; Kuwahara, Masayasu; Sisido, Masahiko; Ishikawa, Teruhiko; Chemistry Letters; nb. 7; (2001); p. 634 - 635, View in Reaxys

4g

Yakunin; Dyachenko; Litvinov; Chemistry of Heterocyclic Compounds; vol. 37; nb. 6; (2001); p. 766 - 770, View in Reaxys

educt to 3

Abdel Hamid; El-Obeid; Al-Rashood; Khalil; El-Subbagh; Scientia Pharmaceutica; vol. 69; nb. 4; (2001); p. 351 366, View in Reaxys

VIIIc

Beletskaya; Sigeev; Peregudov; Petrovskii; Russian Journal of Organic Chemistry; vol. 37; nb. 10; (2001); p. 1463 1475, View in Reaxys

R-Br to 2

Prajapati; Vora; Pandya; Molecular Crystals and Liquid Crystals Science and Technology Section A: Molecular Crystals and Liquid Crystals; vol. 369; (2001); p. 37 - 46, View in Reaxys

98

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

Table 1/b, Et-Br

Boldrini; Giovenzana; Pagliarin; Palmisano; Sisti; Tetrahedron Letters; vol. 41; nb. 33; (2000); p. 6527 - 6530, View in Reaxys

R'Br, R'=C2H5

Anikin; Krasnova; Kupriyan; Russian Journal of Applied Chemistry; vol. 73; nb. 3; (2000); p. 486 - 489, View in Reaxys

educt to II

Botbaeva; Praliev; Poplavskaya; Nauyryzova; Russian Journal of Organic Chemistry; vol. 36; nb. 10; (2000); p. 1509 - 1513, View in Reaxys

8b

Yakunin; Dyachenko; Litvinov; Chemistry of Heterocyclic Compounds; vol. 36; nb. 12; (2000); p. 1431 - 1436, View in Reaxys

2g

Orita, Akihiro; Watanabe, Akihiro; Tsuchiya, Hiroshi; Otera, Junzo; Tetrahedron; vol. 55; nb. 10; (1999); p. 2889 2898, View in Reaxys

RCH2Br, Tab 1, run 5

Ma, Chunrong; He, Xiaohui; Liu, Xiaoxiang; Yu, Shu; Zhao, Shuo; Cook, James M.; Tetrahedron Letters; vol. 40; nb. 15; (1999); p. 2917 - 2918, View in Reaxys

Table 1, entry 1

Srivastava, Sanjay K.; Chauhan, Prem Man Singh; Bhaduri, Amiya P.; Synthetic Communications; vol. 29; nb. 12; (1999); p. 2085 - 2091, View in Reaxys

25

Ouvrard, Carole; Berthelot, Michel; Laurence, Christian; Journal of the Chemical Society. Perkin Transactions 2; nb. 7; (1999); p. 1357 - 1362, View in Reaxys

R'Br, R'=Et

Mijin; Stojanovic; Petrovic; Russian Journal of Organic Chemistry; vol. 34; nb. 10; (1998); p. 1513 - 1514, View in Reaxys

BrCH2CH3

Banks, William R.; Moerlein, Stephen M.; Parkinson, David; Welch, Michael J.; Medicinal Chemistry Research; vol. 5; nb. 2/3; (1995); p. 150 - 173, View in Reaxys

Patent-Specific Data (52) Prophetic ComLocation in Patent pound

References Patent; The United States of America as Represented by the Secretary of the Navy; StengerSmith, John D; Goodman, Paul A.; (5 pag.); US9862694; (2018); (B1) English, View in Reaxys

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Patent; L'OREAL; DALKO, Maria; HITCE, Julien; (65 pag.); WO2017/29274; (2017); (A1) English, View in Reaxys Patent; SYNGENTA CROP PROTECTION AG; SYNGENTA (CHINA) INVESTMENT CO., LTD.; EDMUNDS, Andrew; HALL, Roger Graham; MUEHLEBACH, Michel; EMERY, Daniel; JUNG, Pierre Joseph Marcel; LU, Long; WU, Yaming; CHEN, Ruifang; (156 pag.); WO2016/169886; (2016); (A1) English, View in Reaxys Patent; Hunan University; HU, AI XI; LI, WAN; DING, NA; YE, JIAO; (13 pag.); CN104327056; (2016); (B) Chinese, View in Reaxys Patent; SUMITOMO CHEMICAL COMPANY, LIMITED; SHIODA, Takayuki; ARIMORI, Sadayuki; (149 pag.); US2016/159755; (2016); (A1) English, View in Reaxys Page/Page column

Patent; ExxonMobil Chemical Patents Inc.; Voskoboynikov, Alexander Z.; Nikulin, Mikhail V.; Tsarev, Alexey A.; Asachenko, Andrey F.; Babkin, Alexander V.; Giesbrecht, Garth Ronald; Canich, Jo Ann Marie; EP2368896; (2011); (A1) English, View in Reaxys; Patent; BOEHRINGER INGELHEIM INTERNATIONAL GMBH; Anderskewitz, Ralf; Martyres, Domnic; Oost, Thorsten; Rist, Wolfgang; Seither, Peter; US2013/23576; (2013); (A1) English, View in Reaxys; Patent; GENENTECH, INC.; Crawford, James John; Ortwine, Daniel Fred; Wei, BinQing; Young, Wendy B.; US2013/116246; (2013); (A1) English, View in Reaxys; Patent; FLECK, Martin; NOSSE, Bernd; HEINE, Niklas; ROTH, Gerald Juergen; US2013/158004; (2013); (A1) English, View in Reaxys; Patent; SU ZHOU JING HONG BIOTECH CO., LTD.; CAI, Zhen-Wei; ZHOU, Ding; LIN, Yougang; CHEN, Ping; US2013/158031; (2013); (A1) English, View in Reaxys; Patent; Su, Wei-Guo; Deng, Wei; Li, Jinshui; Ji, Jianguo; US2013/210831; (2013); (A1) English, View in Reaxys; Patent; The United States of America as represented by the Secretary of the Air Force; Tan, Loon-Seng; Kannan, Ramamurthi; Dalton, Matthew; US8580958; (2013); (B1) English, View in Reaxys; Patent; NERVIANO MEDICAL SCIENCES S.R.L.; Caldarelli, Marina; Casuscelli, Francesco; Donati, Daniele; Mirizzi, Danilo; Quartieri, Francesca; Silvagni, Marco; US2013/302416; (2013); (A1) English, View in Reaxys; Patent; Huazhong University of Science and Technology; Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.; JIANG, Fengchao; ZHOU, Ping; CHEN, Jianguo; WANG, Yue; CAO, Baoshuai; YAN, Jia; EP2682390; (2014); (A1) English, View in Reaxys; Patent; Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd.; Huazhong University of Science and Technology; JIANG, Fengchao; ZHOU, Ping; CHEN, Jianguo; WANG, Yue; CAO, Baoshuai; YAN, Jia; US2014/4155; (2014); (A1) English, View in Reaxys; Patent; KEMPHYS LTD.; RESEARCH FOUNDATION ITSUU LABORATORY; Muratake, Hideaki; Ito, Ai; Shudo, Koichi; US2014/31575; (2014); (A1) English, View in Reaxys; Patent; HUTCHISON MEDIPHARMA LIMITED; Su, Wei-Guo; Deng, Wei; Ji, Jianguo; US2014/121200; (2014); (A1) English, View in Reaxys; Patent; Sun Pharma Advanced Research Company Ltd.; Rathod, Rajendrasinh; Bhatt, Tushar; Joshi, Kritkumar; Dole, Binaka; Murty, Kadiyala V.S.N.; Thennati, Rajamannar; US2014/155596; (2014); (A1) English, View in Reaxys; Patent; ROLIC AG; Lincker, Frederic; Bury S. Pires, Izabela; Chappellet, Sabrina; Scandiucci De Freitas, Patricia; Ibn-Elhaj, Mohammed; Tang, Qian; Palika, Satish; Hoshino, Masato; Eckert, Jean-Francois; US2014/192305; (2014); (A1) English, View in Reaxys; Patent; BOEHRINGER INGELHEIM INTERNATIONAL GMBH; GNAMM, Christian; OOST, Thorsten; PETERS, Stefan; US2014/221335; (2014); (A1) English, View in Reaxys; Patent; BROMINE COMPOUNDS LTD.; BEN-DAVID, Iris; MIASKOVSKI, Gershon; KOMPANIETS, Igor; US2014/262818; (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; Janssen Pharmaceutica NV; Sui, Zhihua; Subasinghe, Nalin; US2014/275172; (2014); (A1) English, View in Reaxys; Patent; INTERNATIONAL FLAVORS and FRAGRANCES INC.; Closson, Adam P.; Oesterle, Ryan D.; Giffin, Nicole L.; Monteleone, Michael G.; EP2801571; (2014); (A1) English, View in Reaxys; Patent; MSN Laboratories Limited; Reddy, Manne Satyanarayana; Rajan, Srinivasan Thirumalai; Eswaraiah, Sajja; Vishnuvardhan, Sunkara; US2014/343285; (2014); (A1) English, View in Reaxys; Patent; Warner Babcock Institute For Green Chemistry, LLC; Warner, John C.; Gladding, Jeffery A.; Gero, Thomas W.; Cheruku, Srinivasa R.; US2015/65510; (2015); (A1) English, View in Reaxys; Patent; Albrecht, Brian K.; Bellon, Steven F.; Gehling, Victor S.; Harmange, Jean-Christophe; LeBlanc, Yves; Liang, Jun; Magnuson, Steven; Tsui, Vicki; Zhang, Birong; US2015/65522; (2015); (A1) English, View in Reaxys; Patent; Life Technologies Corporation; Kang, Hee Chol; Gee, Kyle; Johnson, Iain; Janes, Michael; US8981100; (2015); (B2) English, View in Reaxys; Patent; SUNSHINE LAKE PHARMA CO., LTD.; Zhang, Yingjun; Zhang, Jiancun; Wang, Xiaojun; Lin, Runfeng; Cao, Shengtian; Wang, Zhaohe; Li, Jing; US2015/87639; (2015); (A1) English, View in Reaxys; Patent; Kozelj, Matjaz; Guerfi, Abdelbast; Trottier, Julie; Zaghib, Karim; US2015/93655; (2015); (A1) English, View in Reaxys; Patent; YANG, Qiang; LORSBACH, Beth; WHITEKER, Gregory T.; ROTH, Gary; DeAMICIS, Carl; CLARK, Thomas P.; GRAY, Kaitlyn; CANTURK, Belgin; KANE, Elisabeth J.; ZHANG, Yu; MUHUHI, Joseck M.; US2015/112076; (2015); (A1) English, View in Reaxys; Patent; YANG, Qiang; LORSBACH, Beth; WHITEKER, Gregory T.; ROTH, Gary; DeAMI-

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CIS, Carl; CLARK, Thomas; GRAY, Kaitlyn; ZHANG, Yu; MUHUHI, Joseck M.; US2015/112074; (2015); (A1) English, View in Reaxys; Patent; YANG, Qiang; LORSBACH, Beth; ROTH, Gary; NIYAZ, Noormohamed M.; NISSEN, Jeffrey; ROSS, JR., Ronald; WHITEKER, Gregory T.; DeAMICIS, Carl; GRAY, Kaitlyn; ZHANG, Yu; US2015/112077; (2015); (A1) English, View in Reaxys; Patent; Hoffmann-La Roche Inc.; Feng, Song; Gao, Lu; Hong, Di; Wang, Lisha; Yun, Hongying; Zhao, Shu-Hai; US2015/158879; (2015); (A1) English, View in Reaxys; Patent; Glaxo Group Limited a corporation; Atkinson, Stephen John; Barker, Michael David; Campbell, Matthew; Diallo, Hawa; Douault, Clement; Garton, Neil Stuart; Liddle, John; Sheppard, Robert John; Walker, Ann Louise; Wellaway, Christopher; Wilson, David Matthew; US2015/175600; (2015); (A1) English, View in Reaxys; Patent; Dow AgroSciences LLC; Li, Xiaoyong; Yang, Qiang; Lorsbach, Beth; US9085552; (2015); (B1) English, View in Reaxys; Patent; HOFFMANN-LA ROCHE INC.; Han, Xingchun; Javanbakht, Hassan; Jiang, Min; Liang, Chungen; Wang, Jianping; Wang, Yongguang; Wang, Zhanguo; Weikert, Robert James; Yang, Song; Zhou, Chengang; US2015/210682; (2015); (A1) English, View in Reaxys Patent; BOEHRINGER INGELHEIM INTERNATIONAL GMBH; KLEY, Joerg; FRATTINI, Sara; HAMPRECHT, Dieter; HECKEL, Armin; US2015/18313; (2015); (A1) English, View in Reaxys Page/Page column

Patent; YANG, Qiang; LORSBACH, Beth; WHITEKER, Gregory T.; DeAMICIS, Carl; MUHUHI, Joseck M.; US2015/111938; (2015); (A1) English, View in Reaxys Patent; Shanghai Jingxin Biomedical Co., Ltd.; Shangyu Jingxin Pharmaceutical Co., Ltd.; Huang, Yue; ZHENG, Fei; US2015/225348; (2015); (A1) English, View in Reaxys Patent; Osaka Organic Chemical IndustryCo., Ltd.; Tanaka, Shinji; Kono, Naoya; (14 pag.); JP2015/107923; (2015); (A) Japanese, View in Reaxys Patent; Technion Research and Development Foundation Limited; Ein-Eli, Yair; Luder, Daniel; Kraytsberg, Alexander; US2014/142332; (2014); (A1) English, View in Reaxys Patent; ORION CORPORATION; WOHLFAHRT, Gerd; RUMMAKKO, Petteri; KARJALAINEN, Arja; PASSINIEMI, Mikko; PIETIKÄINEN, Pekka; HAIKARAINEN, Anssi; VÄISÄNEN, Emilia; TIAINEN, Eija; WO2014/202827; (2014); (A1) English, View in Reaxys Patent; SAUDI BASIC INDUSTRIES CORPORATION; SABIC PETROCHEMICAL B.V.; SAINANI, Jaiprakash Brijlal; DAVADRA, Mahesh; WO2013/29767; (2013); (A1) English, View in Reaxys Patent; TELIGENE LTD.; ZHANG, Dawei; WO2013/41038; (2013); (A1) English, View in Reaxys Patent; BASF SE; Pichlmair, Stefan; Schmidt-Leithoff, Joachim; US2013/109876; (2013); (A1) English, View in Reaxys

Claim

Patent; Bonrath, Werner; Pace, Francesco; Fischesser, Jocelyn; Witzgall, Konrad; US2012/197046; (2012); (A1) English, View in Reaxys; Patent; JSC GRINDEKS; US2012/220656; (2012); (A1) English, View in Reaxys Patent; JNC Corporation; JNC Petrochemical Corporation; EP2484658; (2012); (A1) English, View in Reaxys Patent; LG LIFE SCIENCES LTD.; SONG, Jeong Uk; KIM, Geun Tae; CHOI, Sung Pil; JUNG, Cheol Kyu; PARK, Deok Seong; CHOI, Eun Sil; KIM, Tae Hun; PARK, Hyun Jung; PARK, Wan Su; PARK, Heui Sul; KOO, Ki Chul; ARTEMOV, Vasily; WO2011/43568; (2011); (A2) English, View in Reaxys Patent; ANACOR PHARMACEUTICALS, INC.; ZHOU, Huchen; DING, Dazhong; SUN, Daoan; ZHOU, Yasheen; ZHANG, Yong-kang; PLATTNER, Jacob, J.; WO2011/49971; (2011); (A1) English, View in Reaxys Patent; VERTEX PHARMACEUTICALS INCORPORATED; ARONOV, Alex; COME, Jon, H.; DAVIES, Robert, J.; PIERCE, Albert, C.; WANG, Jian; NANTHAKUMAR, Suganthini; CAO, Jingrong; BANDARAGE, Upul, K.; KRUEGER, Elaine; TIRAN, Amaud, Le; LIAO, Yusheng; MESSERSMITH, David; COLLIER, Philip, N.; GREY, Ronald; O'DOWD, Hardwin; HENDERSON, James, A.; GRILLOT, Anne-Laure; WO2011/87776; (2011); (A1) English, View in Reaxys Patent; SANOFI; US2011/312972; (2011); (A1) English, View in Reaxys Patent; Iwata, Hidehisa; Kohara, Yasuhisa; Cao, Sheldon X.; Guntupalli, Prasuna; Gwaltney, Stephen L.; Hosfield, David J.; Liu, Yan; Stafford, Jeffrey A.; Throop, Beverly; US2010/69431; (2010); (A1) English, View in Reaxys

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Claim

Patent; Tosoh Corporation; EP271212; (1988); (A2) English, View in Reaxys; Patent; Innothera; US4079140; (1978); (A) English, View in Reaxys; Patent; Wischnat, Ralf; Rudolph, Joachim; US2004/19219; (2004); (A1) English, View in Reaxys Patent; Sato, Nagaaki; Ando, Makoto; Ishikawa, Shiho; Nagase, Tsuyoshi; Nagai, Keita; Kanatani, Akio; US2004/72874; (2004); (A1) English, View in Reaxys Patent; Goedecke GmbH; US6740768; (2004); (B1) English, View in Reaxys Patent; BAYER HEALTHCARE AG; WO2004/52852; (2004); (A1) German, View in Reaxys Patent; Prudhomme, Michelle; Marminon, Christelle; Routier, Sylvain; Coudert, Gerard; Merour, Jean-Yves; Hickman, John; Pierre, Alain; Renard, Pierre; Pfeiffer, Bruno; US2004/152721; (2004); (A1) English, View in Reaxys Patent; Perez, Michel; Lamothe, Marie; Hill, Bridget; Etievant, Chantal; US2004/204417; (2004); (A1) English, View in Reaxys Patent; MITSUBISHI GAS CHEMICAL COMPANY, INC.; EP1468981; (2004); (A1) English, View in Reaxys Patent; Basilea Pharmaceutica AG; US6821980; (2004); (B1) English, View in Reaxys Patent; Solvent Innovation GmbH; EP1182197; (2002); (A1) German, View in Reaxys Patent; Mitsubishi Pharma Corporation; EP1195372; (2002); (A1) English, View in Reaxys Patent; Advanced Medicine, Inc.; US6337423; (2002); (B1) English, View in Reaxys Patent; Lonza AG; US6350898; (2002); (B1) English, View in Reaxys Patent; Zambon Group S.p.A.; US6358973; (2002); (B1) English, View in Reaxys

prophetic product

Patent; Eastman Chemical Company; US6355837; (2002); (B1) English, View in Reaxys; Patent; Bayer Aktiengesellschaft; US3957779; (1976); (A) English, View in Reaxys; Patent; Sanraku-Ocean Co., Ltd.; US4368203; (1983); (A) English, View in Reaxys; Patent; Sumitomo Chemical Company, Limited; US4055565; (1977); (A) English, View in Reaxys; Patent; Rhone-Poulenc Chimie; US5777151; (1998); (A) English, View in Reaxys; Patent; Sumitomo Chemical Company, Limited; US6034128; (2000); (A) English, View in Reaxys

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prophetic product

Patent; Kureha Kagaku Kogyo Kabushiki Kaisha; US6339045; (2002); (B1) English, View in Reaxys Patent; Pharmacia and Upjohn Company; US6342513; (2002); (B1) English, View in Reaxys

prophetic product

Patent; Sumitomo Chemical Company, Limited; EP1172356; (2002); (A1) English, View in Reaxys

Druglikeness (1) 1 of 1

LogP

1.736

H Bond Donors

0

H Bond Acceptors

0

Rotatable Bonds

0

TPSA

0

Lipinski Number

4

Veber Number

2

Derivative (10) Comment (Derivative)

References

CT-Komplex mit IOD:UV;IP

Strong; Kaye; Journal of the American Chemical Society; vol. 98; (1976); p. 5460,5461, View in Reaxys

Komplex mit IAtom: UV (S. 717)

Brosseau et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 716, View in Reaxys

Komplex mit BrAtom: UV (S. 717)

Brosseau et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 716, View in Reaxys

EtBr*AlBr3: ohne Angabe

Kinsella,E.; Coward,J.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p.

2139 - 2143, View in Reaxys

Komplex m.

C10H8 : Abs.bande

Bolotnikova; Sichkar; Journal of Applied Spectroscopy; vol. 9; (1965); p. 1003; ; p. 500, View in Reaxys

Additionsverbindung mit AlBr3

Perkampus; Baumgarten; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 496, View in Reaxys

Additionsverbindung mit GaBr3

Perkampus; Baumgarten; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 496, View in Reaxys

Komplex mit MeOH(1:4)

Bardamowa; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk; vol. 2; (1960); p.

71,73, View in Reaxys

compound with wa- v.Stackelberg; Mueller; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 58; (1954); p. ter; Further Data 25,26, View in Reaxys see Handbook hydrate; Further Data see Handbook (Preparation)

Villard; Annales de Chimie (Cachan, France); vol. <7>11; (1897); p. 377, View in Reaxys

Purification (1) References Krasil'nikova et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 2489,2275,2276,2277, View in Reaxys Melting Point (11) 1 of 11

Melting Point [°C]

72 - 74

Location

supporting information

McKeever, Caitriona; Kaiser, Marcel; Rozas, Isabel; Journal of Medicinal Chemistry; vol. 56; nb. 3; (2013); p. 700 - 711, View in Reaxys 2 of 11

Comment (Melting Point)

Decomp.at:13 degreeC.bei 760 Torr.

v.Stackelberg; Mueller; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 58; (1954); p. 25,26, View in Reaxys 3 of 11

Melting Point [°C]

-118.6

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2018-07-24 18:37:32

Timmermans; Bulletin des Societes Chimiques Belges; vol. 61; (1952); p. 393,396, View in Reaxys 4 of 11

Melting Point [°C]

-118.5

Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys 5 of 11

Melting Point [°C]

-70 - 80

Comment (Melting Point)

unter Drucken 5000 und 30000 kg/cmE2.

Bridgman; Journal of Chemical Physics; vol. 9; (1941); p. 797; Pr.am.Acad.Arts Sci.; vol. 77; p. 142; Chem.Abstr.; (1949); p.

4067, View in Reaxys 6 of 11

Melting Point [°C]

-118.9

Skau; McCullough; Journal of the American Chemical Society; vol. 57; (1935); p. 2440, View in Reaxys 7 of 11

Melting Point [°C]

-119

Timmermans; Chem. Zentralbl.; vol. 82; nb. II; (1911); p. 1015, View in Reaxys; Timmermans; Bulletin des Societes Chimiques Belges; vol. 32; (1923); p. 300; Chem. Zentralbl.; vol. 94; nb. III; (1923); p. 1497, View in Reaxys; Timmermans; Bulletin des Societes Chimiques Belges; vol. 37; (1928); p. 412; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 522, View in Reaxys 8 of 11

Melting Point [°C]

-115.5

Wroczynski; Guye; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 8; (1910); p. 197, View in Reaxys 9 of 11

Melting Point [°C]

-117.8

Guttmann; Journal of the Chemical Society; vol. 87; (1905); p. 1040, View in Reaxys 10 of 11

Melting Point [°C]

-115.8

Ladenburg; Kruegel; Chemische Berichte; vol. 33; (1900); p. 638; Chemische Berichte; vol. 32; (1899); p. 1821, View in Reaxys 11 of 11

Melting Point [°C]

-125.5

Schneider; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 22; (1897); p. 233, View in Reaxys Boiling Point (25) Boiling Point [°C]

Pressure (Boiling Point) [Torr]

38

40

Location

References

supporting informa- Choquette, Kimberly A.; Sadasivam, Dhandapani V.; Flowers, Robert tion A.; Journal of the American Chemical Society; vol. 132; nb. 49; (2010); p.

17396 - 17398, View in Reaxys 75.006

Vugts, Danielle J.; Koningstein, Manoe M.; Schmitz, Rob F.; De Kanter, Frans J. J.; Groen, Marinus B.; Orru, Romano V. A.; Chemistry - A European Journal; vol. 12; nb. 27; (2006); p. 7178 - 7189, View in Reaxys

40

Boyd; Meadow; Analytical Chemistry; vol. 32; (1960); p. 551,552, View in Reaxys; Patent; Hassan, Jomaa; US6680308; (2004); (B1) English, View in Reaxys

38 - 39

Kurihara,Y. et al.; Bulletin of the Chemical Society of Japan; vol. 38; (1965); p. 29 - 32, View in Reaxys; Sinyashin, O.G.; Karimullin, Sh. A.; Kostin, V. P.; Batyeva, E. S.; Pudovik, A. N.; J. Gen. Chem. USSR (Engl.

Transl.); vol. 56; nb. 8; (1986); p. 1700 - 1707,1505 - 1511, View in Reaxys; Baklan, V. F.; Khil'chevskii, A. N.; D'yakovskaya, V. M.; Sologub, L. S.; Kukhar, V. P.; Russian Journal of Organic Chemistry; vol. 29; nb. 3.1; (1993); p. 454 - 456; Zhurnal Organicheskoi Khimii; vol. 29; nb. 3; (1993); p. 542 - 545, View in Reaxys; Yang; Lin; Li; Synthetic Communications; vol. 31; nb. 18; (2001); p. 2817 - 2822, View in Reaxys

38 - 40

Gatilov,Yu.F.; Perov,V.A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 106 - 109,87 - 90, View in Reaxys; Gazizov, T. Kh.; Sudarev, Yu. I.; Shakirov, I. Kh.; Smirnov, V. N.; Pudovik, A. N.; J. Gen. Chem.

USSR (Engl. Transl.); vol. 52; nb. 4; (1982); p. 769 - 776,667 - 673, View in Reaxys

38.4

Wagner,B.O.; Hammond,G.S.; Journal of Organometallic Chemistry; vol.

85; (1975); p. 1 - 14, View in Reaxys; Krasil'nikova et al.; J. Gen. Chem.

USSR (Engl. Transl.); vol. 47; (1977); p. 2489,2275,2276,2277, View in Reaxys

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38.38

760

Svoboda et al.; Collection of Czechoslovak Chemical Communications; vol. 42; (1977); p. 1755,1756,1757,1759, View in Reaxys

38

Heel; Zeil; Zeitschrift fuer Elektrochemie; vol. 64; (1960); p. 962,963-971; Chem.Abstr.; vol. 55; nb. 115; (1961), View in Reaxys; Kier; Hall; Journal of Pharmaceutical Sciences; vol. 65; (1976); p. 1806,1808, View in Reaxys; Murai; Kimura; Nippon Kagaku Zasshi; vol. 90; (1969); p. 503, View in Reaxys

72

Guibe; Sarthou; Bram; Tetrahedron; vol. 30; nb. 17; (1974); p. 3139 3151, View in Reaxys

36 - 37

Zwierzak et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 22; (1974); p. 673, View in Reaxys

36.5 - 37

Schrumpf; Klein; Chemische Berichte; vol. 106; (1973); p. 266,278, View in Reaxys

39

Murai; Kimura; Nippon Kagaku Kaishi; (1972); p. 2096,2097, View in Reaxys; Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys

38.5 - 40

Anderson Jr.; Freenor; Journal of Organic Chemistry; vol. 37; (1972); p.

626, View in Reaxys

34.2

680

38 - 38.5

Kairatis; Stimson; Australian Journal of Chemistry; vol. 24; (1971); p.

2031,2033, View in Reaxys Hudson; Loveday; Journal of the Chemical Society [Section] B: Physical Organic; (1966); p. 766,768, View in Reaxys

38

750

Barker; Maccoll; Journal of the Chemical Society; (1963); p. 2839, View in Reaxys

38.4

763

Melendez-Andreu; Annales de Chimie (Cachan, France); vol. 7; nb. 13; (1962); p. 695,702, View in Reaxys

38.2

760

Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys

48 - 226

1125.3 - 36701.8

Tarassenkow; Afinogenow; Zhurnal Fizicheskoi Khimii; vol. 9; (1937); p.

889,896; Chem. Zentralbl.; vol. 109; nb. I; (1938); p. 4295, View in Reaxys

38.34

760

Skau; McCullough; Journal of the American Chemical Society; vol. 57; (1935); p. 2440, View in Reaxys

28.14 - 75.37

525.8 - 2347.4

Zmaczynski; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 27; (1930); p. 514; Chem. Zentralbl.; vol. 102; nb. I; (1931); p.

1319, View in Reaxys; Zmaczynski; Roczniki Chemii; vol. 13; p. 181; Chem. Zentralbl.; vol. 104; nb. II; (1933); p. 515, View in Reaxys

28.13 - 75.48

525.8 - 2347.4

Zmaczynski; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 27; (1930); p. 514; Chem. Zentralbl.; vol. 102; nb. I; (1931); p.

1319, View in Reaxys; Zmaczynski; Roczniki Chemii; vol. 13; p. 181; Chem. Zentralbl.; vol. 104; nb. II; (1933); p. 515, View in Reaxys

38.4

760

Grimm; Patrick; Journal of the American Chemical Society; vol. 45; (1923); p. 2799, View in Reaxys; Timmermans; Chem. Zentralbl.; vol. 82; nb. II; (1911); p. 1015, View in Reaxys; Tyrer; Journal of the Chemical Society; vol. 105; (1914); p. 2538, View in Reaxys; Timmermans; Bulletin des Societes Chimiques Belges; vol. 32; (1923); p. 300; Chem. Zentralbl.; vol. 94; nb. III; (1923); p. 1497, View in Reaxys; Zmaczynski; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 27; (1930); p. 514; Chem. Zentralbl.; vol. 102; nb. I; (1931); p. 1319, View in Reaxys; Zmaczynski; IX.Congr.int.Quim.pura apl.<Madrid 1934>Bd.2,S.230, View in Reaxys

38.3

760

Roland; Bulletin des Societes Chimiques Belges; vol. 37; (1928); p. 122; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 2900, View in Reaxys

38.37

Regnault; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1863); p. 70, View in Reaxys

Refractive Index (41)

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Refractive Index

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

References

1.42052

589

25

Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 7; (1994); p. 703 - 708, View in Reaxys; Arial, Manuela; Embid, Jose Munoz; Otin, Santos; Velasco, Inmaculada; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 100; nb. 10; (1996); p. 1752 - 1758, View in Reaxys

1.42052

589

298.2

Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 6; (1994); p. 609 - 616, View in Reaxys

1.4231

589

20

Baklan, V. F.; Khil'chevskii, A. N.; D'yakovskaya, V. M.; Sologub, L. S.; Kukhar, V. P.; Russian Journal of Organic Chemistry; vol. 29; nb. 3.1; (1993); p. 454 - 456; Zhurnal Organicheskoi Khimii; vol. 29; nb. 3; (1993); p. 542 - 545, View in Reaxys

1.426

589

20

Sinyashin, O.G.; Karimullin, Sh. A.; Kostin, V. P.; Batyeva, E. S.; Pudovik, A. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 56; nb. 8; (1986); p.

1700 - 1707,1505 - 1511, View in Reaxys

1.4217

632.8

20

Vul'fson, S.G.; Dianova, O.M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; nb. 10; (1984); p. 2070 - 2074; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 10; (1984); p. 2269 - 2274, View in Reaxys

1.431

589

18

Sinyashin, O. G.; Karimullin, Sh. A.; Pudovik, D. A.; Batyeva, E. S.; Pudovik, A. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 54; nb. 11; (1984); p. 2458 - 2463,2195 - 2199, View in Reaxys

1.422

589

20

Gazizov, T. Kh.; Sudarev, Yu. I.; Shakirov, I. Kh.; Smirnov, V. N.; Pudovik, A. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 52; nb. 4; (1982); p.

769 - 776,667 - 673, View in Reaxys

1.42464

589.3

20

Chen, C. C.; Vedam, K.; Journal of Chemical Physics; vol. 73; nb. 9; (1980); p. 4577 - 4584, View in Reaxys

1.4269

546.1

20

Chen, C. C.; Vedam, K.; Journal of Chemical Physics; vol. 73; nb. 9; (1980); p. 4577 - 4584, View in Reaxys

1.4251

589

20

Gatilov,Yu.F.; Perov,V.A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 106 - 109,87 - 90, View in Reaxys

1.4241

589

20

Svoboda et al.; Collection of Czechoslovak Chemical Communications; vol. 42; (1977); p. 1755,1756,1757,1759, View in Reaxys

1.425

589

1.423

589

20

Zwierzak et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 22; (1974); p. 673, View in Reaxys

1.424

589

20

Melendez-Andreu; Annales de Chimie (Cachan, France); vol. 7; nb. 13; (1962); p. 695,702, View in Reaxys; Kairatis; Stimson; Australian Journal of Chemistry; vol. 24; (1971); p. 2031,2033, View in Reaxys

1.4244

589

20

Cowley; Partington; Journal of the Chemical Society; (1937); p. 130,131, View in Reaxys; Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys

1.4212

589

25

Barker; Maccoll; Journal of the Chemical Society; (1963); p. 2839, View in Reaxys

1.4246

589

20

Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p.

857, View in Reaxys; Heel; Zeil; Zeitschrift fuer Elektrochemie; vol. 64; (1960); p. 962,963-971; Chem.Abstr.; vol. 55; nb. 115; (1961), View in Reaxys

1.42104

589

25

Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p.

207, View in Reaxys

1.42416

589

20

Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p.

207, View in Reaxys

1.4211

589

25

Fleming; Saunders; Journal of the Chemical Society; (1955); p. 4147,4148, View in Reaxys

Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p. 673,678, View in Reaxys

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1.4276

589

15.1

Fleming; Saunders; Journal of the Chemical Society; (1955); p. 4147,4148, View in Reaxys

1.459

589

20

Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p. 330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys

1.41636

589

25

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p.

2071,2072, View in Reaxys

1.4242

589

20

Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys

1.422

656.3

20

Vogel; Journal of the Chemical Society; (1943); p. 643, View in Reaxys

1.4247

589

20

Vogel; Journal of the Chemical Society; (1943); p. 643, View in Reaxys

1.4314

486.1

20

Vogel; Journal of the Chemical Society; (1943); p. 643, View in Reaxys

1.4364

434

20

Vogel; Journal of the Chemical Society; (1943); p. 643, View in Reaxys

1.4608 - 1.4303

589

-40 - 10

Grosse; Wackher; Linn; Journal of Physical Chemistry; vol. 44; (1940); p.

293, View in Reaxys

1.42405

589

26

Smyth; Engel; Journal of the American Chemical Society; vol. 51; (1929); p. 2649, View in Reaxys

1.4247

656.3

15

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.42756

589

15

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.4342

486.1

15

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.43976

434

15

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

1.41556

589

32.1

Schwers; Bl.Acad.Belg.; (1912); p. 621, View in Reaxys

1.42577

589

16

Schwers; Bl.Acad.Belg.; (1912); p. 621, View in Reaxys

1.4254

589

15

Beythien; Hennicke; P.C.H.; vol. 48; (1907); p. 1006, View in Reaxys

1.432

589

8

Gladstone; Journal of the Chemical Society; vol. 59; (1891); p. 293, View in Reaxys

1.42113

656.3

20

Weegmann; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 2; (1888); p. 236, View in Reaxys

1.42386

589

20

Weegmann; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 2; (1888); p. 236, View in Reaxys

1.43595

434

20

Weegmann; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 2; (1888); p. 236, View in Reaxys

Density (42) 1 of 42

Density [g·cm-3]

1.45038

Measurement Temperature 25 [°C] Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 6; (1994); p. 609 - 616, View in Reaxys; Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 7; (1994); p. 703 - 708, View in Reaxys; Arial, Manuela; Embid, Jose Munoz; Otin, Santos; Velasco, Inmaculada; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 100; nb. 10; (1996); p. 1752 - 1758, View in Reaxys 2 of 42

Density [g·cm-3]

1.2335 - 1.4627

Measurement Temperature 20 - 120 [°C] Rutherford, W. M.; Journal of Chemical & Engineering Data; vol. 33; nb. 3; (1988); p. 234 - 237, View in Reaxys 3 of 42

Density [g·cm-3]

1.4555

Reference Temperature [°C]

4

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Measurement Temperature 20 [°C] Weegmann; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 2; (1888); p. 236, View in Reaxys; Vul'fson, S.G.; Dianova, O.M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; nb. 10; (1984); p. 2070 - 2074; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb.

10; (1984); p. 2269 - 2274, View in Reaxys 4 of 42

Density [g·cm-3]

1.4545

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Gazizov, T. Kh.; Sudarev, Yu. I.; Shakirov, I. Kh.; Smirnov, V. N.; Pudovik, A. N.; J. Gen. Chem. USSR (Engl. Transl.); vol.

52; nb. 4; (1982); p. 769 - 776,667 - 673, View in Reaxys 5 of 42

Density [g·cm-3]

1.4646

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Holm, Torkil; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1981); p. 464 - 467, View in Reaxys 6 of 42

Density [g·cm-3]

1.45148

Reference Temperature [°C]

4

Measurement Temperature 25 [°C] Svoboda et al.; Collection of Czechoslovak Chemical Communications; vol. 42; (1977); p. 1755,1756,1757,1759, View in Reaxys 7 of 42

Density [g·cm-3]

3

Measurement Temperature 20 [°C] Bytenskii; J. Appl. Chem. USSR (Engl. Transl.); vol. 45; (1972); p. 453,458, View in Reaxys 8 of 42

Density [g·cm-3]

1.461

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Melendez-Andreu; Annales de Chimie (Cachan, France); vol. 7; nb. 13; (1962); p. 695,702, View in Reaxys 9 of 42

Gorenbein; Smolenzew; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 28; (1962); p. 185, View in Reaxys

10 of 42

Density [g·cm-3]

1.44917

Reference Temperature [°C]

4

Measurement Temperature 25 [°C] Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p. 207, View in Reaxys 11 of 42

Density [g·cm-3]

1.45939

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p. 207, View in Reaxys

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12 of 42

Density [g·cm-3]

1.4704

Reference Temperature [°C]

4

Measurement Temperature 15.1 [°C] Fleming; Saunders; Journal of the Chemical Society; (1955); p. 4147,4148, View in Reaxys 13 of 42

Density [g·cm-3]

1.449

Reference Temperature [°C]

4

Measurement Temperature 25 [°C] Fleming; Saunders; Journal of the Chemical Society; (1955); p. 4147,4148, View in Reaxys 14 of 42

Density [g·cm-3]

1.4612

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys 15 of 42

Density [g·cm-3]

1.4515

Reference Temperature [°C]

4

Measurement Temperature 25 [°C] Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys 16 of 42

Density [g·cm-3]

1.4676

Reference Temperature [°C]

4

Measurement Temperature 17.5 [°C] Vogel; Journal of the Chemical Society; (1943); p. 643, View in Reaxys 17 of 42

Density [g·cm-3]

1.4604

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Vogel; Journal of the Chemical Society; (1943); p. 643, View in Reaxys 18 of 42

Density [g·cm-3]

1.4613

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Sepalowa-Michailowa; Trudy Inst.c.chim.Reakt.; vol. 16; (1939); p. 71; Chem.Abstr.; (1940); p. 3960, View in Reaxys 19 of 42

Density [g·cm-3]

1.4512

Reference Temperature [°C]

4

Measurement Temperature 25 [°C] Skau; McCullough; Journal of the American Chemical Society; vol. 57; (1935); p. 2440, View in Reaxys 20 of 42

Density [g·cm-3]

1.4164 - 1.695

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Reference Temperature [°C]

4

Measurement Temperature -100 - 40 [°C] Morgan; Lowry; Journal of Physical Chemistry; vol. 34; (1930); p. 2411, View in Reaxys 21 of 42

Density [g·cm-3]

1.4586

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Smyth; Morgan; Journal of the American Chemical Society; vol. 50; (1928); p. 1554, View in Reaxys; Smyth; Engel; Journal of the American Chemical Society; vol. 51; (1929); p. 2649, View in Reaxys 22 of 42

Density [g·cm-3]

1.4245 - 1.6737

Reference Temperature [°C]

4

Measurement Temperature -89.2 - 36.6 [°C] Smyth; Morgan; Journal of the American Chemical Society; vol. 50; (1928); p. 1554, View in Reaxys 23 of 42

Density [g·cm-3]

1.50136

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys 24 of 42

Density [g·cm-3]

1.4708

Reference Temperature [°C]

4

Measurement Temperature 151 [°C] Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys 25 of 42

Density [g·cm-3]

1.4403

Reference Temperature [°C]

4

Measurement Temperature 30 [°C] Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys 26 of 42

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Timmermans; Bulletin des Societes Chimiques Belges; vol. 32; (1923); p. 300; Chem. Zentralbl.; vol. 94; nb. III; (1923); p.

1497, View in Reaxys 27 of 42

Density [g·cm-3]

1.49821

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Tyrer; Journal of the Chemical Society; vol. 105; (1914); p. 2538, View in Reaxys 28 of 42

Measurement Temperature 0 [°C]

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Tyrer; Journal of the Chemical Society; vol. 105; (1914); p. 2538, View in Reaxys; Timmermans; Bulletin des Societes Chimiques Belges; vol. 20; (1906); p. 400, View in Reaxys 29 of 42

Measurement Temperature 32 [°C] Tyrer; Journal of the Chemical Society; vol. 105; (1914); p. 2538, View in Reaxys

30 of 42

Density [g·cm-3]

1.4973

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Koerber; Chem. Zentralbl.; vol. 83; nb. I; (1912); p. 1274, View in Reaxys; Koerber; Annalen der Physik (Weinheim, Germany); vol. <4>37; (1912); p. 1021; Chem. Zentralbl.; vol. 83; nb. I; (1912); p. 1274, View in Reaxys 31 of 42

Density [g·cm-3]

1.45543

Reference Temperature [°C]

4

Measurement Temperature 20.9 [°C] Schwers; Bl.Acad.Belg.; (1912); p. 620, View in Reaxys 32 of 42

Density [g·cm-3]

1.44561

Reference Temperature [°C]

4

Measurement Temperature 25.7 [°C] Schwers; Bl.Acad.Belg.; (1912); p. 620, View in Reaxys 33 of 42

Measurement Temperature -120 [°C] Koerber; Annalen der Physik (Weinheim, Germany); vol. <4>37; (1912); p. 1021; Chem. Zentralbl.; vol. 83; nb. I; (1912); p.

1274, View in Reaxys

34 of 42

Measurement Temperature 20 [°C] Koerber; Annalen der Physik (Weinheim, Germany); vol. <4>37; (1912); p. 1021; Chem. Zentralbl.; vol. 83; nb. I; (1912); p.

1274, View in Reaxys

35 of 42

Density [g·cm-3]

1.50138

Reference Temperature [°C]

4

Measurement Temperature 0 [°C] Timmermans; Chem. Zentralbl.; vol. 81; nb. II; (1910); p. 442, View in Reaxys 36 of 42

Density [g·cm-3]

1.45983

Reference Temperature [°C]

4

Measurement Temperature 20 [°C] Patterson; Thomson; Journal of the Chemical Society; vol. 93; (1908); p. 356 Anm., View in Reaxys 37 of 42

Density [g·cm-3]

1.4307

Reference Temperature [°C]

4

Measurement Temperature 20 [°C]

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Richards; Mathews; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 61; (1908); p. 452; Journal of the American Chemical Society; vol. 30; (1908); p. 10, View in Reaxys 38 of 42

Measurement Temperature -77 [°C] Timmermans; Bulletin des Societes Chimiques Belges; vol. 20; (1906); p. 400, View in Reaxys

39 of 42

Density [g·cm-3]

1.487

Measurement Temperature 8 [°C] Gladstone; Journal of the Chemical Society; vol. 59; (1891); p. 293, View in Reaxys 40 of 42

Density [g·cm-3]

1.4134

Reference Temperature [°C]

4

Measurement Temperature 38.4 [°C] Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 563, View in Reaxys 41 of 42

Density [g·cm-3]

1.44988

Reference Temperature [°C]

15

Measurement Temperature 15 [°C] Perkin; Journal fuer Praktische Chemie (Leipzig); vol. <2>31; (1885); p. 500, View in Reaxys 42 of 42

Density [g·cm-3]

1.4325

Reference Temperature [°C]

25

Measurement Temperature 25 [°C] Perkin; Journal fuer Praktische Chemie (Leipzig); vol. <2>31; (1885); p. 500, View in Reaxys Adsorption (MCS) (29) 1 of 29

Description (Adsorption (MCS))

Adsorption isotherm

Partner (Adsorption (MCS))

KCl

Mitchenko, S. A.; Dadali, Yu. V.; Russian Journal of Organic Chemistry; vol. 35; nb. 3; (1999); p. 349 - 353; Zhurnal Organicheskoi Khimii; vol. 35; nb. 3; (1999); p. 375 - 379, View in Reaxys 2 of 29

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

-173.15 - 26.85

Partner (Adsorption (MCS))

GaAs(110)

Khan; Camillone III; Osgood Jr.; Journal of Chemical Physics; vol. 110; nb. 21; (1999); p. 10526 - 10538, View in Reaxys 3 of 29

Description (Adsorption (MCS))

Desorption

Partner (Adsorption (MCS))

GaAs

Khan, Khalid A.; Camillone III, Nicholas; Osgood Jr., Richard M.; Journal of Physical Chemistry B; vol. 103; nb. 26; (1999); p. 5530 - 5542, View in Reaxys 4 of 29

Description (Adsorption (MCS))

Adsorption

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Solvent (Adsorption (MCS))

diethyl ether; benzene

Temperature (Adsorption (MCS)) [°C]

3.85

Partner (Adsorption (MCS))

Mg

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 12; (1998); p. 1876 - 1877, View in Reaxys 5 of 29

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

21.9 - 99.9

Partner (Adsorption (MCS))

graphitized thermal carbon black

Kalashnikova; Lopatkin; Russian Chemical Bulletin; vol. 46; nb. 12; (1997); p. 2060 - 2063, View in Reaxys 6 of 29

Description (Adsorption (MCS))

Enthalpy of adsorption

Solvent (Adsorption (MCS))

benzene

Partner (Adsorption (MCS))

magnesium

Maslennikov; Kirillov; Berezina; Spirina; Kondin; Russian Journal of General Chemistry; vol. 67; nb. 5; (1997); p. 667 671, View in Reaxys 7 of 29

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

-183.15 - 566.85

Pressure (Adsorption (MCS)) [Torr]

0

Partner (Adsorption (MCS))

GaAs(110)

Khan, Khalid A.; Moryl, Joseph E.; Slater, David A.; Lasky, Peter J.; Osgood Jr., Richard M.; Journal of Physical Chemistry B; vol. 101; nb. 44; (1997); p. 9077 - 9086, View in Reaxys 8 of 29

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

-148.1 - 26.9

Partner (Adsorption (MCS))

Cu(100)

Lin, Jong-Liang; Teplyakov, Andrew V.; Bent, Brian E.; Journal of Physical Chemistry; vol. 100; nb. 25; (1996); p. 10721 10731, View in Reaxys 9 of 29

Description (Adsorption (MCS))

Desorption

Solvent (Adsorption (MCS))

neat (no solvent)

Temperature (Adsorption (MCS)) [°C]

-173.1 - 126.9

Partner (Adsorption (MCS))

Cu(111)

Lin, Jong-Liang; Bent, Brian E.; Journal of Physical Chemistry; vol. 96; nb. 21; (1992); p. 8529 - 8538, View in Reaxys 10 of 29

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

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Solvent (Adsorption (MCS))

neat (no solvent)

Temperature (Adsorption (MCS)) [°C]

-158.1 - -153.1

Partner (Adsorption (MCS))

Cu(111)

Lin, Jong-Liang; Bent, Brian E.; Journal of Physical Chemistry; vol. 96; nb. 21; (1992); p. 8529 - 8538, View in Reaxys 11 of 29

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

poly(styrene-co-divinylbenzene) <Poly(Sty-co-DVB)>

Errede, L. A.; Journal of Physical Chemistry; vol. 95; nb. 4; (1991); p. 1836 - 1843, View in Reaxys 12 of 29

Description (Adsorption (MCS))

Enthalpy of adsorption

Zaprometov et al.; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 708; ; p. 1230, View in Reaxys; Kiselev et al.; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 705,706; ; p. 1272, View in Reaxys 13 of 29

Description (Adsorption (MCS))

Adsorption

Oehme; Angewandte Chemie; vol. 72; (1960); p. 489, View in Reaxys 14 of 29

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

Ni

Orient, O.; Acta Physica Academiae Scientiarum Hungaricae; vol. 7; (1957); p. 199 - 206; C. A.; (1957); p. 16078, View in Reaxys; Orient, O.; Acta Physica Academiae Scientiarum Hungaricae; vol. 9; (1959); p. 343 - 345; N. S. A.; vol. 13; (1959); p. 13464, View in Reaxys; Orient, O.; Magy. Tud. Akad. Kozp. Fiz. Kut. Int. Kozlemen.; vol. 5; (1957); p. 577 - 581; N. S. A.; vol. 12; (1958); p. 16577, View in Reaxys; vol. Ni: MVol.AII1; 102, page 371 - 390 ; (from Gmelin), View in Reaxys 15 of 29

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

an Zeolithe.

Barrer; Journal of the Society of Chemical Industry, London; vol. 64; (1945); p. 131, View in Reaxys 16 of 29

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

20

Comment (Adsorption (MCS))

an Chabasit.

Partner (Adsorption (MCS))

methanol

Barrer; Journal of the Society of Chemical Industry, London; vol. 64; (1945); p. 134, View in Reaxys 17 of 29

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

97

Comment (Adsorption (MCS))

an Chabasit.

Partner (Adsorption (MCS))

1,1-dichloroethane

Barrer; Journal of the Society of Chemical Industry, London; vol. 64; (1945); p. 134, View in Reaxys 18 of 29

Description (Adsorption (MCS))

Adsorption

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Temperature (Adsorption (MCS)) [°C]

112

Comment (Adsorption (MCS))

an Chabasit.

Partner (Adsorption (MCS))

benzene

Barrer; Journal of the Society of Chemical Industry, London; vol. 64; (1945); p. 134, View in Reaxys 19 of 29

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

100

Comment (Adsorption (MCS))

an Kohle und Silicagel.

Magnus; Teller; Z.VDI Beih.Verfahrenstech.; (1939); p. 6; Chem. Zentralbl.; vol. 110; nb. II; (1939); p. 45, View in Reaxys 20 of 29

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

100

Comment (Adsorption (MCS))

an Kohle und Silicagel.

Partner (Adsorption (MCS))

ethene

Magnus; Teller; Z.VDI Beih.Verfahrenstech.; (1939); p. 6; Chem. Zentralbl.; vol. 110; nb. II; (1939); p. 45, View in Reaxys 21 of 29

Partner (Adsorption (MCS))

silica gel;

Magnus, A.; Teller, F.; Z. Vereins Dtsch. Ing. Verfahrenstechn.; (1939); p. 1 - 9 ; (from Gmelin), View in Reaxys 22 of 29

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

Waermetoenung von Aethylbromid-Dampf.

Partner (Adsorption (MCS))

charcoal

Alexejewski; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 708, View in Reaxys 23 of 29

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

silica gel;

Okatov, A.; Zhurnal prikladnoi Khim. (russ.); vol. 2; (1929); p. 21 - 84; C. II; (1929); p. 707, View in Reaxys; vol. Si: MVol.B; 187, page 529 - 531 ; (from Gmelin), View in Reaxys 24 of 29

Description (Adsorption (MCS))

Adsorption

Temperature (Adsorption (MCS)) [°C]

30

Comment (Adsorption (MCS))

an Kieselsaeure-Gele.

Holmes; Bulletin de la Societe Chimique de France; vol. <4>43; (1928); p. 285, View in Reaxys 25 of 29

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

iron hydroxide

Perry; Chem. Zentralbl.; vol. 98; nb. II; (1927); p. 1549, View in Reaxys

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26 of 29

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

Geschwindigkeit.

Partner (Adsorption (MCS))

coconut coal

Tryhorn; Wyatt; Transactions of the Faraday Society; vol. 22; p. 137; Chem. Zentralbl.; vol. 97; nb. II; (1926); p. 1518, View in Reaxys 27 of 29

Description (Adsorption (MCS))

Adsorption

Partner (Adsorption (MCS))

mercury

Iredale; Chem. Zentralbl.; vol. 96; nb. I; (1925); p. 1960, View in Reaxys 28 of 29

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

Dampf.

Partner (Adsorption (MCS))

charcoal

Alexejewski; Zhurnal Russkago Fiziko-Khimicheskago Obshchestva; vol. 55; (1924); p. 416; Chem. Zentralbl.; vol. 96; nb. II; (1925); p. 642, View in Reaxys 29 of 29

Description (Adsorption (MCS))

Adsorption

Comment (Adsorption (MCS))

Waermetoenung von Aethylbromid-Dampf.

Partner (Adsorption (MCS))

active coal

Lamb; Coolidge; Journal of the American Chemical Society; vol. 42; (1920); p. 1154, View in Reaxys Association (MCS) (18) 1 of 18

Description (Association (MCS))

Association with compound

Partner (Association (MCS))

calf thymus DNA

Zhu, Li-Na; Gao, Huan-Rui; Wang, Hai-Xian; Xu, Ming-Yuan; Li, Xiao-Zeng; European Journal of Inorganic Chemistry; nb. 14; (2014); p. 2396 - 2405, View in Reaxys; Arun; Packianathan; Malarvizhi; Antony; Raman; Journal of Photochemistry and Photobiology B: Biology; vol. 149; (2015); p. 93 - 102, View in Reaxys 2 of 18

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

aq. buffer

Partner (Association (MCS))

fish sperm DNA

Ma, Chi; Liang, Shi-Kai; Zhao, Fu-Chen; Meng, Yang; Li, Ying-Ying; Zhu, Ming-Chang; Gao, En-Jun; Journal of Coordination Chemistry; vol. 67; nb. 21; (2014); p. 3551 - 3564, View in Reaxys 3 of 18

Description (Association (MCS))

Enthalpy of association

Solvent (Association (MCS))

tetrachloromethane

Temperature (Association (MCS)) [°C]

24.84

Partner (Association (MCS))

4-Fluorophenol

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Laurence, Christian; Graton, Jerome; Berthelot, Michel; Besseau, Francois; Le Questel, Jean-Yves; Lucon, Maryvonne; Ouvrard, Carole; Planchat, Aurelien; Renault, Eric; Journal of Organic Chemistry; vol. 75; nb. 12; (2010); p. 4105 - 4123, View in Reaxys 4 of 18

Description (Association (MCS))

Association with compound

Solvent (Association (MCS))

aq. buffer

Partner (Association (MCS))

calf thymus DNA

Li, Yong; Yang, Zheng-Yin; Journal of Fluorescence; vol. 20; nb. 1; (2010); p. 329 - 342, View in Reaxys 5 of 18

Description (Association (MCS))

IR spectrum of the complex

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

4-Fluorophenol

Ouvrard, Carole; Berthelot, Michel; Laurence, Christian; Journal of the Chemical Society. Perkin Transactions 2; nb. 7; (1999); p. 1357 - 1362, View in Reaxys 6 of 18

Description (Association (MCS))

Stability constant of the complex with ...

Solvent (Association (MCS))

CCl4

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

4-Fluorophenol

Ouvrard, Carole; Berthelot, Michel; Laurence, Christian; Journal of the Chemical Society. Perkin Transactions 2; nb. 7; (1999); p. 1357 - 1362, View in Reaxys 7 of 18

Description (Association (MCS))

Enthalpy of association

Partner (Association (MCS))

Br-

Li, Chun; Ross, Philip; Szulejko, Jan E.; McMahon, Terrance B.; Journal of the American Chemical Society; vol. 118; nb.

39; (1996); p. 9360 - 9367, View in Reaxys 8 of 18

Description (Association (MCS))

Enthalpy of association

Partner (Association (MCS))

Cl-

Li, Chun; Ross, Philip; Szulejko, Jan E.; McMahon, Terrance B.; Journal of the American Chemical Society; vol. 118; nb.

39; (1996); p. 9360 - 9367, View in Reaxys 9 of 18

Description (Association (MCS))

Further physical properties of the complex

Solvent (Association (MCS))

H2O

Partner (Association (MCS))

β-cyclodextrin; 1-Chloronaphthalene

Wei, Yan-Sheng; Jin, Wei-Jun; Zhu, Ruo-Hua; Xing, Guo-Wen; Liu, Chang-Song; Zhang, Shu-Se; Zhou, Bai-Ling; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 52; nb. 6; (1996); p. 683 - 690, View in Reaxys 10 of 18

Description (Association (MCS))

Further physical properties of the complex

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Solvent (Association (MCS))

H2O

Partner (Association (MCS))

β-cyclodextrin; 2-bromonaphthalene

Wei, Yan-Sheng; Jin, Wei-Jun; Zhu, Ruo-Hua; Xing, Guo-Wen; Liu, Chang-Song; Zhang, Shu-Se; Zhou, Bai-Ling; Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy; vol. 52; nb. 6; (1996); p. 683 - 690, View in Reaxys 11 of 18

Description (Association (MCS))

UV/VIS spectrum of the complex

Solvent (Association (MCS))

cyclohexane

Temperature (Association (MCS)) [°C]

22

Partner (Association (MCS))

Br atom

Alfassi, Zeev B.; Huie, Robert E.; Mittal, Jai P.; Neta, P.; Shoute, Lian C. T.; Journal of Physical Chemistry; vol. 97; nb. 36; (1993); p. 9120 - 9123, View in Reaxys 12 of 18

Description (Association (MCS))

UV/VIS spectrum of the complex

Temperature (Association (MCS)) [°C]

22

Partner (Association (MCS))

Br atom

Alfassi, Zeev B.; Huie, Robert E.; Mittal, Jai P.; Neta, P.; Shoute, Lian C. T.; Journal of Physical Chemistry; vol. 97; nb. 36; (1993); p. 9120 - 9123, View in Reaxys 13 of 18

Description (Association (MCS))

Association with compound

Temperature (Association (MCS)) [°C]

23

Partner (Association (MCS))

poly(styrene-co-divinylbenzene)

Errede, L. A.; Journal of Physical Chemistry; vol. 96; nb. 8; (1992); p. 3537 - 3542, View in Reaxys 14 of 18

Description (Association (MCS))

Further physical properties of the complex

Partner (Association (MCS))

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 15 of 18

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 16 of 18

Description (Association (MCS))

Association with compound

Voigt; Journal of Physical Chemistry; vol. 72; (1968); p. 3300, View in Reaxys 17 of 18

Description (Association (MCS))

Spectrum of the complex

Lunazzi; Taddei; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1479,1480, View in Reaxys; Pajak; Acta Physica Polonica; vol. 21; (1962); p. 131,138, View in Reaxys 18 of 18

Description (Association (MCS))

Enthalpy of association

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Ott; Snow; Journal of Physical Chemistry; vol. 67; (1963); p. 515, View in Reaxys Azeotropes (MCS) (21) 1 of 21

Kudrjawzewa et al.; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 688; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1285, View in Reaxys

2 of 21

Temperature (Azeotropes (MCS)) [°C]

38.2

Azeotropes

formic acid

Lecat; Ann.Soc.scient.Bruxelles; vol. 49; p. 33; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 396, View in Reaxys 3 of 21

Temperature (Azeotropes (MCS)) [°C]

37.7

Azeotropes

isopropyl nitrite

Lecat; Ann.Soc.scient.Bruxelles; vol. 48; p. I,55; Chem. Zentralbl.; vol. 99; nb. II; (1928); p. 854, View in Reaxys 4 of 21

Temperature (Azeotropes (MCS)) [°C]

37.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

alcohol

Lecat; La tension de vapeur des melanges de liquides - L'azeotropisme <Gent-Bruessel 1918>,S.83, View in Reaxys 5 of 21

Temperature (Azeotropes (MCS)) [°C]

32.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isoprene

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.282, View in Reaxys 6 of 21

Temperature (Azeotropes (MCS)) [°C]

32.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

n-pentane

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.282, View in Reaxys 7 of 21

Temperature (Azeotropes (MCS)) [°C]

37.6

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

ethanol

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.73, View in Reaxys 8 of 21

Temperature (Azeotropes (MCS)) [°C]

35

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methanol

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.71, View in Reaxys 9 of 21

Temperature (Azeotropes (MCS)) [°C]

23.7

Pressure (Azeotropes (MCS)) [Torr]

760

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Azeotropes

isopentane

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.282, View in Reaxys 10 of 21

Temperature (Azeotropes (MCS)) [°C]

37.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

cyclopentane

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.282, View in Reaxys 11 of 21

Azeotropes

methanol; CS2

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.261,262,263, View in Reaxys; Lecat,M.; L'Azeotropisme, 1.Aufl.Teil 2<Bruessel 1918> S.185,187,195, View in Reaxys 12 of 21

Temperature (Azeotropes (MCS)) [°C]

38.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

dichloromethane

Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.279, View in Reaxys; Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys 13 of 21

Temperature (Azeotropes (MCS)) [°C]

38.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

formic acid

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.12, View in Reaxys 14 of 21

Temperature (Azeotropes (MCS)) [°C]

37

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

dimethyl sulfide

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.302, View in Reaxys 15 of 21

Temperature (Azeotropes (MCS)) [°C]

37.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopropyl nitrite

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.228, View in Reaxys 16 of 21

Temperature (Azeotropes (MCS)) [°C]

35

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

trimethylethylene

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.282, View in Reaxys 17 of 21

Temperature (Azeotropes (MCS)) [°C]

37.8

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Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

carbon disulfide

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.302, View in Reaxys 18 of 21

Temperature (Azeotropes (MCS)) [°C]

36.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

β.β-dimethyl-allene

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.282, View in Reaxys 19 of 21

Temperature (Azeotropes (MCS)) [°C]

29.9

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

formic acid methyl ester

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.50, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949> S.228, View in Reaxys 20 of 21

Azeotropes

methanol; 2-methyl-butene-(2)

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.261,262,263, View in Reaxys; Lecat,M.; L'Azeotropisme, 1.Aufl.Teil 2<Bruessel 1918> S.185,187,195, View in Reaxys 21 of 21

Azeotropes

2-methyl-butane; formic acid methyl ester

Horsley,L.H.; in Azeotropic Data (=Advances in Chemistry Series Nr.6) <Washington 1952>S.261,262,263, View in Reaxys; Lecat,M.; L'Azeotropisme, 1.Aufl.Teil 2<Bruessel 1918> S.185,187,195, View in Reaxys Boundary Surface Phenomena (MCS) (3) 1 of 3

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Pilpel; Transactions of the Faraday Society; vol. 56; (1960); p. 893,898, View in Reaxys 2 of 3

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

gegen Wasser bei 25grad.

Donahue; Bartell; Journal of Physical Chemistry; vol. 56; (1952); p. 480,483, View in Reaxys 3 of 3

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

zwischen Aethylbromid und Wasser.

Harkins; Clark; Roberts; Journal of the American Chemical Society; vol. 42; (1920); p. 703, View in Reaxys Compressibility (11) Description (Com- Comment (Compressibility) pressibility)

References

Adiabatic compres- bei 10grad. sibility

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

Adiabatic compres- bei 20grad. sibility

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

Adiabatic compres- bei 30grad. sibility

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

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Isothermal compressibility

bei 50grad unter Bridgman; Journal of Chemical Physics; vol. 9; (1941); p. 797; Pr.am.Acad.Arts Sci.; vol. 77; p.

Drucken zwischen 142; Chem.Abstr.; (1949); p. 4067, View in Reaxys 5000 und 50000 kg/ cmE2.

Adiabatic compres- bei 28grad. sibility

Parthasarathy; Proceedings - Indian Academy of Sciences, Section A; vol. 3; p. 520; Chem. Zentralbl.; vol. 107; nb. II; (1936); p. 2083, View in Reaxys

Adiabatic compres- zwischen 1 und 2 sibility Atm. Druck bei 0-32grad:.

Tyrer; Journal of the Chemical Society; vol. 105; (1914); p. 2538, View in Reaxys

Isothermal compressibility

zwischen 1-18 Atm. bei 13.7grad: 113.4*10E-6 AtmE-1.

Tyrer; Journal of the Chemical Society; vol. 105; (1914); p. 2538, View in Reaxys; Suchodski; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 74; (1910); p. 267,271, View in Reaxys

Isothermal compressibility

zwischen 1-18 Atm. bei 35.0grad: 138.4*10E-6 AtmE-1.

Tyrer; Journal of the Chemical Society; vol. 105; (1914); p. 2538, View in Reaxys; Suchodski; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 74; (1910); p. 267,271, View in Reaxys

Adiabatic compres- zwischen 1 und 2 sibility Atm. Druck bei 0grad und 23grad.

Gay; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 156; (1913); p. 1979; Annales de Physique (Paris, France); vol. <9>6; (1916); p. 127, View in Reaxys

Isothermal compressibility

bei 20grad zwischen 100 und 500 megabar: 90.7*10E-6 cm2/ megadyn.

Richards; Stull; Mathews; Speyers; Journal of the American Chemical Society; vol. 34; (1912); p. 989, View in Reaxys

Isothermal compressibility

und Ausdehnung zwischen 20grad und 80grad bei Drucken von 1-12000 kg/cmE2.

Bridgman; Pr.am.Acad.Arts Sci.; 49<94>,70,87, View in Reaxys

Conformation (3) Object of Investiga- References tion Conformer equilibrium

Ferner, S.; Salzer, R.; Borsdorf, R.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 264; nb. 1; (1983); p. 178 180, View in Reaxys

Energy difference between the conformers

Heublein,G. et al.; Tetrahedron; vol. 26; (1970); p. 81 - 90, View in Reaxys

Conformation

Bentley,F.F. et al.; Spectrochimica Acta; vol. 20; (1964); p. 105 - 126, View in Reaxys; Tabacik; Tetrahedron Letters; (1968); p. 555, View in Reaxys

Critical Density (1) Critical Density References [g·cm-3] 0.507

Herz; Neukirch; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 104; (1923); p.

444, View in Reaxys

Critical Pressure (1) Critical Pressure References [Torr] 46740

Herz; Neukirch; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 104; (1923); p.

444, View in Reaxys

Critical Temperature (3) Critical TemperaReferences ture [°C] 230.85

Filippov, L. P.; Laushkina, L. A.; Russian Journal of Physical Chemistry; vol. 58; nb. 5; (1984); p. 654 - 656; Zhurnal Fizicheskoi Khimii; vol. 58; (1984); p. 1072 - 1077, View in Reaxys

230.8

Herz; Neukirch; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 104; (1923); p.

444, View in Reaxys Pawlewski; Chemische Berichte; vol. 16; (1883); p. 2634, View in Reaxys

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Critical Volume (2) Critical Volume [l/ References mol] 0.21

Filippov, L. P.; Laushkina, L. A.; Russian Journal of Physical Chemistry; vol. 58; nb. 5; (1984); p. 654 - 656; Zhurnal Fizicheskoi Khimii; vol. 58; (1984); p. 1072 - 1077, View in Reaxys Bhagvanth Rao et al.; Journal of the Indian Institute of Science; vol. 53; (1971); p. 99,103, View in Reaxys

Cross-Sections (2) Description (Cross- Comment (CrossSections) Sections)

References

Collision cross-section

Herrero, V. J.; Rabanos V. Saez; Urena, A. Gonzales; Journal of Physical Chemistry; vol. 88; nb. 11; (1984); p. 2339 - 2343, View in Reaxys; Khan; Camillone III; Osgood Jr.; Journal of Chemical Physics; vol. 110; nb. 21; (1999); p. 10526 - 10538, View in Reaxys

Collision cross-sec- mit Kalium-Atomtion en.

Rothe; Bernstein; Journal of Chemical Physics; vol. 31; (1959); p. 1619,1622, View in Reaxys

Crystal Phase (3) Description (Crystal Phase)

Comment (Crystal Phase)

References

Crystal structure determination

.; Method of determination: X-ray Diffraction

Mager, T.; Schultz, E.; Bertagnolli, H.; Frahm, R.; Berichte der Bunsen-Gesellschaft; vol. 94; nb. 6; (1990); p. 703 - 709, View in Reaxys

Crystal structure determination

.; Temperature: 25 Bertagnolli, H.; Schulz, G.; Berichte der Bunsen-Gesellschaft; vol. 90; (1986); p. 816 - 823, C. Method of deter- View in Reaxys mination: X-ray Diffraction

Crystal structure determination

v.Stackelberg; Mueller; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 58; (1954); p. 25,26, View in Reaxys

Crystal Property Description (2) Colour & Other Location Properties

References

white

Paragraph 0194

yellow

supporting informa- McKeever, Caitriona; Kaiser, Marcel; Rozas, Isabel; Journal of Medicinal Chemistry; vol. 56; tion nb. 3; (2013); p. 700 - 711, View in Reaxys

Dielectric Constant (20) Dielectric Constant Frequency (Dielectric Constant) [Hz] 9.59

2E+06

Patent; BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM; MARTIN, Stephen, F.; SAHN, James, J.; LINKENS, Kathryn, Taylor; (119 pag.); WO2017/190109; (2017); (A1) English, View in Reaxys

Temperature (Dielectric Constant) [°C]

Comment (Dielectric Constant)

20

References

Laurence, Christian; Nicolet, Pierre; Dalati, M. Tawfik; Abboud, Jose-Luis M.; Notario, Rafael; Journal of Physical Chemistry; vol. 98; nb. 23; (1994); p. 5807 - 5816, View in Reaxys Turner; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 35; (1900); p. 428, View in Reaxys; Drude; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 23; (1897); p. 311; Chemische Berichte; vol. 30; (1897); p. 961, View in Reaxys; Zaugg; Journal of the American Chemical Society; vol. 82; (1960); p. 2903,2905, View in Reaxys; Piekara; Acta Physica Polonica; vol. 18; (1959); p.

361,362-376; Chem.Abstr.; nb. 14841; (1960), View in Reaxys; Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p. 207, View in Reaxys; Bellomo et al.; Annali di Chimica (Rome, Italy); vol. 55; (1965); p. 832,838, View in Reaxys; Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys; Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol.

71; (1974); p. 673,678, View in Reaxys; Strat et al.;

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Journal of Applied Spectroscopy; vol. 18; (1973); p.

198; ; p. 263, View in Reaxys 9.24

3E+09

25

Branin; Smyth; Journal of Chemical Physics; vol. 20; (1952); p. 1121,1124, View in Reaxys

10.2

3E+09

1

Branin; Smyth; Journal of Chemical Physics; vol. 20; (1952); p. 1121,1124, View in Reaxys

8.87

9.31677E+09

25

Laquer; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4100, View in Reaxys

9.5

9.31677E+09

1

Laquer; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4100, View in Reaxys

8.32

1E+10

25

Crouch; Journal of Chemical Physics; vol. 16; (1948); p. 364, View in Reaxys

7.09

2.3622E+10

1

Heston; Hennelly; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4096, View in Reaxys

9.5

1E+06

20

Tschamler; Monatshefte fuer Chemie; vol. 78; (1948); p. 297,304; Monatshefte fuer Chemie; vol. 79; (1948); p. 162,169, View in Reaxys

7.29

2.3622E+10

25

Heston; Hennelly; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4096, View in Reaxys; Hennelly; Heston; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p.

4105, View in Reaxys

11.69 - 8.59

2E+06

-30 - 35

Le Fevre; Transactions of the Faraday Society; vol.

34; (1938); p. 1130, View in Reaxys

17.05 - 8.44

-100 - 40

Morgan; Lowry; Journal of Physical Chemistry; vol.

34; (1930); p. 2411, View in Reaxys

1.01 - 1.01

29.8 - 116.8

16.22 - 8.67

500000

Static Dielectric constant:Dampf und 760 mm.

-92.3 - 35.5

Mahanti; Gupta; Indian J.Phys.; vol. 3; p. 192; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 1309, View in Reaxys Smyth; Morgan; Journal of the American Chemical Society; vol. 50; (1928); p. 1554, View in Reaxys

1.02

15

Static Dielectric constant:Dampf und 760 mm.

1.01

17

Pohrt; Annalen der Physik (Weinheim, Germany); vol. <4>42; (1913); p. 581, View in Reaxys

1.01

99.6

Pohrt; Annalen der Physik (Weinheim, Germany); vol. <4>42; (1913); p. 581, View in Reaxys

9.4

21

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 575, View in Reaxys

10.5

1.4

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 70; (1910); p. 575, View in Reaxys

9.28793E+09 Dissociation Energy (4) Dissociation Ener- Bond Type gy [Jmol-1]

Cordonnier; Guinchant; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 185; (1927); p. 1449, View in Reaxys

Srivastava; Swarup; Journal of Scientific and Industrial Research; 15<B<1956>231, View in Reaxys References

394396

C(1)-H

Holmes, John L.; Lossing, F. P.; Journal of the American Chemical Society; vol. 110; nb. 22; (1988); p. 7343 - 7345, View in Reaxys

415330

C(2)-H

Holmes, John L.; Lossing, F. P.; Journal of the American Chemical Society; vol. 110; nb. 22; (1988); p. 7343 - 7345, View in Reaxys Williams; Hamill; Journal of Chemical Physics; vol. 49; (1968); p. 4467,4476, View in Reaxys; Coomber; Whittle; Transactions of the Faraday Society; vol. 63; (1967); p. 608,619,

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View in Reaxys; Coomber; Whittle; Transactions of the Faraday Society; vol. 63; (1967); p.

2656,2666, View in Reaxys; Meschkowa et al.; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 925; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1708, View in Reaxys; Yeranos; Journal of Chemical Physics; vol. 50; (1969); p. 3670,3673, View in Reaxys; Ashcroft et al.; Transactions of the Faraday Society; vol. 61; (1965); p. 225,229, View in Reaxys; Maslow; Russian Journal of Physical Chemistry; vol. 35; (1961); p. 762; Zhurnal Fizicheskoi Khimii; vol. 35; (1961); p. 1551, View in Reaxys; Mantashyan; Nalbandyan; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1731; ; p. 3030, View in Reaxys Br-C2H5

Dynamic Viscosity (12) Dynamic Viscosity Temperature (Dy[P] namic Viscosity) [°C]

Szwarc; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 207; (1951); p. 5,13, View in Reaxys; Mortimer et al.; Transactions of the Faraday Society; vol. 48; (1952); p. 220,225, View in Reaxys; Irsa; Journal of Chemical Physics; vol. 26; (1957); p. 18,19, View in Reaxys References

0.004

19.9

Abramzon, A. A.; Pankratov, V. A.; Cherpalova, T. M.; J. Appl. Chem. USSR (Engl. Transl.); vol. 61; nb. 6; (1988); p. 1266 - 1271,1159 - 1163, View in Reaxys

0.001765 0.003964

20 - 120

Rutherford, W. M.; Journal of Chemical & Engineering Data; vol. 33; nb. 3; (1988); p. 234 - 237, View in Reaxys

0.00482

1

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2071,2072, View in Reaxys

0.00397

20

Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys

0.00383

25

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2071,2072, View in Reaxys

0.00379

25

Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys

0.003678 0.004866

0 - 30

Irany; Journal of the American Chemical Society; vol. 61; (1939); p. 1441, View in Reaxys; Heydweiller; Annalen der Physik (Weinheim, Germany); <N.F.>59<1896>199, View in Reaxys

0.00368

30

Bridgman; Proceedings of the National Academy of Sciences of the United States of America; vol. 11; p. 604; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 1923, View in Reaxys; Bridgman; Pr.am.Acad.Arts Sci.; vol. 61; (1925); p. 70,78; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 1919, View in Reaxys

0.00418

15

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

0.00348

30

Timmermans; Martin; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 23; (1926); p. 756, View in Reaxys

-120 - -80

Kanolt; Scient.Pap.Bur.Stand.; 19/20<926>,630, View in Reaxys Thorpe; Rodger; Transact. Royal Soc.A; vol. 185; p. 472, View in Reaxys

Electrical Data (10) 1 of 10

Description (Electrical Da- Electrical conductivity ta) Kopylov; Yanchenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 243; ; p. 421, View in Reaxys

2 of 10

Description (Electrical Da- Piezoelectricity ta) Heel; Zeil; Zeitschrift fuer Elektrochemie; vol. 64; (1960); p. 962,963-971; Chem.Abstr.; vol. 55; nb. 115; (1961), View in Reaxys

3 of 10

Description (Electrical Da- Electrical conductivity ta) Comment (Electrical Data) Erhoehung bei der Einwirkung von Ultraschall.

Berkowitz; Canadian Journal of Chemistry; vol. 37; (1959); p. 13,16, View in Reaxys

4 of 10

Description (Electrical Da- Photoelectricity (Becquerel effect) ta) Comment (Electrical Data) bei einer Loesung in Aethanol.

Levin et al.; Journal of Chemical Physics; vol. 21; (1953); p. 1654,1655, View in Reaxys

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5 of 10

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) β:10 cm;bei 1grad und 25grad.

Branin; Smyth; Journal of Chemical Physics; vol. 20; (1952); p. 1121,1124, View in Reaxys

6 of 10

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von Gemischen mit Hexadecan bei 20grad,30grad,und 40grad ; auch Dielektrizitaetskonstante.

Heston et al; Journal of the American Chemical Society; vol. 72; (1950); p. 3443,3446, View in Reaxys

7 of 10

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) von binaeren Gemischen mit Heptan, Hexadecan,Cyclohexan und Benzol bei 0grad,20grad,und 40grad ; auch Dielektrizitaetskonstante.

Franklin et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 3447,3452, View in Reaxys

8 of 10

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) bei 1grad und bei 25grad (β=1-3 cm).

Heston; Hennelly; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4096, View in Reaxys; Laquer; Smyth; Journal of the American Chemical Society; vol. 70; (1948); p. 4100, View in Reaxys; Crouch; Journal of Chemical Physics; vol. 16; (1948); p. 364, View in Reaxys

9 of 10

Description (Electrical Da- Dielectric strength ta) Comment (Electrical Data) des Dampfes.

Hochberg; Sandberg; Zhurnal Tekhnicheskoi Fiziki; vol. 12; (1942); p. 65; Chem.Abstr.; (1943); p. 1326, View in Reaxys; Thornton; Phil.Mag.; vol. <7>28; (1939); p. 669, View in Reaxys; Dobretzow; Doklady Akademii Nauk SSSR; vol. 59; (1948); p. 1547; Chem.Abstr.; (1949); p. 454, View in Reaxys; Sandberg; Zhurnal Tekhnicheskoi Fiziki; vol. 17; (1947); p. 299; Chem.Abstr.; (1948); p. 814, View in Reaxys

10 of 10

Description (Electrical Da- Dielectric loss ta) Comment (Electrical Data) in Benzolloesung (β=7 m).

Henrion; Bulletin de la Societe Royale des Sciences de Liege; vol. 8; (1939); p. 333; Bulletin de la Societe Royale des Sciences de Liege; vol. 10; (1941); p. 416; Chem. Zentralbl.; 1940 I 851,1942 I 26, View in Reaxys

Electrical Moment (18) 1 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.72

Borovikov; Makovetskii; Pivovarova; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 100; nb. 1; (1996); p. 33 - 38, View in Reaxys 2 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.04

Hayashi, Michiro; Fujitake, Masaharu; Inagusa, Tohihiro; Miyazaki, Sonoko; Journal of Molecular Structure; vol. 216; (1990); p. 9 - 26, View in Reaxys 3 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.03

Jung, Kyung-Hoon; Kang, Sung Hoon; Ro, Chul Un; Tschuikow-Roux, E.; Journal of Physical Chemistry; vol. 91; nb. 9; (1987); p. 2354 - 2358, View in Reaxys 4 of 18

Description (Electrical Moment)

Dipole moment

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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 5 of 18

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ (unverduennt)

Vuks; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 1239; Zhurnal Fizicheskoi Khimii; vol. 43; (1969); p. 2208, View in Reaxys 6 of 18

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

unverd.

Vaks; Sov. Phys. Dokl. (Engl. Transl.); vol. 12; (1967); p. 801,325, View in Reaxys 7 of 18

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Dipolmoment (β; Dampf; bei 35grad): 2.069 D

Weiss; Journal of Physical Chemistry; vol. 70; (1966); p. 3146, View in Reaxys 8 of 18

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

scheinbares Dipolmoment: μ=1.93 D (CCl4)

Le Fevre; Williams; Journal of the Chemical Society; (1965); p. 4185, View in Reaxys 9 of 18

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ=1.90 D

Pilpel; Transactions of the Faraday Society; vol. 56; (1960); p. 893,898, View in Reaxys 10 of 18

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

in Benzol

Krishna; Srivastava; Journal of Chemical Physics; vol. 32; (1960); p. 663, View in Reaxys 11 of 18

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ=1.8 D

Zaugg; Journal of the American Chemical Society; vol. 82; (1960); p. 2903,2905, View in Reaxys 12 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.01

Method (Electrical Moment)

Dielectric constant (β)

Goss; Journal of the Chemical Society; (1940); p. 753, View in Reaxys; Groves; Sugden; Journal of the Chemical Society; (1937); p. 161,1996,2000, View in Reaxys 13 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.88 - 1.93

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Solvent (Electrical Moment)

benzene

Niini; Annales Academiae Scientiarum Fennicae, Series A; vol. 46; nb. 1; (1936); p. 101; Chem. Zentralbl.; vol. 108; nb. I; (1937); p. 570, View in Reaxys; Cowley; Partington; Journal of the Chemical Society; (1937); p. 130,131, View in Reaxys; Otto; Wenzke; Industrial and Engineering Chemistry, Analytical Edition; vol. 6; (1934); p. 187, View in Reaxys 14 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.99

Method (Electrical Moment)

Dielectric constant (β)

Mahanti; Phil.Mag.; vol. <7>20; (1935); p. 284, View in Reaxys 15 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.02

Method (Electrical Moment)

Dielectric constant (β)

Smyth; McAlpine; Journal of Chemical Physics; vol. 2; (1934); p. 501, View in Reaxys 16 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.78

Comment (Electrical Moment)

Dipolmoment::Dampf.

Mahanti; Gupta; Indian J.Phys.; vol. 3; p. 192; Chem. Zentralbl.; vol. 100; nb. I; (1929); p. 1309, View in Reaxys 17 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.08 - 2.09

Comment (Electrical Moment)

Dipolmoment::Dampf.

Hoejendahl; Phys.Z.; vol. 30; (1929); p. 392, View in Reaxys 18 of 18

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

1.86

Solvent (Electrical Moment)

hexane

Smyth; Morgan; Journal of the American Chemical Society; vol. 50; (1928); p. 1554, View in Reaxys Electrical Polarizability (4) Description (Elec- References trical Polarizability) Atom polarization

Rao; Thyagarajan; Indian Journal of Pure and Applied Physics; vol. 12; (1974); p. 242, View in Reaxys

Electron polarization

Hauchecorne et al.; Journal de Physique (Paris); vol. 32; (1971); p. 47,53-55, View in Reaxys

Optical anisotropy

Clement; Malaval; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1161,1165, View in Reaxys

Molar polarization

Boggs et al.; Journal of Physical Chemistry; vol. 63; (1959); p. 713, View in Reaxys; Le Fevre; Williams; Journal of the Chemical Society; (1965); p. 4185, View in Reaxys

Electrochemical Behaviour (3)

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Description (Electrochemical Behaviour)

References

Proton affinity

Polley; Munson; International Journal of Mass Spectrometry and Ion Physics; vol. 26; (1978); p. 49,52, 57-58, View in Reaxys

Electrochemical properties

Britz; Luft; Berichte der Bunsen-Gesellschaft; vol. 77; (1973); p. 836, View in Reaxys; Thiebault et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 285; (1977); p. 373, View in Reaxys

Polarography

Lambert; Kobayashi; Journal of the American Chemical Society; vol. 82; (1960); p. 5324,5326, View in Reaxys; Lambert; Journal of Organic Chemistry; vol. 31; (1966); p. 4184,4185, 4186, View in Reaxys; Butin et al.; Doklady Physical Chemistry; vol. 208-213; (1973); p. 633, View in Reaxys

Electrochemical Characteristics (5) 1 of 5

Description (Electrochemical Characteristics)

reduction potential

Goba; Turovska; Stradins; Turovskis; Liepinsh; Belyakov; Chemistry of Heterocyclic Compounds; vol. 43; nb. 2; (2007); p.

175 - 186, View in Reaxys 2 of 5

Description (Electrochemical Characteristics)

oxidation potential

Becker; Tetrahedron Letters; (1978); p. 1331,1332, View in Reaxys 3 of 5

Description (Electrochemical Characteristics)

polarographic half-wave potential

Thiebault et al.; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 285; (1977); p.

373, View in Reaxys; Fleischmann et al.; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 29; (1971); p. 325,326, View in Reaxys 4 of 5

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Wawzonek et al; J.electroch.Soc.; vol. 103; (1956); p. 456,457, View in Reaxys 5 of 5

Description (Electrochemical Characteristics)

polarographic half-wave potential

Comment (Electrochemical Characteristics)

bei der Elektrolyse in Dioxan bei Gegenwart von Tetraaethylammoniumbromid bei 25grad an der Quecksilbertropfelektrode.

von Stackelberg; Stracke; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 53; (1949); p. 122, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Modelli, Alberto; Scagnolari, Francesco; Distefano, Giuseppe; Jones, Derek; Guerra, Maurizio; Journal of Chemical Physics; vol. 96; nb. 3; (1992); p. 2061 - 2070, View in Reaxys

Energy Barriers (2) Energy Barriers Barrier Type [Jmol-1] 15407.4

C-C

References Lombardi, Erminio; Jansen, Laurens; Gazzetta Chimica Italiana; vol. 118; nb. 10; (1988); p.

715 - 724, View in Reaxys Nilsson,B. et al.; Journal of the American Chemical Society; vol. 96; (1974); p. 3190 - 3197, View in Reaxys; Monchick; Mason; Journal of Chemical Physics; vol. 35; (1961); p. 1676,1692, View in Reaxys; Scott; Scheraga; Journal of Chemical Physics; vol. 42; (1965); p. 2209,2214, View in Reaxys; Flanagan; Pierce; Journal of Chemical Physics; vol. 38; (1963); p. 2963,2964, View in Reaxys; Lowe; Parr; Journal of Chemical Physics; vol. 44; (1966); p. 3001,3003, View in Reaxys; Durig et al.; Journal of Chemical Physics; vol. 54; (1971); p. 460,462, 466, View in Reaxys; Lombardi et al.; Journal of Chemical Physics; vol. 61; (1974); p. 894,898, View in Reaxys; Durig et al.; Journal of Chemical Physics; vol. 60; (1974); p. 1754, View in Reaxys; Abraham; Parry; Journal of the Chemical Society [Section] B: Physical Organic; (1970); p. 539,541, View in Reaxys

Energy Data (MCS) (18) 1 of 18

Description (Energy Data (MCS))

Molar excess Gibbs free energy

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Temperature (Energy Data (MCS)) [°C]

25

Pressure (Energy Data (MCS)) [Torr]

760

Comment (Energy Data (MCS))

gas

Partner (Energy Data (MCS))

Hexadecane

Jamalizadeh; Hosseini; Russian Journal of Physical Chemistry A; vol. 80; nb. 9; (2006); p. 1423 - 1427, View in Reaxys 2 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

1-fluoropentane

Arial, Manuela; Embid, Jose Munoz; Otin, Santos; Velasco, Inmaculada; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol. 100; nb. 10; (1996); p. 1752 - 1758, View in Reaxys 3 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

1-iodo-butane

Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 6; (1994); p. 609 - 616, View in Reaxys 4 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

methyl iodide

Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 7; (1994); p. 703 - 708, View in Reaxys 5 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

2,2-Dimethylbutane

Lopez, M. C.; Royo, F. M.; Gracia, M.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 15; nb. 6; (1983); p.

517 - 522, View in Reaxys 6 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

cyclohexane

Lopez, M. C.; Royo, F. M.; Gracia, M.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 15; nb. 6; (1983); p.

517 - 522, View in Reaxys 7 of 18

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

bromine

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Makitra, R. G.; Pirig, Ya. N.; Tsvetkov, V. G.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 4; (1983); p. 727 - 732,633 638, View in Reaxys 8 of 18

Description (Energy Data (MCS))

Enthalpy of solution

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

n-heptane

Solomonov, B. N.; Gorbachuk, V. V.; Konovalov, A. I.; J. Gen. Chem. USSR (Engl. Transl.); vol. 52; nb. 12; (1982); p. 2688 2693,2370 - 2374, View in Reaxys 9 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Raetzsch et al.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 255; (1974); p. 115,124, View in Reaxys; Valero et al.; Journal of Chemical Thermodynamics; vol. 12; (1980); p. 627,629, View in Reaxys 10 of 18

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

bromine

Tsvetkov, V. G.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 2; (1980); p. 258 - 262,201 - 205, View in Reaxys 11 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

hexane

Valero, J.; Lopez, M. C.; Gracia, M.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 12; nb. 7; (1980); p.

627 - 634, View in Reaxys 12 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

dodecane

Valero, J.; Lopez, M. C.; Gracia, M.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 12; nb. 7; (1980); p.

627 - 634, View in Reaxys 13 of 18

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

Hexadecane

Valero, J.; Lopez, M. C.; Gracia, M.; Losa, C. Gutierrez; Journal of Chemical Thermodynamics; vol. 12; nb. 7; (1980); p.

627 - 634, View in Reaxys 14 of 18

Description (Energy Data (MCS))

Enthalpy of mixtures

Bezrukov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol.

20; (1971); p. 279,282; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 342, View in Reaxys; Karol; Sakharov; Theoretical and Experimental Chemistry; vol. 2; (1966); p. 487; ; p. 633, View in Reaxys 15 of 18

Description (Energy Data (MCS))

Thermodynamic properties of system with

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Abraham; Johnston; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1971); p. 1610,1611, View in Reaxys 16 of 18

Description (Energy Data (MCS))

Enthalpy of solution

Gukalova; Korol'; Russian Journal of Physical Chemistry; vol. 44; (1970); p. 652; ; p. 1171, View in Reaxys 17 of 18

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 18 of 18

Description (Energy Data (MCS))

Enthalpy of evaporation

Partner (Energy Data (MCS))

benzene

Tyrer; Journal of the Chemical Society; vol. 101; (1912); p. 85, View in Reaxys Enthalpy of Combustion (2) Enthalpy of ComComment (Enthalbustion [Jmol-1] py of Combustion)

References

-1.43113E+06

AethylbromidDampf.

Thomsen; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol.

52; (1905); p. 343; Thermochemische Untersuchungen; vol. 4; p. 104, View in Reaxys

-1.37955E+06

AethylbromidDampf.

Berthelot; Annales de Chimie (Cachan, France); vol. <5> 23; (1881); p. 209, View in Reaxys

Enthalpy of Formation (3) Enthalpy of Forma- Temperature (Ention [Jmol-1] thalpy of Formation) [°C]

-61965

Comment (Enthalpy of Formation)

References

Enthalpy of formation given

Borkar, Sampada; Sztaray, Balint; Journal of Physical Chemistry A; vol.

114; nb. 20; (2010); p. 6117 - 6123, View in Reaxys

25

Luo, Yu-Ran; Benson, Sidney W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5255 - 5257, View in Reaxys Bernstein; Journal of Physical Chemistry; vol. 69; (1965); p. 1550,1558, View in Reaxys; Cox; Tetrahedron; vol. 18; (1962); p. 1337,1342, View in Reaxys; Fowell et al.; Transactions of the Faraday Society; vol. 61; (1965); p. 1324,1326, View in Reaxys; Ashcroft et al.; Transactions of the Faraday Society; vol. 61; (1965); p. 225,229, View in Reaxys

Enthalpy of Fusion (3) Enthalpy of Fusion References [Jmol-1] 6196.46

Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys

5861.52

Sapgir; Bulletin des Societes Chimiques Belges; vol. 38; (1929); p. 394,406, View in Reaxys; Timmermans; Bulletin des Societes Chimiques Belges; vol. 43; (1934); p. 637, View in Reaxys

5924.32

Sapgir; Bulletin des Societes Chimiques Belges; vol. 38; (1929); p. 394,406, View in Reaxys

Enthalpy of Vaporization (5) Enthalpy of Vapori- Temperature (Enzation [Jmol-1] thalpy of Vaporization) [°C] 27600

25

References

Kiselev, V. D.; Veisman, E. A.; Zabotina, O. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 53; nb. 2; (1983); p. 333 - 342,289 - 297, View in Reaxys Svoboda et al.; Collection of Czechoslovak Chemical Communications; vol. 42; (1977); p.

1755,1756,1757,1759, View in Reaxys

27606.8

10

Smits; Cannegieter; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 168; (1934); p. 410, View in Reaxys

27538.4

32.8

Kolossowski; Alimow; Bulletin de la Societe Chimique de France; vol. <5>1; (1934); p. 878, View in Reaxys

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27319.4

38.4

Tyrer; Journal of the Chemical Society; vol. 101; (1912); p. 85, View in Reaxys

Further Information (69) Description (FurReferences ther Information) Further information Srinivasan et al.; Indian Journal of Physics, B; vol. 52; (1978); p. 24,31, View in Reaxys Further information Hertz; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 109; (1978); p. 9, View in Reaxys Further information Gibson; Canadian Journal of Chemistry; vol. 55; (1977); p. 2637,2638, View in Reaxys Further information Sundberg; Journal of Chemical Physics; vol. 66; (1977); p. 1475, View in Reaxys Further information Tachiya; Journal of Chemical Physics; vol. 66; (1977); p. 2282, View in Reaxys Further information Strong; Kaye; Journal of the American Chemical Society; vol. 98; (1976); p. 5460,5461, View in Reaxys Further information Huettermann et al.; Molecular Physics; vol. 32; (1976); p. 269,270, View in Reaxys Further information Dellepiane et al.; Spectroscopy Letters; vol. 9; (1976); p. 881, View in Reaxys Further information Funabashi; Magee; Journal of Chemical Physics; vol. 62; (1975); p. 4428, View in Reaxys Further information Evans; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 31; (1975); p. 609, View in Reaxys Further information Ambrose et al.; Journal of Applied Chemistry and Biotechnology; vol. 24; (1974); p. 359,369, View in Reaxys Further information Suzuki et al.; Journal of Molecular Spectroscopy; vol. 47; (1973); p. 118,121, View in Reaxys Further information Raetzsch; Freydank; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 253; (1973); p. 393,396, View in Reaxys Further information Kokurin; Vinogradov; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 461,484, View in Reaxys Further information Strat et al.; Journal of Applied Spectroscopy; vol. 18; (1973); p. 198; ; p. 263, View in Reaxys Further information Brosseau et al.; Journal of the American Chemical Society; vol. 94; (1972); p. 716, View in Reaxys Further information Dakhis; Dashevskii; Doklady Physical Chemistry; vol. 203; (1972); p. 201, View in Reaxys Further information DULLIEN FAL; AIChE Journal; vol. 18; nb. 1; (1972); p. 62 - 70, 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 Edge; Grant; Chemical Engineering Science; vol. 26; (1971); p. 1001,1005, View in Reaxys Further information Johnstone et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 5; (1970); p. 241, View in Reaxys Further information Missenard; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 270; (1970); p. 381, View in Reaxys Further information Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 17; (1969); p. 2049,2050, View in Reaxys Further information Murphy et al.; Applied Spectroscopy; vol. 23; (1969); p. 211,215, View in Reaxys Further information Clement; Malaval; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1161,1165, View in Reaxys Further information Fischer; Journal of Physical Chemistry; vol. 73; (1969); p. 3834, View in Reaxys Further information Charton; Charton; Journal of Organic Chemistry; vol. 34; (1969); p. 1882, View in Reaxys Further information Laurent et al.; Bulletin de la Societe Chimique de France; (1969); p. 70, View in Reaxys Further information Gray et al.; Journal of Chemical Physics; vol. 48; (1968); p. 1145,1148, View in Reaxys Further information Terrier; Weil; Berichte der Bunsen-Gesellschaft; vol. 72; (1968); p. 548, View in Reaxys Further information Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 2120, View in Reaxys Further information Hansch et al.; Journal of Organic Chemistry; vol. 33; (1968); p. 347, View in Reaxys Further information Franklin et al.; Journal of Chemical Physics; vol. 47; (1967); p. 3148,3152, View in Reaxys Further information Ivekovic; Gertner; Croatica Chemica Acta; vol. 39; (1967); p. 103,105, View in Reaxys Further information Dellepiane; Zerbi; Journal of Molecular Spectroscopy; vol. 24; (1967); p. 62,69, View in Reaxys Further information Lal; Indian Journal of Physics (1926-1976); vol. 41; (1967); p. 39,42, 43, View in Reaxys Further information Ache; Wolf; Journal of the American Chemical Society; vol. 88; (1966); p. 888,890,892, View in Reaxys

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Further information Meschkowa et al.; Russian Journal of Physical Chemistry; vol. 40; (1966); p. 925; Zhurnal Fizicheskoi Khimii; vol. 40; (1966); p. 1708, View in Reaxys Further information Barriol; Weissbecker; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 62; (1965); p. 623, View in Reaxys Further information Adema; Schrama; Analytical Chemistry; vol. 37; (1965); p. 229,230, View in Reaxys Further information Hudgens; Pish; Analytical Chemistry; vol. 37; (1965); p. 414, View in Reaxys Further information Venart; Journal of Chemical and Engineering Data; vol. 10; (1965); p. 239, View in Reaxys Further information Schnell; Monatshefte fuer Chemie; vol. 96; (1965); p. 1302,1305, View in Reaxys Further information Bolotnikova; Sichkar; Journal of Applied Spectroscopy; vol. 9; (1965); p. 1003; ; p. 500, View in Reaxys Further information Clement; Bothorel; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 61; (1964); p. 878,880, View in Reaxys Further information Jones et al.; Spectrochimica Acta; vol. 20; (1964); p. 1697,1700, View in Reaxys Further information Rice; Bald; Spectrochimica Acta; vol. 20; (1964); p. 721, View in Reaxys Further information Martin; Martin; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 1048, View in Reaxys Further information Lee; Journal of Physical Chemistry; vol. 67; (1963); p. 360,363, View in Reaxys Further information Dullien; Transactions of the Faraday Society; vol. 59; (1963); p. 856,862, View in Reaxys Further information Odum et al.; Journal of the American Chemical Society; vol. 85; (1963); p. 1050,1051, View in Reaxys Further information Schwetlick et al.; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 113,119, View in Reaxys Further information Vuks; Chernyavskaya; Sov. Phys. Dokl. (Engl. Transl.); vol. 7; (1963); p. 549,636, View in Reaxys Further information Beroza; Analytical Chemistry; vol. 34; (1962); p. 1801,1802, View in Reaxys Further information Petersen; Finkelstein; Journal of the American Chemical Society; vol. 84; (1962); p. 2222, 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 Li; Rossini; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 268, View in Reaxys Further information Baudet; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 58; (1961); p. 228,235, View in Reaxys Further information Elleman et al.; Journal of Molecular Spectroscopy; vol. 7; (1961); p. 322,335, View in Reaxys Further information Sinha; Jalaluddin; Indian Journal of Physics (1926-1976); vol. 35; (1961); p. 311,316, View in Reaxys Further information Gallais,F.; Voigt,D.; Bulletin de la Societe Chimique de France; (1960); p. 70 - 83, View in Reaxys Further information Bavin; Analytical Chemistry; vol. 32; (1960); p. 554, View in Reaxys Further information Fukui et al.; Bulletin of the Chemical Society of Japan; vol. 33; (1960); p. 1197,1200, View in Reaxys Further information Smith; Mortensen; Journal of Chemical Physics; vol. 32; (1960); p. 508,510, View in Reaxys Further information Dannley; Kitko; Analytical Chemistry; vol. 32; (1960); p. 1682, View in Reaxys Further information Higasi et al.; Journal of Physical Chemistry; vol. 64; (1960); p. 880,882, View in Reaxys Further information Walkley; Journal of Chemical Physics; vol. 33; (1960); p. 621, View in Reaxys Further information Bardamowa; Izvestiya Sibirskogo Otdeleniya Akademii Nauk SSSR, Seriya Khimicheskikh Nauk; vol. 2; (1960); p.

71,73, View in Reaxys Further information Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p. 207, View in Reaxys Heat Capacity Cp (2) Heat Capacity Cp Temperature (Heat [Jmol-1K-1] Capacity Cp) [°C]

References

104.07 - 107.42

-4 - 26

Chorazewski, Miroslaw; Goralski, Pawel; Tkaczyk, Mariola; Journal of Chemical and Engineering Data; vol. 50; nb. 2; (2005); p. 619 - 624, View in Reaxys

132.31

25

Tschamler; Richter; Wettig; Monatshefte fuer Chemie; vol. 80; (1949); p. 857, View in Reaxys

Interatomic Distances and Angles (3)

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Description

Comment (Interatomic Distances and Angles)

Interatomic distances and angles

References

Wagner; Dailey; Journal of Chemical Physics; vol. 26; (1957); p. 1588,1589,1591, View in Reaxys; Flanagan; Pierce; Journal of Chemical Physics; vol. 38; (1963); p. 2963,2964, View in Reaxys; Hayashi, Michiro; Fujitake, Masaharu; Inagusa, Tohihiro; Miyazaki, Sonoko; Journal of Molecular Structure; vol. 216; (1990); p. 9 - 26, View in Reaxys; Mager, T.; Schultz, E.; Bertagnolli, H.; Frahm, R.; Berichte der Bunsen-Gesellschaft; vol. 94; nb. 6; (1990); p. 703 - 709, View in Reaxys; Bertagnolli, H.; Schulz, G.; Berichte der Bunsen-Gesellschaft; vol. 90; (1986); p. 816 - 823, View in Reaxys

Interatomic distances and angles

C-C-Br: 109grad (Elektronenbeugung).

Beach; Stevenson; Journal of the American Chemical Society; vol. 61; (1939); p. 2645,2650, View in Reaxys

Interatomic distances and angles

C-Br: 1.91 bzw.

2.81 Angstroem (Elektronenbeugung).

Beach; Stevenson; Journal of the American Chemical Society; vol. 61; (1939); p. 2645,2650, View in Reaxys; Bru; Anales de la Real Sociedad Espanola de Fisica y Quimica; vol. 31; p. 118; Chem. Zentralbl.; vol. 104; nb. I; (1933); p. 2778, View in Reaxys

Ionization Potential (5) Ionization Potential Method (Ionization [eV] Potential)

Comment (Ionization Potential)

References

10.28

Photoionization

Type: vertical

Alfassi, Zeev B.; Huie, Robert E.; Mittal, Jai P.; Neta, P.; Shoute, Lian C. T.; Journal of Physical Chemistry; vol. 97; nb. 36; (1993); p. 9120 - 9123, View in Reaxys

10.3

PE

Type: vertical.

Higher potentials: 10.60 eV

Ohno, Koichi; Imai, Keitaro; Harada, Yoshiya; Journal of the American Chemical Society; vol. 107; nb. 26; (1985); p. 8078 - 8082, View in Reaxys

10.28

Photoionization

Type: vertical.

Higher potentials: 10.60eV

Hoppilliard, Y.; Solgadi, D.; Tetrahedron; vol. 36; nb. 3; (1980); p. 377 380, View in Reaxys

10.29

PE

Type: vertical.

Utsunomiya, Chikatoshi; Kobayashi, Tsunetoshi; Nagakura, Saburo; Higher potentials: Bulletin of the Chemical Society of Japan; vol. 53; nb. 5; (1980); p. 1216 10.60, 12.47, 13.11, 1220, View in Reaxys 14.17, 15.33, 16.26 Morrison; Nicholson; Journal of Chemical Physics; vol. 20; (1952); p.

1021, View in Reaxys; Irsa; Journal of Chemical Physics; vol. 26; (1957); p. 18,19, View in Reaxys; Watanabe; Journal of Chemical Physics; vol. 26; (1957); p. 542,543; Journal of Chemical Physics; vol. 22; (1954); p.

1564,1566, View in Reaxys; Gibson; Canadian Journal of Chemistry; vol.

55; (1977); p. 2637,2638, View in Reaxys; Johnstone et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 5; (1970); p. 241, View in Reaxys; Litvak et al.; Chemical Physics Letters; vol. 36; (1975); p.

145,148, View in Reaxys; Brogli; Heilbronner; Helvetica Chimica Acta; vol. 54; (1971); p. 1423,1425, 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; Kimura et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 373,374, View in Reaxys; Hashmall; Heilbronner; Angewandte Chemie; vol. 82; (1970); p. 320, View in Reaxys; Gruetzmacher; Organic Mass Spectrometry; vol. 3; (1970); p. 131,134, View in Reaxys; Poldoja; Palm; Organic Reactivity (New York, English Translation); vol. 4; (1967); p. 320,329, View in Reaxys; Charton; Charton; Journal of Organic Chemistry; vol. 34; (1969); p. 1882, View in Reaxys

Liquid Phase (3) Description (Liquid References Phase) Association in the liquid state

Mc Clellan; Nicksic; Journal of Physical Chemistry; vol. 69; (1965); p. 446, View in Reaxys

Self-association in solution

Mc Clellan; Nicksic; Journal of Physical Chemistry; vol. 69; (1965); p. 446, View in Reaxys

Rate of evaporation

Vaillant; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 150; (1910); p. 215,689,1048, View in Reaxys; Smits; Cannegieter; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik,

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Kinetik, Elektrochemie, Eigenschaftslehre; vol. 172; (1935); p. 14, View in Reaxys; Smith; Journal of the Chemical Society; (1931); p. 2578,2580, View in Reaxys Liquid/Liquid Systems (MCS) (11) 1 of 11

Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) 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 2 of 11

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 3 of 11

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 4 of 11

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

24.9

Partner (Liquid/Liquid Systems (MCS))

1.) water; 2.) micellar solution of Na dodecyl sulfate

Suslov; Solomonov; Russian Journal of Physical Chemistry A; vol. 72; nb. 5; (1998); p. 831 - 835, View in Reaxys 5 of 11

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 6 of 11

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

Leahy; Journal of pharmaceutical sciences; vol. 75; nb. 7; (1986); p. 629 - 636, View in Reaxys

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Description (Liquid/Liquid Distribution between solvent 1 + 2 Systems (MCS)) Rekker; Kort; European Journal of Medicinal Chemistry; vol. 14; (1979); p. 479,484, View in Reaxys; Hansch et al.; Journal of Medicinal Chemistry; vol. 18; (1975); p. 546,547, View in Reaxys

8 of 11

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))

aliphatic acid

Kolossowsky; Kulikow; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 64; Chem. Zentralbl.; vol. 107; nb. II; (1936); p.

1511,2880, View in Reaxys; Kolossowsky; Kulikow; Zeitschrift fuer Physikalische Chemie, Abteilung A: Chemische Thermodynamik, Kinetik, Elektrochemie, Eigenschaftslehre; vol. 169; (1934); p. 462; Zhurnal Obshchei Khimii; vol. 4; (1934); p.

1096,1374; Chem. Zentralbl.; vol. 106; nb. I; (1935); p. 1037, View in Reaxys; Kolossowski; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 1047; Chem. Zentralbl.; vol. 107; nb. I; (1936); p. 3485, View in Reaxys; Kolossowski; Bekturow; Kulikow; Zhurnal Obshchei Khimii; vol. 4; (1934); p. 1227; Zhurnal Obshchei Khimii; vol. 5; (1935); p. 322; Chem. Zentralbl.; vol. 107; nb. I; (1936); p. 2727,4420, View in Reaxys 9 of 11

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0

Partner (Liquid/Liquid Systems (MCS))

water; methanol

Bonner; Journal of Physical Chemistry; vol. 14; (1910); p. 755, View in Reaxys 10 of 11

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0

Partner (Liquid/Liquid Systems (MCS))

water; ethanol

Bonner; Journal of Physical Chemistry; vol. 14; (1910); p. 755, View in Reaxys 11 of 11

Description (Liquid/Liquid Liquid/liquid phase diagram Systems (MCS)) Temperature (Liquid/ Liquid Systems (MCS)) [°C]

0

Partner (Liquid/Liquid Systems (MCS))

water; propan-1-ol

Bonner; Journal of Physical Chemistry; vol. 14; (1910); p. 755, View in Reaxys Liquid/Solid Systems (MCS) (1) 1 of 1

Description (Liquid/Solid Systems (MCS))

Solidification diagram

Comment (Liquid/Solid Systems (MCS))

Verbindung 1:1.

Partner (Liquid/Solid Systems (MCS))

aluminium bromide

Burbage; Garrett; Journal of Physical Chemistry; vol. 56; (1952); p. 730, View in Reaxys Liquid/Vapour Systems (MCS) (56)

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1 of 56

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))

water

Li, Jianjun; Dallas, Andrew J.; Eikens, David I.; Carr, Peter W.; Bergmann, Diane L.; Hait, Mitchell J.; Eckert, Charles A.; Analytical Chemistry; vol. 65; nb. 22; (1993); p. 3212 - 3218, View in Reaxys 2 of 56

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 3 of 56

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 4 of 56

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 5 of 56

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 6 of 56

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))

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

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7 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

acetonitrile

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 8 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

acetophenone

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 9 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

aniline

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 10 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

methoxybenzene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 11 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

benzene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 12 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

benzonitrile

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 13 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

Benzyl acetate

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 14 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

benzyl chloride

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 15 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

butan-1-ol

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Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 16 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

butanone

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 17 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 18 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

cyclohexanone

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 19 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

1,2-dichloro-ethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 20 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

N,N-dimethyl-formamide

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 21 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 22 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

ethanol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 23 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

n-heptane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 24 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

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Partner (Liquid/Vapour Systems (MCS))

2,2,4-trimethylpentane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 25 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

nitrobenzene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 26 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

Nitroethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 27 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

nitromethane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 28 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

2-nitropropane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 29 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

octane

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 30 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

octanol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 31 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

phenol

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 32 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

propiononitrile

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys

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33 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

1-phenyl-propan-1-one

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 34 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

quinoline

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 35 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

toluene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 36 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

para-xylene

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 37 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

n-Butyl chloride

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 38 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

Partner (Liquid/Vapour Systems (MCS))

H2O

Thomas, Eugene R.; Newman, Bruce A.; Long, Thomas C.; Wood, Douglas A.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 4; (1982); p. 399 - 405, View in Reaxys 39 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

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

41.6 - 60.1

Partner (Liquid/Vapour Systems (MCS))

butanone

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 40 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

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

27.9 - 67.1

Partner (Liquid/Vapour Systems (MCS))

hexane

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Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 41 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

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

75.6

Partner (Liquid/Vapour Systems (MCS))

triethylamine

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 42 of 56

Description (Liquid/ Vapour Systems (MCS))

Activity coefficients of the components in the mixture

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

31.9 - 49.9

Partner (Liquid/Vapour Systems (MCS))

methylene chloride

Thomas, Eugene R.; Newman, Bruce A.; Nicolaides, George L.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 27; nb. 3; (1982); p. 233 - 240, View in Reaxys 43 of 56

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 44 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Bittrich; Werner; Wissenschaftliche Zeitschrift der Technischen Hochschule "Carl Schorlemmer" Leuna-Merseburg; vol. 7; (1965); p. 247,251, View in Reaxys 45 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

25

Partner (Liquid/Vapour Systems (MCS))

aluminium bromide

Van Dyke; Journal of the American Chemical Society; vol. 72; (1950); p. 3619,3620, View in Reaxys 46 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

-45.8

Partner (Liquid/Vapour Systems (MCS))

aluminium bromide

Brown; Wallace; Journal of the American Chemical Society; vol. 75; (1935); p. 6279,6282, View in Reaxys 47 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

-31.3

Partner (Liquid/Vapour Systems (MCS))

aluminium bromide

Brown; Wallace; Journal of the American Chemical Society; vol. 75; (1935); p. 6279,6282, View in Reaxys 48 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

0

Partner (Liquid/Vapour Systems (MCS))

aluminium bromide

Brown; Wallace; Journal of the American Chemical Society; vol. 75; (1935); p. 6279,6282, View in Reaxys 49 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

50

Partner (Liquid/Vapour Systems (MCS))

n-heptane

Smyth; Engel; Journal of the American Chemical Society; vol. 51; (1929); p. 2649, View in Reaxys 50 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

30

Partner (Liquid/Vapour Systems (MCS))

ethanol

Smyth; Engel; Journal of the American Chemical Society; vol. 51; (1929); p. 2649, View in Reaxys 51 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

0.3

Partner (Liquid/Vapour Systems (MCS))

2-butanol

Roland; Bulletin des Societes Chimiques Belges; vol. 37; (1928); p. 122; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 2900, View in Reaxys 52 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

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

16.8

Partner (Liquid/Vapour Systems (MCS))

2-butanol

Roland; Bulletin des Societes Chimiques Belges; vol. 37; (1928); p. 122; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 2900, View in Reaxys 53 of 56

Description (Liquid/ Vapour Systems (MCS))

Boiling points of mixtures

Partner (Liquid/Vapour Systems (MCS))

ethanol

Paul; Schantz; Archiv der Pharmazie (Weinheim, Germany); vol. 257; (1919); p. 105, View in Reaxys 54 of 56

Description (Liquid/ Vapour Systems (MCS))

Boiling points of mixtures

Partner (Liquid/Vapour Systems (MCS))

water

Paul; Schantz; Archiv der Pharmazie (Weinheim, Germany); vol. 257; (1919); p. 105, View in Reaxys 55 of 56

Description (Liquid/ Vapour Systems (MCS))

Boiling points of mixtures

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Partner (Liquid/Vapour Systems (MCS))

water; ethanol

Paul; Schantz; Archiv der Pharmazie (Weinheim, Germany); vol. 257; (1919); p. 105, View in Reaxys 56 of 56

Description (Liquid/ Vapour Systems (MCS))

Vapour pressure diagram for the mixture

Pressure (Liquid/Vapour Systems (MCS)) [Torr]

760

Comment (Liquid/Vapour Systems (MCS))

Zusammensetzung des Dampfes.

Partner (Liquid/Vapour Systems (MCS))

benzene

Tyrer; Journal of the Chemical Society; vol. 101; (1912); p. 85, View in Reaxys Magnetic Data (1) Description (Magnetic Data)

References

Anisotropy of mag- Vul'fson, S.G.; Dianova, O.M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (Engnetic susceptibility lish Translation); vol. 33; nb. 10; (1984); p. 2070 - 2074; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb.

10; (1984); p. 2269 - 2274, View in Reaxys Magnetic Susceptibility (1) References Pascal; Bulletin de la Societe Chimique de France; vol. <4>7; (1910); p. 49; Bulletin de la Societe Chimique de France; vol. <4>11; (1912); p.

161, View in Reaxys; Pascal; Annales de Chimie (Cachan, France); vol. <8>19; (1910); p. 28,40; Bulletin de la Societe Chimique de France; vol. <4>11; (1912); p. 116, View in Reaxys; Bernstein; Journal of Physical Chemistry; vol. 69; (1965); p. 1550,1558, View in Reaxys; Baudet; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 58; (1961); p. 228,235, View in Reaxys Mechanical & Physical Properties (MCS) (5) 1 of 5

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

25

Partner (Mechanical & Physical Properties (MCS))

1-iodo-butane

Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 6; (1994); p. 609 - 616, View in Reaxys 2 of 5

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

25

Partner (Mechanical & Physical Properties (MCS))

methyl iodide

Artal, M.; Embid, J. Munoz; Velasco, I.; Journal of Chemical Thermodynamics; vol. 26; nb. 7; (1994); p. 703 - 708, View in Reaxys 3 of 5

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

25

Partner (Mechanical & Physical Properties (MCS))

benzene

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Gallardo, M. A.; Vicente, I. Garcia; Velasco, I.; Otin, S.; Journal of Chemical Thermodynamics; vol. 21; nb. 10; (1989); p.

1101 - 1104, View in Reaxys 4 of 5

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

Terasawa et al.; Journal of Physical Chemistry; vol. 79; (1975); p. 2345,2346-2351, View in Reaxys 5 of 5

Description (Mechanical & Physical Properties (MCS))

Virial coefficients

Raetzsch; Bittrich; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 228; (1965); p. 81, View in Reaxys Mechanical Properties (7) Description (MeComment (MeReferences chanical Properties) chanical Properties) Molar volume

Bernstein; Journal of Physical Chemistry; vol. 69; (1965); p. 1550,1558, View in Reaxys; Berrebi; Decroocq; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 71; (1974); p.

673,678, View in Reaxys; Abraham; Johnston; Journal of the Chemical Society [Section] A: Inorganic, Physical, Theoretical; (1971); p. 1610,1611, View in Reaxys; Bulgarevich; Burdastykh; Boiko; Russian Journal of General Chemistry; vol. 77; nb. 7; (2007); p. 1244 - 1253, View in Reaxys

PVT Relationship

Kumagai; Iwasaki; Journal of Chemical and Engineering Data; vol. 23; (1978); p. 193,194, View in Reaxys

Virial coefficients of the equation of state

Raetzsch; Bittrich; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 228; (1965); p. 81, View in Reaxys; Edwards; Puebla; Berichte der Bunsen-Gesellschaft; vol. 80; (1976); p. 350, View in Reaxys

Viscosity

Bytenskii; J. Appl. Chem. USSR (Engl. Transl.); vol. 45; (1972); p. 453,458, View in Reaxys; Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p. 207, View in Reaxys; Flood; Bartholomew; Canadian Journal of Chemistry; vol. 46; (1968); p. 249,253, View in Reaxys; Gorenbein; Smolenzew; Ukrainskii Khimicheskii Zhurnal (Russian Edition); vol. 28; (1962); p. 185, View in Reaxys; Kotisek; Marek; Chemicky Prumysl; vol. 5; (1955); p.

330,331, 332; Chem.Abstr.; nb. 6239; (1960), View in Reaxys; Vilim; Rezabek; Chemicky Prumysl; vol. 10; (1960); p. 533, View in Reaxys

Volume change on melting

Zhokhovskii; Russian Journal of Physical Chemistry; vol. 37; (1963); p. 1428; Zhurnal Fizicheskoi Khimii; vol. 37; (1963); p. 2635, View in Reaxys

Compressibility

Mayer; Journal of Physical Chemistry; vol. 67; (1963); p. 2160,2161, View in Reaxys

Internal pressure

Binnendruck.

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol.

65; (1909); p. 134; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 395,427, View in Reaxys

Molecular Deformation (2) Description (MoReferences lecular Deformation) Force constants

Melendez-Andreu; Annales de Chimie (Cachan, France); vol. 7; nb. 13; (1962); p. 695,702, View in Reaxys; Chalk, Christine D.; Hutley, Barrie G.; McKenna, James; Sims, Leslie B.; Williams, Ian H.; Journal of the American Chemical Society; vol. 103; nb. 2; (1981); p. 260 - 268, View in Reaxys; McKenna, James; Sims, Leslie B.; Williams, Ian H.; Journal of the American Chemical Society; vol. 103; nb. 2; (1981); p. 268 - 272, View in Reaxys

Fundamental vibra- Takenaka; Nippon Kagaku Zasshi; vol. 82; (1961); p. 1309,1312; Chem.Abstr.; vol. 57; nb. 1569; (1962), tions View in Reaxys Optics (9) Description (Optics)

Comment (Optics)

References

Magnetic birefringence (CottonMouton effect)

Le Fevre et al.; Australian Journal of Chemistry; vol. 24; (1971); p. 1177,1180, View in Reaxys; Vul'fson, S.G.; Dianova, O.M.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; nb. 10; (1984); p. 2070 - 2074; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 10; (1984); p. 2269 - 2274, View in Reaxys

Electric birefringence (Kerr effect)

Le Fevre; Williams; Journal of the Chemical Society; (1965); p. 4185, View in Reaxys; Khanarian, G.; Tonelli, A. E.; Journal of Chemical Physics; vol. 75; nb. 10; (1981); p. 5031 - 5036, View in Reaxys

Magnetorotation

Murthy; Naidu; Current Science; vol. 48; (1979); p. 292, View in Reaxys

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Rayleigh scattering

Pinnow et al.; Journal of Chemical Physics; vol. 49; (1968); p. 347,354, View in Reaxys

Diffraction

Clement; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 255; (1962); p. 863, View in Reaxys; Vincent-Geisse; Journal de Physique (Paris); vol. 26; (1965); p.

289,292, View in Reaxys

Magnetorotation

β:578 nm.

Voigt; Gallais; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol.

246; (1958); p. 2892,2894, View in Reaxys

Magnetorotation

von Gemischen mit Jodaethan.

Fleming; Saunders; Journal of the Chemical Society; (1955); p. 4147,4148, View in Reaxys

Magnetorotation

in dampffoermigem de Mallemann; Gabiano; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciund fluessigem Ae- ences; vol. 192; (1931); p. 279, View in Reaxys; Gabiano; Annales de Physique (Paris, France); thylbromid. vol. <10>20; (1933); p. 100, View in Reaxys

Degree of depolarization of Rayleigh scattering

bei der molekularen Rao; Indian J.Phys.; vol. 2; p. 82; Chem. Zentralbl.; vol. 99; nb. I; (1928); p. 1838, Lichtzerstreuung View in Reaxys; Ramanathan; Srinivasan; Chem. Zentralbl.; vol. 97; nb. II; (1926); p. 1930, des dampffoermiView in Reaxys gen Aethylbromids.

Other Thermochemical Data (5) Description (Other Comment (Other Thermochemical Thermochemical Data) Data)

References

Entropy

Murai; Kimura; Nippon Kagaku Kaishi; (1972); p. 2096,2097, View in Reaxys; Samuels; Espenson; Inorganic Chemistry; vol. 18; (1979); p. 2587,2588, View in Reaxys; Chalk, Christine D.; Hutley, Barrie G.; McKenna, James; Sims, Leslie B.; Williams, Ian H.; Journal of the American Chemical Society; vol. 103; nb. 2; (1981); p. 260 - 268, View in Reaxys

Enthalpy

Samuels; Espenson; Inorganic Chemistry; vol. 18; (1979); p. 2587,2588, View in Reaxys

Thermodynamic properties

Murai; Kimura; Nippon Kagaku Kaishi; (1972); p. 2096,2097, View in Reaxys; Green; Holden; Journal of the Chemical Society; (1962); p. 1794, View in Reaxys; Kimura et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 373,374, View in Reaxys

Ebullioscopic constant

Molakulare Siedepunktserhoehung:27.9.

Heat of combustion fuer Aethylbromidat constant volume Dampf:328.4 kcal/ Mol.

Beckmann; Fuchs; Gernhardt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 18; (1895); p. 511, View in Reaxys Berthelot; Annales de Chimie (Cachan, France); vol. <5> 23; (1881); p. 209, View in Reaxys

Partition octan-1-ol/water (MCS) (1) 1 of 1

log POW

1.87

Temperature (Partition octan-1-ol/water (MCS)) [°C]

25

Ruelle, Paul; Kesselring, Ulrich W.; Journal of Pharmaceutical Sciences; vol. 87; nb. 8; (1998); p. 1015 - 1024, View in Reaxys Self-diffusion (5) Temperature (Selfdiffusion) [°C]

References

7.4

Stein; Carman; J.S.African chem.Inst.<N.S.>; vol. 9; (1955); p. 55,58, View in Reaxys

19.3

Stein; Carman; J.S.African chem.Inst.<N.S.>; vol. 9; (1955); p. 55,58, View in Reaxys

30

Stein; Carman; J.S.African chem.Inst.<N.S.>; vol. 9; (1955); p. 55,58, View in Reaxys; Graupner; Winter; Journal of the Chemical Society; (1952); p. 1145,1146, View in Reaxys

15

Graupner; Winter; Journal of the Chemical Society; (1952); p. 1145,1146, View in Reaxys

22.5

Graupner; Winter; Journal of the Chemical Society; (1952); p. 1145,1146, View in Reaxys

Solubility (MCS) (12) 1 of 12

Solubility [g·l-1]

9.1

Solvent (Solubility (MCS))

water

Location

Paragraph 0041

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Patent; SAJET DEVELOPMENT LLC; MILLER, Jorge; KLING MILLER, Luisa; WO2013/119230; (2013); (A1) English, View in Reaxys 2 of 12

Saturation

in pure solvent

Comment (Solubility (MCS))

equation

Jain, Neera; Yalkowsky, Samuel H.; Journal of Pharmaceutical Sciences; vol. 90; nb. 2; (2001); p. 234 - 252, View in Reaxys 3 of 12

Saturation

in pure solvent

Valvani; Yalkowsky; Roseman; Journal of Pharmaceutical Sciences; vol. 70; nb. 5; (1981); p. 502 - 507, View in Reaxys 4 of 12

Comment (Solubility (MCS))

in wss. Lsg. v. Polymeren, Fig. 1-6

Okubo et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 397, View in Reaxys 5 of 12

Comment (Solubility (MCS))

1,2,4-Trichlorbenzol (auch in Ggw. von GaBr3 S.3150)

Kwun; Choi; Journal of Physical Chemistry; vol. 72; (1968); p. 3148, View in Reaxys 6 of 12

Comment (Solubility (MCS))

Nitrobenzol (auch in Ggw. von GaBr3 S.3150)

Kwun; Choi; Journal of Physical Chemistry; vol. 72; (1968); p. 3148, View in Reaxys 7 of 12

Temperature (Solubility (MCS)) [°C]

30

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

100 g solvent dissolves. 0.0082 Mol Substance.

van Arkel; Vles; Recueil des Travaux Chimiques des Pays-Bas; vol. 55; (1936); p. 408, View in Reaxys 8 of 12

Solubility [g·l-1]

9.52

Saturation

in solution

Temperature (Solubility (MCS)) [°C]

17.5

Solvent (Solubility (MCS))

H2O

Fuehner; Chemische Berichte; vol. 57; (1924); p. 514; Biochemische Zeitschrift; vol. 115; (1921); p. 260, View in Reaxys 9 of 12

Temperature (Solubility (MCS)) [°C]

0

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

100 g solvent dissolves. 1.067 g Substance.

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys 10 of 12

Temperature (Solubility (MCS)) [°C]

10

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

100 g solvent dissolves. 0.965 g Substance.

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys 11 of 12

Temperature (Solubility (MCS)) [°C]

20

Solvent (Solubility (MCS))

H2O

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Comment (Solubility (MCS))

100 g solvent dissolves. 0.914 g Substance.

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys 12 of 12

Temperature (Solubility (MCS)) [°C]

30

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

100 g solvent dissolves. 0.896 g Substance.

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys Solution Behaviour (MCS) (13) 1 of 13

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

sodium deoxycholate

Ascone, I.; D'Angelo, P.; Pavel, N. V.; Journal of Physical Chemistry; vol. 98; nb. 11; (1994); p. 2982 - 2990, View in Reaxys 2 of 13

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

rubidium deoxycholate

Ascone, I.; D'Angelo, P.; Pavel, N. V.; Journal of Physical Chemistry; vol. 98; nb. 11; (1994); p. 2982 - 2990, View in Reaxys 3 of 13

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

hexane

Ascone, I.; D'Angelo, P.; Pavel, N. V.; Journal of Physical Chemistry; vol. 98; nb. 11; (1994); p. 2982 - 2990, View in Reaxys 4 of 13

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

sodium dodecyl-sulfate

Ascone, I.; D'Angelo, P.; Pavel, N. V.; Journal of Physical Chemistry; vol. 98; nb. 11; (1994); p. 2982 - 2990, View in Reaxys 5 of 13

Description (Solution Behaviour (MCS))

Solubilizing

Partner (Solution Behaviour (MCS))

H2O

Ascone, I.; D'Angelo, P.; Pavel, N. V.; Journal of Physical Chemistry; vol. 98; nb. 11; (1994); p. 2982 - 2990, View in Reaxys 6 of 13

Description (Solution Behaviour (MCS))

Dissolving capacity

Bezrukov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol.

20; (1971); p. 279,282; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 342, View in Reaxys; Gerrard; Journal of Applied Chemistry and Biotechnology; vol. 22; (1972); p. 623,628, View in Reaxys 7 of 13

Description (Solution Behaviour (MCS))

Miscibility

Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

water

Donahue; Bartell; Journal of Physical Chemistry; vol. 56; (1952); p. 480,483, View in Reaxys 8 of 13

Description (Solution Behaviour (MCS))

Dissolving capacity

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Temperature (Solution Be- 25 haviour (MCS)) [°C] Partner (Solution Behaviour (MCS))

water; H2O

Templeton; Hall; Journal of Physical Chemistry; vol. 51; (1947); p. 1444, View in Reaxys 9 of 13

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 25 haviour (MCS)) [°C] Pressure (Solution Behaviour (MCS)) [Torr]

256

Partner (Solution Behaviour (MCS))

acetylene

Gand; Bulletin de la Societe Chimique de France; vol. <5>12; (1945); p. 1058, View in Reaxys 10 of 13

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 20 haviour (MCS)) [°C] Pressure (Solution Behaviour (MCS)) [Torr]

760

Partner (Solution Behaviour (MCS))

hydrogenchloride

Bell; Journal of the Chemical Society; (1931); p. 1377, View in Reaxys 11 of 13

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Be- 20 haviour (MCS)) [°C] Pressure (Solution Behaviour (MCS)) [Torr]

760

Partner (Solution Behaviour (MCS))

hydrogen sulfide

Bell; Journal of the Chemical Society; (1931); p. 1377, View in Reaxys 12 of 13

Description (Solution Behaviour (MCS))

Miscibility

Partner (Solution Behaviour (MCS))

vanadium oxychloride

Brown; Snyder; Journal of the American Chemical Society; vol. 47; (1925); p. 2674, View in Reaxys 13 of 13

Description (Solution Behaviour (MCS))

Dissolving capacity

Partner (Solution Behaviour (MCS))

dithiocarbonic acid O-benzyl ester

v. Halban; Hecht; Zeitschrift fuer Elektrochemie und Angewandte Physikalische Chemie; vol. 24; (1918); p. 80, View in Reaxys Sound Properties (4) Description (Sound Comment (Sound Properties) Properties)

References

Ultrasonic properties

Solovyev et al.; Journal of Chemical Physics; vol. 48; (1968); p. 2155, View in Reaxys; Plass; Berichte der Bunsen-Gesellschaft; vol. 74; (1970); p. 343,344-346, View in Reaxys

Sound absorption

Fluessigkeit;bei 25grad.

Verma; Journal of Chemical Physics; vol. 18; (1950); p. 1352, View in Reaxys; Heasell; Lamb; Pr.phys.Soc.London<B>; vol. 69; (1956); p. 869,874, View in Reaxys

Velocity of sound

in Aethylbromid zwischen 0grad

Pellam; Galt; Journal of Chemical Physics; vol. 14; (1946); p. 612, View in Reaxys; 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,

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(968 m/sec) und View in Reaxys; Parthasarathy; Proceedings - Indian Academy of Sciences, Section A; vol. 3; p.

30grad (866 m/sec). 520; Chem. Zentralbl.; vol. 107; nb. II; (1936); p. 2083, View in Reaxys; Swanson; Journal of Chemical Physics; vol. 2; (1934); p. 689,690, View in Reaxys Velocity of sound

in Aethylbromid unter Drucken zwischen 179 und 216 atm bei 24.7grad.

Swanson; Hubbard; Physical Review; vol. <2> 45; (1934); p. 291, View in Reaxys; Swanson; Journal of Chemical Physics; vol. 2; (1934); p. 689,690, View in Reaxys

Static Dielectric Constant (5) Static Dielectric Temperature (Static References Constant Dielectric Constant) [°C] Decroocq; Bulletin de la Societe Chimique de France; (1964); p. 127,133, View in Reaxys 9.4

20

Timmermans et al.; Bulletin des Societes Chimiques Belges; vol. 64; (1955); p. 5,19, View in Reaxys

9.5

20

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

9.2

25

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2071,2072, View in Reaxys

10.23

1

Heston et al.; Journal of the American Chemical Society; vol. 72; (1950); p. 2071,2072, View in Reaxys

Surface Tension (9) Surface Tension Temperature (Sur[g·s-2] face Tension) [°C]

References Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol.

65; (1909); p. 134; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 395,427, View in Reaxys; Richards; Mathews; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 61; (1908); p. 452; Journal of the American Chemical Society; vol. 30; (1908); p. 10, View in Reaxys; Dow Chem. Co. bei Dreisbach; Advances in Chemistry Series; (1959); p. 207, View in Reaxys; Mayer; Journal of Physical Chemistry; vol. 67; (1963); p. 2160,2161, View in Reaxys

24.1

20

Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys

23.45

25

Mumford; Phillips; Journal of the Chemical Society; (1950); p. 75,78, View in Reaxys

23.3 - 24.32

16.9 - 25.2

Vogel; Journal of the Chemical Society; (1943); p. 643, View in Reaxys

25.26

10

Radulescu; Kolloid-Zeitschrift; vol. 87; (1939); p. 282, View in Reaxys

24.83

15

Hennaut-Roland; Lek; Bulletin des Societes Chimiques Belges; vol. 40; (1931); p. 183, View in Reaxys

24.15

20

Hennaut-Roland; Lek; Bulletin des Societes Chimiques Belges; vol. 40; (1931); p. 183, View in Reaxys

22.83

30

Hennaut-Roland; Lek; Bulletin des Societes Chimiques Belges; vol. 40; (1931); p. 183, View in Reaxys

24.16

20

Harkins; Clark; Roberts; Journal of the American Chemical Society; vol. 42; (1920); p. 703, View in Reaxys

Transport Data (1) Description (Trans- References port Data) Thermal conductiv- Cecil; Munch; Industrial and Engineering Chemistry; vol. 48; (1956); p. 437,440, View in Reaxys; Bridgman; Proceedity ings of the National Academy of Sciences of the United States of America; vol. 9; p. 341; Chem. Zentralbl.; vol. 95; nb.

I; (1924); p. 539, View in Reaxys; Riedel; Mitt.Kaeltetechn,Inst.; nb. 2; (1948); p. 3,23, View in Reaxys; Missenard; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 270; (1970); p. 381, View in Reaxys; Edwards; Puebla; Berichte der Bunsen-Gesellschaft; vol. 80; (1976); p. 350, View in Reaxys Transport Phenomena (MCS) (6) 1 of 6

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

diethyl ether; benzene

Temperature (Transport Phenomena (MCS)) [°C]

3.85

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Partner (Transport Phenomena (MCS))

Mg

Maslennikov; Spirina; Russian Journal of General Chemistry; vol. 68; nb. 12; (1998); p. 1876 - 1877, View in Reaxys 2 of 6

Description (Transport Phenomena (MCS))

Diffusion

Lugg; Analytical Chemistry; vol. 40; (1968); p. 1072,1074, View in Reaxys; Lawson; Journal of Chemical Physics; vol. 32; (1960); p. 131, View in Reaxys; Lusis; Ratcliff; AIChE Journal; vol. 17; (1971); p. 1492,1493, View in Reaxys; Fuller et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 3679, View in Reaxys 3 of 6

Description (Transport Phenomena (MCS))

Diffusion

Comment (Transport Phenomena (MCS))

durch die Haut.

Schwander; Arch.Gewerbe-Path.; vol. 7; (1936); p. 114; Chem. Zentralbl.; vol. 110; nb. II; (1939); p. 1331, View in Reaxys 4 of 6

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

30

Pressure (Transport Phenomena (MCS)) [Torr]

900074

Bridgman; Proceedings of the National Academy of Sciences of the United States of America; vol. 11; p. 604; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 1923, View in Reaxys; Bridgman; Pr.am.Acad.Arts Sci.; vol. 61; (1925); p. 70,78; Chem.

Zentralbl.; vol. 100; nb. I; (1929); p. 1919, View in Reaxys 5 of 6

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport Phenomena (MCS)) [°C]

75

Pressure (Transport Phenomena (MCS)) [Torr]

900074

Bridgman; Proceedings of the National Academy of Sciences of the United States of America; vol. 11; p. 604; Chem. Zentralbl.; vol. 100; nb. II; (1929); p. 1923, View in Reaxys; Bridgman; Pr.am.Acad.Arts Sci.; vol. 61; (1925); p. 70,78; Chem.

Zentralbl.; vol. 100; nb. I; (1929); p. 1919, View in Reaxys 6 of 6

Description (Transport Phenomena (MCS))

Diffusion

Solvent (Transport Phenomena (MCS))

methanol

Comment (Transport Phenomena (MCS))

Diffusionsgeschwindigkeit.

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 Vapour Pressure (12) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C]

References Li; Rossini; Journal of Chemical and Engineering Data; vol. 6; (1961); p. 268, View in Reaxys

12.15 - 212.1

-45.6 - 5.8

Brown; Wallace; Journal of the American Chemical Society; vol. 75; (1953); p. 6279,6284, View in Reaxys

59 - 386

-20 - 20

Leitch; Morse; Canadian Journal of Chemistry; vol. 31; (1953); p. 785,788; Org.Synth.Isotopes; (1958); p. 1473, View in Reaxys

165 - 800

0 - 40

Neiman; Schuschunow; Zhurnal Fizicheskoi Khimii; vol. 22; p. 146; Chem.Abstr.; (1948); p.

5315, View in Reaxys

32

-30

Hansen; Annalen der Physik (Weinheim, Germany); vol. <5>35; (1939); p. 525, View in Reaxys

386

20

Hansen; Annalen der Physik (Weinheim, Germany); vol. <5>35; (1939); p. 525, View in Reaxys

564

30

Hansen; Annalen der Physik (Weinheim, Germany); vol. <5>35; (1939); p. 525, View in Reaxys

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165.8 - 315.2

0.3 - 15

Roland; Bulletin des Societes Chimiques Belges; vol. 37; (1928); p. 122; Chem. Zentralbl.; vol.

99; nb. I; (1928); p. 2900, View in Reaxys

165.2

0

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys; Regnault; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1860); p. 39; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1863); p. 67, View in Reaxys

256.9

10

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys; Regnault; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1860); p. 39; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1863); p. 67, View in Reaxys

385.9

20

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys; Regnault; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1860); p. 39; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1863); p. 67, View in Reaxys

563.7

30

Rex; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 55; (1906); p. 365, View in Reaxys; Regnault; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1860); p. 39; Jahresbericht ueber die Fortschritte der Chemie und Verwandter Theile Anderer Wissenschaften; (1863); p. 67, View in Reaxys

NMR Spectroscopy (44) 1 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400 scopy) [MHz] Original Text (NMR Spec- NMR (600 MHz) β 7.40 - 7.30 (comp, 5 H), 7.03 (s, 1 H), 6.79 (d, 7 = 10.1 Hz, 1 H), 6.65 (d, / = troscopy) 32.8 Hz, 1 H), 5.17 (s, 2 H), 4.61 (s, 2 H), 3.70 (s, 2 H), 3.19 (s, 4 H), 2.78 (s, 2 H), 2.62 (s, 4 H), 2.50 (q, / = 7.2 Hz, 2 H), 1.14 (t, / = 7.2 Hz, 3 H); Location

Paragraph 0194

Patent; BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM; MARTIN, Stephen, F.; SAHN, James, J.; LINKENS, Kathryn, Taylor; (119 pag.); WO2017/190109; (2017); (A1) English, View in Reaxys 2 of 44

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

chloroform-d1

Frequency (NMR Spectro- 400.1 scopy) [MHz] Location

supporting information

McKeever, Caitriona; Kaiser, Marcel; Rozas, Isabel; Journal of Medicinal Chemistry; vol. 56; nb. 3; (2013); p. 700 - 711, View in Reaxys 3 of 44

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

chloroform-d1

Location

supporting information

McKeever, Caitriona; Kaiser, Marcel; Rozas, Isabel; Journal of Medicinal Chemistry; vol. 56; nb. 3; (2013); p. 700 - 711, View in Reaxys

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4 of 44

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

tetrahydrofuran-d8

Temperature (NMR Spectroscopy) [°C]

0

Frequency (NMR Spectro- 500 scopy) [MHz] Location

supporting information

Choquette, Kimberly A.; Sadasivam, Dhandapani V.; Flowers, Robert A.; Journal of the American Chemical Society; vol.

132; nb. 49; (2010); p. 17396 - 17398, View in Reaxys 5 of 44

Description (NMR Spectroscopy)

Chemical shifts; Spectrum

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

tetrahydrofuran-d8

Temperature (NMR Spectroscopy) [°C]

0

Location

supporting information

Choquette, Kimberly A.; Sadasivam, Dhandapani V.; Flowers, Robert A.; Journal of the American Chemical Society; vol.

132; nb. 49; (2010); p. 17396 - 17398, View in Reaxys 6 of 44

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 7 of 44

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 8 of 44

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

various solvent(s)

Temperature (NMR Spectroscopy) [°C]

24.85

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Frequency (NMR Spectro- 500.13 scopy) [MHz] Giernoth, Ralf; Bankmann, Dennis; European Journal of Organic Chemistry; nb. 21; (2005); p. 4529 - 4532, View in Reaxys 9 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Bodor, Nicholas; Huang, Ming-Ju; Szantay Jr., Csaba; Szantay, Csaba; Tetrahedron; vol. 48; nb. 28; (1992); p. 5823 - 5830, View in Reaxys; Leardini, Rino; McNab, Hamish; Minozzi, Matteo; Nanni, Daniele; Reed, David; Wright, Andrew G.; Journal of the Chemical Society. Perkin Transactions 1; nb. 20; (2001); p. 2704 - 2710, View in Reaxys 10 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Burgess,H.; Donnelly,J.A.; Tetrahedron; vol. 47; (1991); p. 111, View in Reaxys; Karsch, Hans H.; Phosphorus and Sulfur and the Related Elements; vol. 12; (1981); p. 217 - 226, View in Reaxys; Thuong, Nguyen Thanh; Barbier, Christine; Asseline, Ulysse; Phosphorus and Sulfur and the Related Elements; vol. 14; (1983); p. 357 - 366, View in Reaxys; Azzouz, Abdelkrim; Didi, Mohamed-Amine; Revue Roumaine de Chimie; vol. 43; nb. 4; (1998); p. 309 - 313, View in Reaxys; Leardini, Rino; McNab, Hamish; Minozzi, Matteo; Nanni, Daniele; Reed, David; Wright, Andrew G.; Journal of the Chemical Society. Perkin Transactions 1; nb. 20; (2001); p. 2704 - 2710, View in Reaxys 11 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

acetone-d6

Satoh, Masahiro; Hirota, Minoru; Bulletin of the Chemical Society of Japan; vol. 69; nb. 9; (1996); p. 2619 - 2624, View in Reaxys 12 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

acetone-d6

Comment (NMR Spectroscopy)

1H-1H

Satoh, Masahiro; Hirota, Minoru; Bulletin of the Chemical Society of Japan; vol. 69; nb. 9; (1996); p. 2619 - 2624, View in Reaxys 13 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Sheppard; Turner; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 252; (1959); p. 506,513, View in Reaxys; Dailey; Shoolery; Journal of the American Chemical Society; vol. 77; (1955); p.

3977,3980, View in Reaxys; Shoolery; Journal of Chemical Physics; vol. 21; (1953); p. 1899, View in Reaxys; Allred; Rochow; Journal of the American Chemical Society; vol. 79; (1957); p. 5361,5362, View in Reaxys; Anderson; Physical Review; vol. <2>102; (1956); p. 151,159, View in Reaxys; Crawford; Foster; Canad.J.Physics; vol. 34; (1936); p. 653,657, View in Reaxys; Bothner-By; Naar-Colin; Journal of the American Chemical Society; vol. 80; (1958); p. 1728,1730; Annals of the New York Academy of Sciences; vol. 70; (1957); p. 833,836, View in Reaxys; Maslennikov, I. G.; Matus, L. I.; Kirichenko, L. N.; Lavrent'ev, A. N.; J. Gen. Chem. USSR (Engl. Transl.); vol. 61; nb. 2; (1991); p. 513,467, View in Reaxys; Friedrich, Edwin C.; Abma, Charles B.; Journal of the American Chemical Society; vol. 102; nb. 4; (1980); p. 1367 - 1371, View in Reaxys 14 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

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Solvents (NMR Spectroscopy)

CDCl3

Comment (NMR Spectroscopy)

1H-1H

Burgess,H.; Donnelly,J.A.; Tetrahedron; vol. 47; (1991); p. 111, View in Reaxys; Karsch, Hans H.; Phosphorus and Sulfur and the Related Elements; vol. 12; (1981); p. 217 - 226, View in Reaxys 15 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

25

Altona, Cornelis; Ippel, Johannes H.; Hoekzema, Aldert J. A. Westra; Erkelens, Cornelis; Groesbeek, Michel; Donders, Lambertus A.; Magnetic Resonance in Chemistry; vol. 27; nb. 6; (1989); p. 564 - 576, View in Reaxys 16 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

25

Comment (NMR Spectroscopy)

1H-1H.

Altona, Cornelis; Ippel, Johannes H.; Hoekzema, Aldert J. A. Westra; Erkelens, Cornelis; Groesbeek, Michel; Donders, Lambertus A.; Magnetic Resonance in Chemistry; vol. 27; nb. 6; (1989); p. 564 - 576, View in Reaxys 17 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

acetone-d6

Comment (NMR Spectroscopy)

13C-13C.

Krivdin, L. B.; Shcherbakov, V. V.; Glukhikh, N. G.; Kalabin, G. A.; Journal of Organic Chemistry USSR (English Translation); vol. 24; nb. 11; (1988); p. 2052 - 2056; Zhurnal Organicheskoi Khimii; vol. 24; nb. 11; (1988); p. 2276 - 2280, View in Reaxys 18 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CCl4

Kisilenko, A. A.; Baklan, V. F.; Khil'chevskii, A. N.; Kukhar', V. P.; J. Gen. Chem. USSR (Engl. Transl.); vol. 57; nb. 12; (1987); p. 2659 - 2662,2370 - 2372, View in Reaxys 19 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

26.9

Colucci, William J.; Jungk, Steven J.; Gandour, Richard D.; Magnetic Resonance in Chemistry; vol. 23; nb. 5; (1985); p. 335 - 343, View in Reaxys

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20 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

26.9

Comment (NMR Spectroscopy)

1H-1H.

Colucci, William J.; Jungk, Steven J.; Gandour, Richard D.; Magnetic Resonance in Chemistry; vol. 23; nb. 5; (1985); p. 335 - 343, View in Reaxys 21 of 44

Description (NMR Spectroscopy)

Spectrum

Nucleus (NMR Spectroscopy)

1H

Gutowsky; Pake; Journal of Chemical Physics; vol. 18; (1950); p. 162,169, View in Reaxys; Bain, Alex D.; Bornais, Jacques; Brownstein, Sydney; Canadian Journal of Chemistry; vol. 59; (1981); p. 723 - 730, View in Reaxys 22 of 44

Description (NMR Spectroscopy)

2D-NMR

Bain, Alex D.; Bornais, Jacques; Brownstein, Sydney; Canadian Journal of Chemistry; vol. 59; (1981); p. 723 - 730, View in Reaxys 23 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

30

Wiberg,K.B.; Patt,W.E.; Bailey,W.F.; Journal of Organic Chemistry; vol. 45; (1980); p. 4936, View in Reaxys 24 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectroscopy)

CDCl3

Temperature (NMR Spectroscopy) [°C]

45

Ejchart, Andrzej; Organic Magnetic Resonance; vol. 13; nb. 5; (1980); p. 368 - 371, View in Reaxys 25 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

Solvents (NMR Spectroscopy)

neat (no solvent)

Comment (NMR Spectroscopy)

1H-13C.

Spoormaker, Tom; Bie, Marius J. A. de; Recueil: Journal of the Royal Netherlands Chemical Society; vol. 99; nb. 6; (1980); p.

194 - 197, View in Reaxys 26 of 44

Description (NMR Spectroscopy)

NMR

Schnekenburger; Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft; vol. 303; (1970); p.

116,118-121, View in Reaxys; Bartuska; Maciel; Journal of Magnetic Resonance (1969-1992); vol. 5; (1971); p. 211, View in Reaxys; Vladimiroff; Malinowski; Journal of Chemical Physics; vol. 46; (1967); p. 1830,1837, View in Reaxys; Cavanaugh; Dailey; Journal of Chemical Physics; vol. 34; (1961); p. 1099,1100, View in Reaxys; Malinowski; Journal of the American Chemical Society; vol. 83; (1961); p. 4479,4480, View in Reaxys; Miyazima et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 1370, View in Reaxys; Heel; Zeil; Zeitschrift fuer Elektrochemie; vol. 64; (1960); p. 962,963-971; Chem.Abstr.; vol.

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55; nb. 115; (1961), View in Reaxys; Emsley; Tabony; Journal of Magnetic Resonance (1969-1992); vol. 17; (1975); p.

233,235, View in Reaxys; Mc Clellan; Nicksic; Journal of Physical Chemistry; vol. 69; (1965); p. 446, View in Reaxys; Chertkov; Sergeev; Theoretical and Experimental Chemistry; vol. 10; (1974); p. 692; ; p. 837, View in Reaxys; Jensen; Schaumburg; Acta Chemica Scandinavica (1947-1973); vol. 25; (1971); p. 663,665, View in Reaxys; Stahl-Lariviere; Organic Magnetic Resonance; vol. 6; (1974); p. 170,174, View in Reaxys; Stepanyants et al.; J. Anal. Chem. USSR (Engl. Transl.); vol. 31; (1976); p. 1770,1333,1334, View in Reaxys; Breitmaier et al.; Tetrahedron; vol. 29; (1973); p. 2485,2486,2488, View in Reaxys; Inamoto; Masuda; Tetrahedron Letters; (1977); p. 3287, View in Reaxys; Miyajima et al.; Chemical and Pharmaceutical Bulletin; vol. 18; (1970); p. 1489,1490, View in Reaxys; Maciel et al.; Journal of Physical Chemistry; vol. 76; (1972); p. 1466, View in Reaxys; Spoormaker; de Brie; Recueil des Travaux Chimiques des Pays-Bas; vol. 97; (1978); p.

135,136,137,140, View in Reaxys; Spiesecke; Schneider; Journal of Chemical Physics; vol. 35; (1961); p. 731,732,733, View in Reaxys; Miyajima; Takahashi; Journal of Physical Chemistry; vol. 75; (1971); p. 3766, View in Reaxys; Engelhardt et al.; Journal fuer Praktische Chemie (Leipzig); vol. 312; (1970); p. 935,942, View in Reaxys; Sempere; Regnier; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 276; (1973); p. 1587, View in Reaxys 27 of 44

Description (NMR Spectroscopy)

Spin-lattice relaxation time (T1)

Sempere et al.; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 74; (1977); p. 915, View in Reaxys 28 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C-Shift-Temperaturgradient

Schneider,H.J.; Freitag,W.; Journal of the American Chemical Society; vol. 98; (1976); p. 478, View in Reaxys 29 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C-chemische

Verschiebungen 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 30 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C-Kontakt-Shift mit Di-tert.-Butylnitroxid

Morishima et al.; Chemical Physics Letters; vol. 14; (1972); p. 372, View in Reaxys 31 of 44

Description (NMR Spectroscopy)

Spectrum

Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 17; (1969); p. 2049,2050, View in Reaxys; Martin; Martin; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 1048, View in Reaxys; Heel; Zeil; Zeitschrift fuer Elektrochemie; vol. 64; (1960); p. 962,963-971; Chem.Abstr.; vol. 55; nb. 115; (1961), View in Reaxys; Elleman et al.; Journal of Molecular Spectroscopy; vol. 7; (1961); p. 322,335, View in Reaxys 32 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

Protonendichte

Lazzeretti; Taddei; Tetrahedron Letters; (1969); p. 3025, View in Reaxys 33 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

chem. Verschieb. u. Elektronegativitaet

Bucci; Pietro; Journal of the American Chemical Society; vol. 90; (1968); p. 252, View in Reaxys 34 of 44

Description (NMR Spectroscopy)

Chemical shifts

Ebersole et al.; Journal of Physical Chemistry; vol. 68; (1964); p. 3430, View in Reaxys; Reddy; Goldstein; Journal of Chemical Physics; vol. 38; (1963); p. 2736,2737, View in Reaxys; Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 2120, View in Reaxys 35 of 44

Description (NMR Spectroscopy)

Chemical shifts

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Comment (NMR Spectroscopy)

d. Methylgruppen-Protonen i. CCl4, Trifluoressigsaeure, Trifluoressigsaeure-H2SO4 (Lsgm.-Effekte)

Peterson; Journal of Organic Chemistry; vol. 31; (1966); p. 439, View in Reaxys 36 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

d. Protonen am dek. C-Atom i. CCl4, Trifluoressigsaeure, Trifluoressigsaeure-H2SO4 (Lsgm.-Effekte)

Peterson; Journal of Organic Chemistry; vol. 31; (1966); p. 439, View in Reaxys 37 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

Lemieux et al.; Canadian Journal of Chemistry; vol. 40; (1962); p. 1955,1956, View in Reaxys; Juan; Gutowsky; Journal of Chemical Physics; vol. 37; (1962); p. 2198,2201, View in Reaxys; Malinowski; Journal of the American Chemical Society; vol.

83; (1961); p. 4479,4480, View in Reaxys; Ebersole et al.; Journal of Physical Chemistry; vol. 68; (1964); p. 3430, View in Reaxys; Reddy; Goldstein; Journal of Chemical Physics; vol. 38; (1963); p. 2736,2737, View in Reaxys 38 of 44

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

der gasfoermigen Substanz

Jouve et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 1079, View in Reaxys 39 of 44

Description (NMR Spectroscopy)

Spectrum

Comment (NMR Spectroscopy)

in CCl4

Jouve et al.; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 1079, View in Reaxys 40 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

in Cyclohexan,Dioxan,CCl4,Aceton,Nitromethan

Lumbroso et al.; Journal of Physical Chemistry; vol. 67; (1963); p. 2469,2471, View in Reaxys 41 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

13C

relativ zu Benzol

Schaefer et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 2969,2971, View in Reaxys 42 of 44

Description (NMR Spectroscopy)

Chemical shifts

Comment (NMR Spectroscopy)

1H

relativ zu Methan

Schaefer et al.; Canadian Journal of Chemistry; vol. 41; (1963); p. 2969,2971, View in Reaxys 43 of 44

Description (NMR Spectroscopy)

Spin-spin coupling constants

Comment (NMR Spectroscopy)

nucleus1-nucleus2:1H-1H.

Sheppard; Turner; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 252; (1959); p. 506,513, View in Reaxys; Glick; Bothner-By; Journal of Chemical Physics; vol. 25; (1956); p. 362, View in Reaxys; Anderson; Physical Review; vol. <2>102; (1956); p. 151,159, View in Reaxys 44 of 44

Description (NMR Spectroscopy)

Chemical shifts

Nucleus (NMR Spectroscopy)

13C

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Lauterbur; Annals of the New York Academy of Sciences; vol. 70; (1957); p. 841,844; Journal of Chemical Physics; vol. 26; (1957); p. 217, View in Reaxys IR Spectroscopy (29) 1 of 29

Description (IR Spectroscopy)

Bands

Melendez-Andreu; Annales de Chimie (Cachan, France); vol. 7; nb. 13; (1962); p. 695,702, View in Reaxys; Gotoh; Takenaka; Nippon Kagaku Zasshi; vol. 81; (1960); p. 1504,1505; Chem.Abstr.; nb. 3136; (1961), View in Reaxys; Teng, Chong; Wu, Hua; Zhang, Jian; Yang, Yan; Jia, Tianqing; Zhang, Shian; Sun, Zhenrong; RSC Advances; vol. 5; nb. 46; (2015); p. 37078 - 37084, View in Reaxys 2 of 29

Description (IR Spectroscopy)

Bands

Location

supporting information

Comment (IR Spectroscopy)

film

McKeever, Caitriona; Kaiser, Marcel; Rozas, Isabel; Journal of Medicinal Chemistry; vol. 56; nb. 3; (2013); p. 700 - 711, View in Reaxys 3 of 29

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

1460.0 1/cm

Azzouz, Abdelkrim; Didi, Mohamed-Amine; Revue Roumaine de Chimie; vol. 43; nb. 4; (1998); p. 309 - 313, View in Reaxys 4 of 29

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

gaseous matrix

Comment (IR Spectroscopy)

1480 - 1200 cm**(-1)

Hurst, Scott M.; Wilcox, C. F.; Bauer, S. H.; Journal of Chemical Physics; vol. 103; nb. 14; (1995); p. 5904 - 5910, View in Reaxys 5 of 29

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

3024 - 247 cm**(-1)

Hurst, Scott M.; Wilcox, C. F.; Bauer, S. H.; Journal of Chemical Physics; vol. 103; nb. 14; (1995); p. 5904 - 5910, View in Reaxys 6 of 29

Description (IR Spectroscopy)

Intensity of IR bands

Vincent-Geisse; deLara-Bentaquen; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 260; (1965); p. 6319, View in Reaxys; Kindness, A.; McKean, D. C.; Stewart, D.; Journal of Molecular Structure; vol. 224; (1990); p. 363 - 384, View in Reaxys 7 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

gas

Comment (IR Spectroscopy)

3100 - 2650 cm**(-1)

Kindness, A.; McKean, D. C.; Stewart, D.; Journal of Molecular Structure; vol. 224; (1990); p. 363 - 384, View in Reaxys 8 of 29

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

3020 - 294 cm**(-1)

Jung, Kyung-Hoon; Kang, Sung Hoon; Ro, Chul Un; Tschuikow-Roux, E.; Journal of Physical Chemistry; vol. 91; nb. 9; (1987); p. 2354 - 2358, View in Reaxys

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9 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

9000 - 7900 cm**(-1)

Salzer, Reiner; Weise, Dirk; Boenisch, Ulrike; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 25; nb. 7; (1985); p. 263 264, View in Reaxys 10 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

11400 - 10400 cm**(-1)

Salzer, Reiner; Weise, Dirk; Boenisch, Ulrike; Zeitschrift fuer Chemie (Stuttgart, Germany); vol. 25; nb. 7; (1985); p. 263 264, View in Reaxys 11 of 29

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

KBr

Comment (IR Spectroscopy)

1240 cm**(-1)

Trifonov, A. Z.; Nikolova, B. M.; Kuzmanova, R. B.; Ivanov, C.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 264; nb. 4; (1983); p. 664 - 672, View in Reaxys 12 of 29

Description (IR Spectroscopy)

Fine structure of IR bands

Ferner, S.; Salzer, R.; Borsdorf, R.; Zeitschrift fuer Physikalische Chemie (Leipzig); vol. 264; nb. 1; (1983); p. 178 - 180, View in Reaxys 13 of 29

Description (IR Spectroscopy)

IR

Bentley,F.F. et al.; Spectrochimica Acta; vol. 20; (1964); p. 105 - 126, View in Reaxys; Geiseler et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1007,1008, View in Reaxys; Perkampus; Baumgarten; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 496, View in Reaxys; Martin; Martin; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 257; (1963); p. 1048, View in Reaxys; Winther; Hummel; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 425,431, View in Reaxys; Dellepiane; Piseri; Gazzetta Chimica Italiana; vol. 106; (1976); p. 577,580, View in Reaxys; Fujiyama; Bulletin of the Chemical Society of Japan; vol. 44; (1971); p. 1194,1196, View in Reaxys; Hamada; Morishita; Spectroscopy Letters; vol. 13; (1980); p. 373,375, View in Reaxys; McKean et al; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 33; (1977); p. 865,866, View in Reaxys 14 of 29

Description (IR Spectroscopy)

Spectrum

Kinsella,E.; Coward,J.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 2139 2143, View in Reaxys; McDevitt et al.; Journal of Chemical Physics; vol. 42; (1965); p. 1173,1176, View in Reaxys; Gaufres; Bejaud-Bianchi; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 2249, View in Reaxys; Pardoe; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 203, View in Reaxys; Durig et al.; Journal of Chemical Physics; vol. 54; (1971); p. 460,462, 466, View in Reaxys; Kinumaki; Kozuka; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 3933, View in Reaxys 15 of 29

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

12500 - 5556 cm**(-1)

Le Fevre et al.; Australian Journal of Chemistry; vol. 12; (1959); p. 743, View in Reaxys; Tschulanowskii et al.; Izvestiya Akademii Nauk SSSR, Seriya Fizicheskaya; vol. 12; (1948); p. 628,633; Chem.Abstr.; (1950); p. 4332, View in Reaxys 16 of 29

Description (IR Spectroscopy)

Fine structure of IR bands

Comment (IR Spectroscopy)

bei 769.9 cm-1.

Dixon; Spectrochimica Acta; vol. 9; (1957); p. 59,60, View in Reaxys 17 of 29

Description (IR Spectroscopy)

Spectrum

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Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

1493 - 699 cm**(-1); fest.

Brown; Sheppard; Transactions of the Faraday Society; vol. 50; (1954); p. 535,536, View in Reaxys 18 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1493 - 500 cm**(-1); Fluessigkeit.

Brown; Sheppard; Transactions of the Faraday Society; vol. 50; (1954); p. 535,536, View in Reaxys 19 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

714 - 526 cm**(-1); in fluessigem Aethylbromid.

Mortimer; Blodgett; Daniels; Journal of the American Chemical Society; vol. 69; (1947); p. 823, View in Reaxys 20 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

9434 - 6250 cm**(-1); in fluessigem Aethylbromid bei 20grad.

Suhrmann; Klein; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 50; (1941); p. 50, View in Reaxys 21 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

6667 - 667 cm**(-1); in fluessigem Aethylbromid.

Cross; Daniels; Journal of Chemical Physics; vol. 1; (1933); p. 49,50, View in Reaxys; Plum; Journal of Chemical Physics; vol.

5; (1937); p. 174, View in Reaxys 22 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

16667 - 10309 cm**(-1); in fluessigem Aethylbromid bei 25grad.

Barchewitz; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 203; (1936); p. 1246; Annales de Physique (Paris, France); vol. <11>11; (1939); p. 309,310,311,312, View in Reaxys 23 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

14286 - 10526 cm**(-1); in fluessigem Aethylbromid bei 12grad und 36grad.

Ganz; Annalen der Physik (Weinheim, Germany); vol. <5> 26; (1936); p. 331,341, 343, View in Reaxys 24 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

12500 - 4545 cm**(-1); in fluessigem Aethylbromid.

Trabert; Schaum; Z.wiss.Phot.; vol. 35; p. 159,162,167; Chem. Zentralbl.; vol. 107; nb. II; (1936); p. 2122, View in Reaxys 25 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

11364 - 10753 cm**(-1); in fluessigem Aethylbromid bei 25grad.

Timm; Mecke; Zeitschrift fuer Physik; vol. 98; (1936); p. 369, View in Reaxys; Vierling; Mecke; Zeitschrift fuer Physik; vol.

99; (1936); p. 207,211, View in Reaxys 26 of 29

Description (IR Spectroscopy)

Spectrum

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Comment (IR Spectroscopy)

6667 - 667 cm**(-1); von Dampf bei 25grad unter vermindertem Druck.

Cross; Daniels; Journal of Chemical Physics; vol. 1; (1933); p. 49,50, View in Reaxys 27 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

8929 - 5128 cm**(-1); in fluessigem Aethylbromid.

Spence; Easley; Physical Review; vol. <2>34; (1929); p. 733,734,737, View in Reaxys 28 of 29

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Bonino; Gazzetta Chimica Italiana; vol. 55; (1925); p. 342, View in Reaxys; Ellis; Physical Review; vol. <2> 23; (1924); p. 54; Journal of the American Chemical Society; vol. 51; (1929); p. 1387; Chem. Zentralbl.; vol. 95; nb. I; (1924); p. 1635, View in Reaxys 29 of 29

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

4000 - 400 cm**(-1); Dampf.

Bak et al; Acta Chemica Scandinavica (1947-1973); <1958>2021,2023, View in Reaxys Mass Spectrometry (11) Description (Mass Location Spectrometry) high resolution mass spectrometry (HRMS); electrospray ionisation (ESI); spectrum

Comment (Mass Spectrometry)

Paragraph 0194

References Patent; BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM; MARTIN, Stephen, F.; SAHN, James, J.; LINKENS, Kathryn, Taylor; (119 pag.); WO2017/190109; (2017); (A1) English, View in Reaxys

time-of-flight mass spectra (TOFMS); spectrum

Teng, Chong; Wu, Hua; Zhang, Jian; Yang, Yan; Jia, Tianqing; Zhang, Shian; Sun, Zhenrong; RSC Advances; vol. 5; nb. 46; (2015); p. 37078 37084, View in Reaxys

high resolution mass spectrometry (HRMS); electron impact (EI); spectrum

supporting information

McKeever, Caitriona; Kaiser, Marcel; Rozas, Isabel; Journal of Medicinal Chemistry; vol. 56; nb. 3; (2013); p. 700 - 711, View in Reaxys

GCMS (Gas chromatography mass spectrometry); Spectrum

supporting information

Yang, Guoqiang; Shen, Chaoren; Zhang, Liang; Zhang, Wanbin; Tetrahedron Letters; vol. 52; nb. 39; (2011); p. 5032 - 5035, View in Reaxys

spectrum; time-offlight mass spectra (TOFMS)

Xu, Dadong; Price, Roosevelt J.; Huang, Jianhua; Jackson, William M.; Zeitschrift fur Physikalische Chemie; vol. 215; nb. 2; (2001); p. 253 - 271, View in Reaxys

chemical ionization (CI)

collisional activation

Harrison, Alex. G.; Organic Mass Spectrometry; vol. 22; (1987); p. 637 641, View in Reaxys

spectrum

field ionization

Sokolov, V. V.; Grishin, N. N.; Petrov, A. A.; Journal of Organic Chemistry USSR (English Translation); vol. 18; (1982); p. 1586 - 1591; Zhurnal Organicheskoi Khimii; vol. 18; nb. 9; (1982); p. 1813 - 1819, View in Reaxys

spectrum; electron impact (EI)

Hanner, A. W.; Abbey, L. E.; Bostwick, D. E.; Burgess, E. M.; Moran, T. F.; Organic Mass Spectrometry; vol. 17; nb. 1; (1982); p. 19 - 28, View in Reaxys Pottie; Hamill; Journal of Physical Chemistry; vol. 63; (1959); p. 877, 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; Olmsted et al.; Journal of Chemical Physics; vol.

40; (1964); p. 2114,2116, View in Reaxys; McLafferty; Analytical Chemistry; vol. 34; (1962); p. 2,8, View in Reaxys; Alberti et al.; International Journal of Mass Spectrometry and Ion Physics; vol. 14; (1974); p. 89,96,

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View in Reaxys; Bursey; Wolfe; Organic Mass Spectrometry; vol. 1; (1968); p. 543, View in Reaxys appearance potentials appearance potentials

Tsuda; Hamill; Journal of Chemical Physics; vol. 41; (1964); p. 2713,2714, View in Reaxys; Gruetzmacher; Organic Mass Spectrometry; vol. 3; (1970); p. 131,134, View in Reaxys positiver Ionen bei Elektronenstoss.

Irsa; Journal of Chemical Physics; vol. 26; (1957); p. 18,19, View in Reaxys

UV/VIS Spectroscopy (18) 1 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. buffer

Absorption Maxima (UV/ VIS) [nm]

479

Li, Yong; Yang, Zheng-Yin; Journal of Fluorescence; vol. 20; nb. 1; (2010); p. 329 - 342, View in Reaxys 2 of 18

Description (UV/VIS Spectroscopy)

Vacuum-UV spectrum

Comment (UV/VIS Spectroscopy)

gas

Giuliani; Motte-Tollet; Delwiche; Mason; Jones; Gingell; Walker; Hubin-Franskin; Journal of Chemical Physics; vol. 112; nb. 14; (2000); p. 6285 - 6292, View in Reaxys 3 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gas

Giuliani; Motte-Tollet; Delwiche; Mason; Jones; Gingell; Walker; Hubin-Franskin; Journal of Chemical Physics; vol. 112; nb. 14; (2000); p. 6285 - 6292, View in Reaxys 4 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

cyclohexane

Comment (UV/VIS Spectroscopy)

25000 - 52500 1/cm

Zheng, Xuming; Phillips, David Lee; Journal of Chemical Physics; vol. 110; nb. 3; (1999); p. 1638 - 1649, View in Reaxys 5 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

200 - 260 nm

Zhang; Yang; Wang; Fuss; Weizbauer; Journal of Fluorine Chemistry; vol. 88; nb. 2; (1998); p. 153 - 168, View in Reaxys 6 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

gaseous matrix

Comment (UV/VIS Spectroscopy)

160 - 210 nm

Penner, Abraham; Amirav, Aviv; Journal of Chemical Physics; vol. 93; nb. 12; (1990); p. 8576 - 8579, View in Reaxys 7 of 18

Description (UV/VIS Spectroscopy)

Vacuum-UV spectrum

Penner, Abraham; Amirav, Aviv; Journal of Chemical Physics; vol. 93; nb. 12; (1990); p. 8576 - 8579, View in Reaxys 8 of 18

Description (UV/VIS Spectroscopy)

Spectrum

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Comment (UV/VIS Spectroscopy)

181.82 - 129.87 nm

Felps, W. S.; Scott, J. D.; Findley, G. L.; McGlynn, S. P.; Journal of Chemical Physics; vol. 74; nb. 9; (1981); p. 4832 - 4838, View in Reaxys 9 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Spring; Recueil des Travaux Chimiques des Pays-Bas; vol. 16; (1897); p. 1, View in Reaxys; Baker; Russell; Journal of Molecular Spectroscopy; vol. 69; (1978); p. 211,214-215, 218, View in Reaxys 10 of 18

Description (UV/VIS Spectroscopy)

UV/VIS

Nelson; Applied Spectroscopy; vol. 23; (1969); p. 133,134, View in Reaxys 11 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

155 - 280 nm

Astoin et al.; Journal de Physique et le Radium; vol. <8>19; (1958); p. 507, View in Reaxys 12 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

AlBr3

Korschak; Lebedew; Zhurnal Obshchei Khimii; vol. 18; (1948); p. 1768; Chem.Abstr.; (1949); p. 2930, View in Reaxys 13 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

von fluessigem Aethylbromid.

Korschak; Lebedew; Zhurnal Obshchei Khimii; vol. 18; (1948); p. 1768; Chem.Abstr.; (1949); p. 2930, View in Reaxys 14 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

von gasfoermigem Aethylbromid bei 1-369 mm Druck und 19grad.

Hukumoto; Sci. Rep. Tohoku Univ., Ser. 1: Phys., Chem., Astron.; vol. <1>21; (1932); p. 165,916,924; Chem. Zentralbl.; vol.

104; nb. I; (1933); p. 3681, View in Reaxys; Price; Journal of Chemical Physics; vol. 3; (1935); p. 365, View in Reaxys; Porret; Goodeve; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 165; (1938); p. 38,39, View in Reaxys; Hukumoto; Journal of Chemical Physics; vol. 3; (1935); p. 165; Sci. Rep. Tohoku Univ., Ser. 1: Phys., Chem., Astron.; vol. <1> 23; (1934); p. 846; Chem. Zentralbl.; vol. 107; nb. I; (1936); p. 4534, View in Reaxys 15 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

von gasfoermigem und fluessigem Aethylbromid.

Hukumoto; Sci. Rep. Tohoku Univ., Ser. 1: Phys., Chem., Astron.; vol. <1>22; (1933); p. 164,21,23,26; Chem. Zentralbl.; vol.

104; nb. II; (1933); p. 1968, View in Reaxys 16 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

von gasfoermigem Aethylbromid bei 7-405 mm Druck und 15grad bzw. 35grad.

Iredale; Mills; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol.

133; (1931); p. 433,435, View in Reaxys 17 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Lederle; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 10; (1930); p. 131, View in Reaxys

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18 of 18

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

reiner Substanz.

Hantzsch; Chemische Berichte; vol. 58; (1925); p. 632, View in Reaxys ESR Spectroscopy (2) 1 of 2

Description (ESR Spectro- ESR scopy) Neta et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 1654,1661, View in Reaxys; Stepanov et al.; International Journal of Chemical Kinetics; vol. 10; (1978); p. 637,638-639, 647, View in Reaxys; Maguire; Bernheim; Journal of Magnetic Resonance (1969-1992); vol. 4; (1971); p. 167, View in Reaxys

2 of 2

Description (ESR Spectro- Spectrum scopy) Ayscough; Thomson; Transactions of the Faraday Society; vol. 58; (1962); p. 1477,1483, View in Reaxys; Mitchell et al.; Journal of Chemical Physics; vol. 36; (1962); p. 1095, View in Reaxys; Egland et al.; Journal of Physical Chemistry; vol. 75; (1971); p. 467, View in Reaxys

NQR Spectroscopy (3) Description (NQR Nucleus (NQR Spectroscopy) Spectroscopy)

References

Nuclear quadrupole resonance

Hooper; Bray; Journal of Chemical Physics; vol. 33; (1960); p. 334,336, View in Reaxys; Feshin, V. P.; Voronkov, M. G.; Romanenko, L. S.; Ignat'eva, L. P.; Dolgushin, G. V.; J. Gen. Chem.

USSR (Engl. Transl.); vol. 54; nb. 6; (1984); p. 1312 - 1314,1175 - 1177, View in Reaxys; Semin; Petukhov; Bryukhova; Boguslavskii; Russian Chemical Bulletin; vol. 47; nb. 6; (1998); p. 1118 - 1121, View in Reaxys

Nuclear quadrupole 79Br coupling constants

Zeldes; Livingston; Journal of Chemical Physics; vol. 21; (1953); p. 1418, View in Reaxys; Kojima et al.; Journal of Chemical Physics; vol. 21; (1953); p. 1415, View in Reaxys; Wagner; Dailey; Journal of Chemical Physics; vol. 26; (1957); p. 1588,1589,1591, View in Reaxys

Nuclear quadrupole 81Br coupling constants

Zeldes; Livingston; Journal of Chemical Physics; vol. 21; (1953); p. 1418, View in Reaxys; Kojima et al.; Journal of Chemical Physics; vol. 21; (1953); p. 1415, View in Reaxys; Wagner; Dailey; Journal of Chemical Physics; vol. 26; (1957); p. 1588,1589,1591, View in Reaxys

Rotational Spectroscopy (1) Description (Rota- Comment (Rotational Spectroscotional Spectroscopy) py) Microwave spectrum

References

bei 22000 NMz und Wagner; Dailey; Journal of Chemical Physics; vol. 26; (1957); p. 1588,1589,1591, 29000 MHz. View in Reaxys; Lide; Journal of Chemical Physics; vol. 30; (1959); p. 37, View in Reaxys

Raman Spectroscopy (9) Description (Ram- Comment (Raman an Spectroscopy) Spectroscopy)

References

Raman

Hamada; Morishita; Spectroscopy Letters; vol. 13; (1980); p. 373,375, View in Reaxys; Durig et al.; Journal of Chemical Physics; vol. 60; (1974); p. 1754, View in Reaxys; Bartoli; Litovitz; Journal of Chemical Physics; vol. 56; (1972); p. 404,407, View in Reaxys

Raman intensities

Nestor; Lippincott; Journal of Raman Spectroscopy; vol. 1; (1973); p. 305, View in Reaxys

Spectrum

Gaufres; Bejaud-Bianchi; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 27; (1971); p. 2249, View in Reaxys; Hornischer; Moser; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 73; (1970); p. 118,126, View in Reaxys

Bands

Murphy et al.; Applied Spectroscopy; vol. 23; (1969); p. 211,215, View in Reaxys

Spectrum

von fluessigem Aethylbromid

Wagner; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 40; (1938); p. 442,445,449; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 45; (1940); p. 81, View in Reaxys; Dadieu; Kohlrausch; Monatshefte fuer Chemie; vol. 55; (1930); p. 70,77,; Monatshefte fuer Chemie; vol. 57; (1931); p. 489, View in Reaxys; Cross; van Vleck; Journal of Chemical Physics; vol. 1; (1933); p. 350, View in Reaxys; Langseth; Bak; Danske Vid.Selsk.mat.-fys.Medd.; vol. 24; nb. 3; (1947); p. 8; Chem.Abstr.; (1948); p. 459, View in Reaxys; de Hemptinne; Velghe; Physica; vol. 5; (1938); p. 958; Chem. Zentralbl.; vol.

110; nb. I; (1939); p. 4590, View in Reaxys; Voge; Journal of Chemical Physics; vol. 2; (1934); p.

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264, View in Reaxys; Soederqvist; Zeitschrift fuer Physik; vol. 59; (1929); p. 449,459, View in Reaxys; Cleeton; Dufford; Physical Review; vol. <2> 37; (1931); p. 362,369, View in Reaxys; Bhagavantam; Venkateswaran; Proceedings of the Royal Society of London, Series A: Mathematical, Physical and Engineering Sciences; vol. 127; (1930); p. 360,370, View in Reaxys Bands

Valenzschwingung der C-Br-Bindung

Kohlrausch; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 18; (1932); p. 64, View in Reaxys; Bartholome; Teller; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 19; (1932); p. 385, View in Reaxys; Langseth; Bernstein; Bak; Journal of Chemical Physics; vol. 8; (1940); p. 430, View in Reaxys; Harkins; Bowers; Journal of the American Chemical Society; vol. 53; (1931); p. 2426, View in Reaxys; Mortimer; Blodgett; Daniels; Journal of the American Chemical Society; vol. 69; (1947); p. 823, View in Reaxys; Harkins; Haun; Journal of the American Chemical Society; vol. 54; (1932); p. 3923, View in Reaxys

Bands

Intensitaet der CBr-Linie in CCl4Loesung

Tatewski; Zhurnal Fizicheskoi Khimii; vol. 20; p. 129; Chem.Abstr.; (1946); p. 5644, View in Reaxys

Degree of depolarization of Raman bands

verschiedener Ram- Wagner; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, anfrequenzen.

Aufbau der Materie; vol. 45; (1940); p. 88,91, View in Reaxys

Degree of depolarization of Raman bands

bei der molekularen Lichtstreuung in fluessigem Aethylbromid.

Krishnan; Chem. Zentralbl.; vol. 97; nb. I; (1926); p. 838, View in Reaxys; Canals; Peyrot; Bulletin de la Societe Chimique de France; vol. <4>53; (1933); p. 744, View in Reaxys; Canals; Cauquil; Peyrot; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol.

198; (1934); p. 472, View in Reaxys

Luminescence Spectroscopy (2) Description (Lumi- References nescence Spectroscopy) Luminescence spectrum

Han, Ke-Li; Zhang, Li; Xu, Da-Li; He, Guo-Zhong; Lou, Nan-Quan; Journal of Physical Chemistry A; vol. 105; nb.

13; (2001); p. 2956 - 2960, View in Reaxys

Luminescence quenching

Kropp; Burton; Journal of Chemical Physics; vol. 37; (1962); p. 1742,1746, View in Reaxys; Hechner et al.; High Energy Chemistry; vol. 12; (1978); p. 285,286, View in Reaxys

Other Spectroscopic Methods (3) Description (Other Comment (Other Spectroscopic Spectroscopic Methods) Methods)

References

Photoelectron spec- vibrational analysis trum

Giuliani; Motte-Tollet; Delwiche; Mason; Jones; Gingell; Walker; Hubin-Franskin; Journal of Chemical Physics; vol. 112; nb. 14; (2000); p. 6285 - 6292, View in Reaxys

ESCA

Ascone, I.; D'Angelo, P.; Pavel, N. V.; Journal of Physical Chemistry; vol. 98; nb. 11; (1994); p.

2982 - 2990, View in Reaxys

Photoelectron spectrum

Brogli; Heilbronner; Helvetica Chimica Acta; vol. 54; (1971); p. 1423,1425, View in Reaxys; Kimura et al.; Bulletin of the Chemical Society of Japan; vol. 46; (1973); p. 373,374, View in Reaxys; Utsunomiya, Chikatoshi; Kobayashi, Tsunetoshi; Nagakura, Saburo; Bulletin of the Chemical Society of Japan; vol. 53; nb. 5; (1980); p. 1216 - 1220, View in Reaxys; Ohno, Koichi; Imai, Keitaro; Harada, Yoshiya; Journal of the American Chemical Society; vol.

107; nb. 26; (1985); p. 8078 - 8082, View in Reaxys

Transport and Distribution (1) 1 of 1

Type (Transport and Distribution)

release

Media (Transport and Distribution)

macroalgae-air

Results

release rate ranged from 0 to 400 ng g-1 wet alga weight d-1; formation mechanism discussed

Method, Remarks (Transport and Distribution)

Arctic and Antarctic macroalgae (Phaeophyta, Rhodophyta, Chlorophyta) placed in sealed glass vessel with nat. seawater; isol. and identif. by purge and trap technique; GC column with high stationary phase thickness

Laturnus; Chemosphere; vol. 31; nb. 6; (1995); p. 3387 - 3395, View in Reaxys Abiotic Degradation, Hydrolysis (1) 1 of 1

Type (Abiotic Degradation, Hydrolysis)

reduction

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Temperature (Abiotic Deg- 20 radation, Hydrolysis) [°C] Method, Remarks (Abiotic closed vapor:water batch system, metallic iron 8 g, 140 h, GC-ECD Degradation, Hydrolysis) Degradation Product (Abiotic Degradation, Hydrolysis)

ethene; ethane

Rajagopal, Venkat K.; Burris, David R.; Environmental Toxicology and Chemistry; vol. 18; nb. 8; (1999); p. 1779 - 1782, View in Reaxys Use (2) Use Pattern

References

Halogen promoting component for carbonylation catalyst

Patent; EASTMAN CHEMICAL COMPANY; EP1153007; (2007); (B1) English, View in Reaxys

Quaternization of Patent; Russell, Alan J.; Koepsel, Richard; Lee, Sang Boem; Matyjaszewski, Krzysztof; US2006/8490; (2006); polymerized mono- (A1) English, View in Reaxys mer in biocidal articles Medchem (34) 1 of 34

Substance Effect

Carcinogenic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : tumor incidenceTarget : B6C3F1 mouseBioassay : 50 male and 50 female; National Toxicology Program Rodent Bioassay (NTPRB); transgenic model system; animals received title comp. for 2 years; animals were examined for the presence of tumors in various tissues and organs; histopathology

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Route of Adm.

inhalational administration

Qualitative Results

summary level of evidence: equivocal evidence for males and clear evidence for females

Measurement Parameter

qualitative

Johnson; Environmental and Molecular Mutagenesis; vol. 34; nb. 4; (1999); p. 234 - 245, View in Reaxys 2 of 34

Substance Effect

Carcinogenic

Bioassay Category

In Vivo (Animal models)

Bioassay Name

In vivo Measurement

Bioassay Details

Effect : tumor incidenceTarget : F344 ratBioassay : 31 tissue/body sites tested in males: ur. blad., bone, brain, esophage, forestomach, intestine, kidney, liver, lung, mammary gland, nose/nasal and oral cavities, pancreatic acinar and islet cells, parathyroid, pituitary gland (pars distalis), and others 50 male and 50 female; National Toxicology Program Rodent Bioassay (NTPRB); transgenic model system; title comp. in food; after 2 years the animals were examined for the presence of tumors in various tissues and organs; histopathology

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Route of Adm.

inhalational administration

Qualitative Results

summary level of evidence: some evidence for males and clear evidence for females; male rats: increased incidence in brain and lung. adrenal pheochromocytoma was observed

Measurement Parameter

qualitative

Johnson; Environmental and Molecular Mutagenesis; vol. 34; nb. 4; (1999); p. 234 - 245, View in Reaxys 3 of 34

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

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Bioassay Details

Target : CHO-WBL cellsBioassay : positive control: mitomycin-C cells treated with title comp. for 24 h at 37 deg C; stained with acridine orange and analysed by epi-fluorescence microscopy; cytotoxicity determined by measuring relative nuclear division (RD%)

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Dose

5000 mg/L

Qualitative Results

RD=93.5% at high dose; table No effect

Measurement Parameter

qualitative

Sobol; Engel; Rubitski; Ku; Aubrecht; Schiestl; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 633; nb. 2; (2007); p. 80 - 94, View in Reaxys 4 of 34

Substance Effect

Cytotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Saccharomyces cerevisiae RS112Bioassay : cells treated with title comp. for 17 h at 30 deg C; plated onto complete medium to determine number of survivors (relative survival, RS%)

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Dose

3650 mg/L

Qualitative Results

title comp. dose-dependently decreased RS (to 0.4% at high dose); table

Measurement Parameter

qualitative

Sobol; Engel; Rubitski; Ku; Aubrecht; Schiestl; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 633; nb. 2; (2007); p. 80 - 94, View in Reaxys 5 of 34

Substance Effect

Genotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : CHO-WBL cellsBioassay : positive control: mitomycin-C clastogenicity assay; cells treated with title comp. for 24 h at 37 deg C; stained with acridine orange and analysed by epi-fluorescence microscopy for micronulei

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Dose

5000 mg/L

Measurement Parameter

qualitative

Qualitative value

NA

Measurement pX

1

Sobol; Engel; Rubitski; Ku; Aubrecht; Schiestl; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 633; nb. 2; (2007); p. 80 - 94, View in Reaxys 6 of 34

Substance Effect

Genotoxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Saccharomyces cerevisiae RS112Bioassay : deletion recombination assay; cells treated with title comp. for 17 h at 30 deg C; DNA deletions determined by scoring colonies growing on agar medium lacking histidine

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Dose

3650 mg/L

Qualitative Results

title comp. dose-dependently increased frequency of deletion recombination events (17.5-fold at high dose)

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Measurement Parameter

qualitative

Sobol; Engel; Rubitski; Ku; Aubrecht; Schiestl; Mutation Research - Genetic Toxicology and Environmental Mutagenesis; vol. 633; nb. 2; (2007); p. 80 - 94, View in Reaxys 7 of 34

8 of 34

9 of 34

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : dehalogenase activity |enzyme; examination of Bioassay : the unit of dehalogenase activity (U): amount of enzyme catalysing the release of 1 Îźmol Cl(-)/min/mg soluble protein; reference: dehalogenation rate of 1-chlorobutane resting cell systems; relative activity of resuspended whole cells induced by 1-chlorobutane (halidohydrolase-type dehalogenase) or hexadecane (oxygenasetype dehalogenase); 100 mM Tris-SO4 buffer pH 8.0; 50-100 mg wet wt cell/ml; 30 deg C; 200 rpm

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Dose

10 mM

Qualitative Results

relative activity: 92 for halidohydrolase-type activity (reference: 44 mU/mg protein as 100), 124 for oxygenase-type activity (reference: 3.67 mU/mg protein as 100)

Measurement Parameter

qualitative

Target Name

enzyme

Target Synonyms

enzyme

Target, Subunit, Species

enzyme

Target Mutant/Chimera Details

enzyme:Wild

Target Transfection

Non Transfected

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : |enzyme; examination of Bioassay : halide production determined spectrophotometrically at 460 nm using mercuric thiocyanate and ferric ammonium dehalogenation assay performed at 30 deg C for up to 45 min; activity of hydrolytic dehalogenation of the title comp. by enzyme relative to 1-chlorobutane assessed

Substance RN

1209224View in Reaxys

Substance Name

216583

Substance Dose

10 mM

Qualitative Results

enzyme showed 46 percent activity of hydrolytic dehalogenation of the title comp. (100 percent for 1-chlorobutane)

Measurement Parameter

qualitative

Substance Effect

Carcinogenic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Effect : carcinogenicityBioassay : animal

Substance RN

1209224View in Reaxys

Substance Name

216583

Qualitative Results

TD50 -0.136

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Measurement Parameter

qualitative

Toropov; Toropova; Benfenati; European Journal of Medicinal Chemistry; vol. 45; nb. 9; (2010); p. 3581 - 3587, View in Reaxys 10 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Substance RN

1209224View in Reaxys

Substance Name

216583

Qualitative Results

the mutagenic potency and the mutagenic dose for Salmonella typhimurium

Measurement Parameter

qualitative

Eriksson; Hellberg; Johansson; Jonsson; Sjoestroem; Wold; Berglind; Karlsson; Acta chemica Scandinavica (Copenhagen, Denmark : 1989); vol. 45; nb. 9; (1991); p. 935 - 944, View in Reaxys 11 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Bioassay : Arctic and Antarctic macroalgae (Phaeophyta, Rhodophyta, Chlorophyta) placed in sealed glass vessel with nat. seawater; isol. and identif. by purge and trap technique; GC column with high stationary phase thickness

Substance RN

1209224View in Reaxys

Substance Name

216583

Qualitative Results

release release rate ranged from 0 to 400 ng g-1 wet alga weight d-1; formation mechanism discussed

Measurement Parameter

qualitative

Laturnus; Chemosphere; vol. 31; nb. 6; (1995); p. 3387 - 3395, View in Reaxys 12 of 34

Substance Effect

Toxic

Bioassay Category

In Vitro (Efficacy)

Bioassay Name

In Vitro (others)

Bioassay Details

Target : Shk1 cellsBioassay : Shk1 is genetically modified luminescent bacterium whose original strain Pseudomonad, isolated from the activated sludge; control = buffer (pH: 7) continuous-stirred tank reactor; dilution rate of 0.52 h-1; pH 7; 22 deg C; bioluminescence measured after exposure for 5 min

Substance RN

1209224View in Reaxys

Substance Name

216583

Measurement Parameter

EC50

Unit

mg/L

Quantitative value

2186

Measurement pX

1.7

Ren, Shijin; Frymier, Paul D; Water Research; vol. 36; nb. 17; (2002); p. 4406 - 4414, View in Reaxys 13 of 34

Substance Action on Target

Inhibitor

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Log of reciprocal concentration of the compound required for inhibition of narcotic action on frog heart

Biological Species/NCBI ID

Anura

Substance RN

1209224View in Reaxys

Measurement Parameter

pIC50

Measurement Object

Narcotic action on frog heart

Quantitative value

1.48

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Measurement pX

1.48

Hansch; Anderson; Journal of medicinal chemistry; vol. 10; nb. 5; (1967); p. 745 - 753, View in Reaxys 14 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Difference between observed and calculated concentration value of compound required for inhibition of narcotic action on frog heart

Biological Species/NCBI ID

Anura

Organs/Tissues

heart

Substance RN

1209224View in Reaxys

Qualitative Results

Delta log (I/C) not calculated

Measurement Parameter

qualitative

Measurement Object

delta log (I/C)

Hansch; Anderson; Journal of medicinal chemistry; vol. 10; nb. 5; (1967); p. 745 - 753, View in Reaxys 15 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Concentration of the compound required for tadpole narcosis

Substance RN

1209224View in Reaxys

Measurement Parameter

pIC50

Measurement Object

Tadpole narcosis

Quantitative value

2.57

Measurement pX

2.57

Leo; Hansch; Church; Journal of medicinal chemistry; vol. 12; nb. 5; (1969); p. 766 - 771, View in Reaxys 16 of 34

Bioassay Category

Metabolism/Transport

Bioassay Details

Half life hydrolysis rate of the resultant mixed ester

Substance RN

1209224View in Reaxys

Measurement Parameter

t1/2 el

Unit

second

Qualitative value

=

Quantitative value

3.27

Steinberg; Lieske; Boldt; Goan; Podall; Journal of medicinal chemistry; vol. 13; nb. 3; (1970); p. 435 - 446, View in Reaxys 17 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Effective dose of the compound required to inhibit reflex in mouse was determined (gas or vapor under pressure carrying effect in half the individuals in the control group)

Biological Species/NCBI ID

mouse

Substance RN

1209224View in Reaxys

Measurement Parameter

Activity

Measurement Object

Lg 1/P Ed50

Quantitative value

1.4

Leszek Bober; Piotr Kawczak; Tomasz Baczek; Letters in drug design & discovery; vol. 9; nb. 6; (2012); p. 595 - 603, View in Reaxys 18 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Logarithm of effective anesthetic pressure (p) of the compound was determined in mice

Biological Species/NCBI ID

mouse

Substance RN

1209224View in Reaxys

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Qualitative Results

log 1/p not calculated

Measurement Parameter

qualitative

Measurement Object

log (1/p)

Hansch; Vittoria; Silipo; Jow; Journal of Medicinal Chemistry; vol. 18; nb. 6; (1975); p. 546 - 548, View in Reaxys 19 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Tadpole narcotic activity of the compound was determined

Substance RN

1209224View in Reaxys

Qualitative Results

log 1/Cnar not calculated

Measurement Parameter

qualitative

Measurement Object

log (1/Cnar)

Agrawal, Vijay K.; Chaturvedi, Sanjeev; Abraham, Michael H.; Khadikar, Padmakar V.; Bioorganic and Medicinal Chemistry; vol. 11; nb. 20; (2003); p. 4523 - 4533, View in Reaxys 20 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal concentration upon inhalation;Inhalation;1 hour

Biological Species/NCBI ID

rat

Substance RN

1209224View in Reaxys

Substance Route of Adm.

inhalational administration

Measurement Parameter

qualitative

Qualitative value

Not Published

Quantitative value

26980

Material Safety Data Sheet, View in Reaxys 21 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose upon Intraperitoneal administration;Intraperitoneal

Biological Species/NCBI ID

rat

Substance RN

1209224View in Reaxys

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

=

Quantitative value

1750

Material Safety Data Sheet, View in Reaxys 22 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose upon oral administration;Oral

Biological Species/NCBI ID

rat

Substance RN

1209224View in Reaxys

Substance Route of Adm.

oral administration

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

=

Quantitative value

1350

Material Safety Data Sheet, View in Reaxys

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23 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal dose upon Intraperitoneal administration;Intraperitoneal

Biological Species/NCBI ID

mouse

Substance RN

1209224View in Reaxys

Substance Route of Adm.

intraperitoneal administration

Measurement Parameter

LD50

Unit

mg/kg

Qualitative value

=

Quantitative value

2850

Material Safety Data Sheet, View in Reaxys 24 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lowest published toxic concentration;Inhalation;6 hour

Biological Species/NCBI ID

rat

Substance RN

1209224View in Reaxys

Substance Route of Adm.

inhalational administration

Measurement Parameter

qualitative

Qualitative value

Not Published

Material Safety Data Sheet, View in Reaxys 25 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lowest published toxic concentration;Inhalation;6 hour

Biological Species/NCBI ID

rat

Substance RN

1209224View in Reaxys

Substance Route of Adm.

inhalational administration

Measurement Parameter

qualitative

Qualitative value

Not Published

Quantitative value

1600

Material Safety Data Sheet, View in Reaxys 26 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lethal concentration upon inhalation;Inhalation;1 hour

Biological Species/NCBI ID

mouse

Substance RN

1209224View in Reaxys

Substance Route of Adm.

inhalational administration

Unit

ppm

Qualitative value

=

Quantitative value

16230

Material Safety Data Sheet, View in Reaxys 27 of 34

Bioassay Category

Toxicity/Safety Pharmacology

Bioassay Details

Lowest published toxic concentration;Inhalation;6 hour

Biological Species/NCBI ID

mouse

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Substance RN

1209224View in Reaxys

Substance Route of Adm.

inhalational administration

Measurement Parameter

qualitative

Qualitative value

Not Published

Material Safety Data Sheet, View in Reaxys 28 of 34

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Anesthetic pressure of the compound in mice was determined in relation to the olive-gas partition coefficient

Biological Species/NCBI ID

mouse

Substance RN

1209224View in Reaxys

Qualitative Results

log (1/p) not calculated

Measurement Parameter

qualitative

Measurement Object

log (1/p)

S.P.Gupta; Chemical reviews; vol. 89; nb. 8; (1989); p. 1765 - 1800, View in Reaxys 29 of 34

Bioassay Category

Metabolism/Transport

Bioassay Details

Partition Coefficient of the compound was determined

Substance RN

1209224View in Reaxys

Measurement Parameter

qualitative

Measurement Object

Partition coefficient

Qualitative value

Not Published

Agrawal, Vijay K.; Bano, Shahnaz; Khadikar, Padmakar V.; Bioorganic and Medicinal Chemistry; vol. 11; nb. 18; (2003); p.

4039 - 4047, View in Reaxys 30 of 34

31 of 34

Target Name

DNA

Target Synonyms

dna

Target, Subunit, Species

DNA

Target Mutant/Chimera Details

DNA:Wild

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Apparent binding constant of the compound to poly (dG.dC) DNA was evaluated by measuring the loss of ethidium fluorescence

Substance RN

1209224View in Reaxys

Qualitative Results

apparent dissociation constant (Kapp) not calculated

Measurement Parameter

qualitative

Measurement Object

apparent dissociation constant (Kapp)

Target Name

DNA

Target Synonyms

dna

Target, Subunit, Species

DNA

Target Mutant/Chimera Details

DNA:Wild

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

In Vitro (Efficacy)

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Bioassay Details

32 of 34

33 of 34

34 of 34

Apparent binding constant of the compound to Poly (dA-dT) DNA was evaluated by measuring the loss of ethidium fluorescence

Substance RN

1209224View in Reaxys

Qualitative Results

apparent dissociation constant (Kapp) not calculated

Measurement Parameter

qualitative

Measurement Object

apparent dissociation constant (Kapp)

Target Name

DNA [bovine]

Target Synonyms

dna

Target, Subunit, Species

DNA [bovine]

Target Mutant/Chimera Details

DNA [bovine]:Wild

Target Species (Bioactivity)

bovine

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Apparent binding constant of the compound to calf thymus DNA was evaluated by measuring the loss of ethidium fluorescence

Biological Species/NCBI ID

bovine

Organs/Tissues

thymus

Substance RN

1209224View in Reaxys

Qualitative Results

apparent dissociation constant (Kapp) not calculated

Measurement Parameter

qualitative

Measurement Object

apparent dissociation constant (Kapp)

Target Name

DNA

Target Synonyms

dna

Target, Subunit, Species

DNA

Target Mutant/Chimera Details

DNA:Wild

Substance Action on Target

Radioligand (/ligand)

Bioassay Category

In Vitro (Efficacy)

Bioassay Details

Apparent binding constant of the compound to T4 coliphage DNA was evaluated by measuring the loss of ethidium fluorescence

Substance RN

1209224View in Reaxys

Qualitative Results

apparent dissociation constant (Kapp) not calculated

Measurement Parameter

qualitative

Measurement Object

apparent dissociation constant (Kapp)

Substance Effect

Antioxidant

Bioassay Category

In Vitro (Efficacy)

Substance RN

1209224View in Reaxys

Measurement Parameter

IC50

Unit

Îźmol/l

Quantitative value

0.0525

Measurement pX

7.28

Copyright Š 2018 Elsevier Life Sciences IP Limited except certain content provided by third parties. Reaxys is a trademark of Elsevier Life Sciences IP Limited.

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Mousavi, Mahsa; Bakavoli, Mehdi; Shiri, Ali; Eshghi, Hossein; Journal of Heterocyclic Chemistry; vol. 55; nb. 2; (2018); p.

517 - 521, View in Reaxys

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