Nitroethane (NE; EtNO2)

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49 substances in Reaxys

2016-04-19 04h:12m:18s (EST)

1 substances in Reaxys

2016-04-19 04h:12m:39s (EST)

O N+

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Reaxys ID 1209324 View in Reaxys

O

1/1 CAS Registry Number: 79-24-3 Chemical Name: Nitroethane Linear Structure Formula: O2NCH2CH3 Molecular Formula: C2H5NO2 Molecular Weight: 75.0672 Type of Substance: acyclic InChI Key: MCSAJNNLRCFZED-UHFFFAOYSA-N Note:

N O

Substance Label (90) Label References 2a

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2

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16b

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3

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1b

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4

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3a

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36

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EtNO&2%

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2g

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31a

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12g

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48a

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7b

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l

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1e

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5b

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6b

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3b

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II

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2f

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1o

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30

Goeksu, Haydar; Ho, Sally Fae; Metin, Oender; Korkmaz, Katip; Mendoza Garcia, Adriana; Gueltekin, Mehmet Serdar; Sun, Shouheng; ACS Catalysis; vol. 4; nb. 6; (2014); p. 1777 - 1782, View in Reaxys

2h

Petkes, Hermina Iulia; Gl, Emese; Gaina, Luiza; Sabou, Mihaela; Majdik, Cornelia; Silaghi-Dumitrescu, Luminiåa; Comptes Rendus Chimie; vol. 17; nb. 10; (2014); p. 1050 - 1056, View in Reaxys

6

Li, Chunmei; Zhang, Furen; Yang, Zhen; Qi, Chenze; Tetrahedron Letters; vol. 55; nb. 40; (2014); p. 5430 - 5433, View in Reaxys

7aa

Sukhorukov, Alexey Yu.; Kapatsyna, Maria A.; Yi, Tammy Lim Ting; Park, Hyeong Ryool; Naumovich, Yana A.; Zhmurov, Petr A.; Khomutova, Yulia A.; Ioffe, Sema L.; Tartakovsky, Vladimir A.; European Journal of Organic Chemistry; vol. 2014; nb. 36; (2014); p. 8148 - 8159, View in Reaxys

EtNO2

Falorni, Massimo; Giacomelli, Giampaolo; Spanu, Emanuela; Tetrahedron Letters; vol. 39; nb. 50; (1998); p. 9241 - 9244, View in Reaxys; Kakiuchi, Takashi; Kato, Hirohide; Jayasundera, Krishanthi Padmarani; Higashi, Taijiro; Watabe, Kazuhiko; Sawamoto, Daisuke; Kinoshita, Hideki; Inomata, Katsuhiko; Chemistry Letters; nb. 10; (1998); p. 1001 - 1002, View in Reaxys; Newkome, George R.; He, Enfei; Godinez, Luis A.; Baker, Gregory R.; Chemical Communications; nb. 1; (1999); p. 27 - 28, View in Reaxys; Jones, Raymond C. F.; Bhalay, Gurdip; Carter, Paul A.; Duller, Kathryn A. M.; Dunn, Stephen H.; Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999); nb. 7; (1999); p. 765 - 776, View in Reaxys; Lucet, Denis; Sabelle, Stephane; Kostelitz, Olivier; Le Gall, Thierry; Mioskowski, Charles; European Journal of Organic Chemistry; nb. 10; (1999); p. 2583 - 2591, View in Reaxys; Lukevics; Dirnens; Pokrovska; Zicmane; Popelis; Kemme; Journal of Organometallic Chemistry; vol. 586; nb. 2; (1999); p. 200 - 207, View in Reaxys; Gallos, John K.; Koftis, Theocharis V.; Koumbis, Alexandras E.; Moutsos, Vassilios I.; Synlett; nb. 8; (1999); p. 1289 - 1291, View in Reaxys; Ranu, Brindaban C.; Hajra, Alakananda; Jana, Umasish; Synlett; nb. 1; (2000); p. 75 - 76, View in Reaxys; Hanessian, Stephen; Pham, Vinh; Organic Letters; vol. 2; nb. 19; (2000); p. 2975 - 2978, View in Reaxys; Jonsson; Loefstroem; Baeckvall; Journal of Organic Chemistry; vol. 65; nb. 25; (2000); p. 8454 - 8457, View in Reaxys; El Hadri; Nicolle; Guillaume; Leclerc; Pietri-Rouxel; Strosberg; Archimbault; Pharmazie; vol. 56; nb. 7; (2001); p. 517 - 522, View in Reaxys; Han; Lee; Mi; Park; Angerhofer; Cordell; Kim; Journal of Natural Products; vol. 64; nb. 9; (2001); p. 1201 - 1205, View in Reaxys; Uno, Hidemitsu; Kitawaki, Yukiko; Ono, Noboru; Chemical Communications; nb. 2; (2002); p. 116 - 117, View in Reaxys; Fujii, Akihito; Fujima, Yoshito; Harada, Hiroshi; Ikunaka, Masaya; Inoue, Toru; Kato, Shiro; Matsuyama, Keisuke; Tetrahedron Asymmetry; vol. 12; nb. 23; (2001); p. 3235 - 3240, View in Reaxys; Denmark, Scott E.; Gomez, Laurent; Heterocycles; vol. 58; (2002); p. 129 - 136, View in Reaxys; Klein, Guenter; Pandiaraju, Subramaniam; Reiser, Oliver; Tetrahedron Letters; vol. 43; nb. 42; (2002); p. 7503 - 7506, View in Reaxys; Trachsel, Daniel; Helvetica Chimica Acta; vol. 85; nb. 9; (2002); p. 3019 - 3026, View in Reaxys; Roy, Amrendra K.; Batra, Sanjay; Synthesis; nb. 9; (2003); p. 1347 - 1356, View in Reaxys; Giacomelli, Giampaolo; De Luca, Lidia; Porcheddu, Andrea; Tetrahedron; vol. 59; nb. 29; (2003); p. 5437 - 5440, View in Reaxys; Andrey, Olivier; Vidonne, Annick; Alexakis, Alexandre; Tetrahedron Letters; vol. 44; nb.

43; (2003); p. 7901 - 7904, View in Reaxys; Denmark, Scott E.; Gomez, Laurent; Journal of Organic Chemistry; vol. 68; nb. 21; (2003); p. 8015 - 8024, View in Reaxys; Khan, Faiz Ahmed; Dash, Jyotirmayee; Satapathy, Rashmirekha; Upadhyay, Sarasij K.; Tetrahedron Letters; vol. 45; nb. 15; (2004); p. 3055 - 3058, View in Reaxys; Rosso, Giovanni B.; Pilli, Ronaldo A.; Tetrahedron Letters; vol. 47; nb. 2; (2006); p. 185 188, View in Reaxys; Addo, James K.; Teesdale-Spittle, Paul; Hoberg, John O.; Synthesis; nb. 12; (2005); p. 1923 - 1925; Art.No: M09404SS, View in Reaxys; Siu, Jason; Baxendale, Ian R.; Lewthwaite, Russell A.; Ley, Steven V.; Organic and Biomolecular Chemistry; vol. 3; nb. 17; (2005); p. 3140 - 3160, View in Reaxys; Mitchell, Claire E. T.; Brenner, Stacey E.; Garcia-Fortanet, Jorge; Ley, Steven V.; Organic and Biomolecular Chemistry; vol. 4; nb. 10; (2006); p. 2039 - 2049, View in Reaxys; Oriyama, Takeshi; Aoyagi, Masaru; Iwanami, Katsuyuki; Chemistry Letters; vol. 36; nb. 5; (2007); p. 612 - 613,

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48; nb. 32; (2007); p. 5653 - 5656, View in Reaxys; Gree, Danielle; Gree, Rene; Tetrahedron Letters; vol.

48; nb. 31; (2007); p. 5435 - 5438, View in Reaxys; Singh, Vijay; Batra, Sanjay; European Journal of Organic Chemistry; nb. 18; (2007); p. 2970 - 2976, View in Reaxys; Parker, Matthew A.; Kurrasch, Deborah M.; Nichols, David E.; Bioorganic and Medicinal Chemistry; vol. 16; nb. 8; (2008); p. 4661 - 4669, View in Reaxys; Zhmurov; Tabolin; Sukhorukov; Lesiv; Klenov; Khomutova; Ioffe; Tartakovsky; Russian Chemical Bulletin; vol. 60; nb. 11; (2011); p. 2390 - 2395, View in Reaxys; Boobalan, Ramalingam; Lee, Gene-Hsian; Chen, Chinpiao; Advanced Synthesis and Catalysis; vol. 354; nb. 13; (2012); p. 2511 - 2520, View in Reaxys; Keiko, Natalia A.; Aksamentova, Tamara N.; Chipanina, Nina N.; Verochkina, Ekaterina A.; Vchislo, Nadezhda V.; Tetrahedron; vol. 69; nb. 8; (2013); p. 2022 - 2032, View in Reaxys; Coste, Alexis; Kim, Justin; Adams, Timothy C.; Movassaghi, Mohammad; Chemical Science; vol. 4; nb. 8; (2013); p.

3191 - 3197, View in Reaxys 4b

Okino, Tomotaka; Nakamura, Satoru; Furukawa, Tomihiro; Takemoto, Yoshiji; Organic Letters; vol. 6; nb. 4; (2004); p. 625 - 627, View in Reaxys; Uraguchi, Daisuke; Sakaki, Sawako; Ooi, Takashi; Journal of the American Chemical Society; vol. 129; nb. 41; (2007); p. 12392 - 12393, View in Reaxys; Zu, Liansuo; Xie, Hexin; Li, Hao; Wang, Jian; Wang, Wei; Advanced Synthesis and Catalysis; vol. 349; nb. 17-18; (2007); p. 2660 - 2664, View in Reaxys; Patent; Mitsui Chemicals, Inc.; National University Corporation Nagoya University; US2009/131716; (2009); (A1) English, View in Reaxys; Dhineshkumar, Jayaraman; Lamani, Manjunath; Alagiri, Kaliyamoorthy; Prabhu, Kandikere Ramaiah; Organic Letters; vol. 15; nb. 5; (2013); p. 1092 - 1095, View in Reaxys; Wang, Hong-Yu; Chai, Zhuo; Zhao, Gang; Tetrahedron; vol. 69; nb. 25; (2013); p. 5104 - 5111, View in Reaxys; Piscopo, Calogero G.; Sartori, Giovanni; Mayoral, Jose A.; Lanari, Daniela; Vaccaro, Luigi; Maggi, Raimondo; Synlett; vol. 24; nb. 19; (2013); p. 2596 - 2600; Art.No: ST-2013-D0688-L, View in Reaxys

35a

Kancharla, Papireddy; Reynolds, Kevin A.; Tetrahedron; vol. 69; nb. 39; (2013); p. 8375 - 8385, View in Reaxys

9b

Lancianesi, Stefano; Palmieri, Alessandro; Petrini, Marino; Advanced Synthesis and Catalysis; vol. 355; nb. 16; (2013); p. 3285 - 3289, View in Reaxys

1b; EtNO&2%

Quintavalla, Arianna; Lanza, Francesco; Montroni, Elisa; Lombardo, Marco; Trombini, Claudio; Journal of Organic Chemistry; vol. 78; nb. 23; (2013); p. 12049 - 12064, View in Reaxys

8a

Janecki, Tomasz; Blaszczyk, Edyta; Studzian, Kazimierz; Janecka, Anna; Krajewska, Urszula; Rozalski, Marek; Journal of Medicinal Chemistry; vol. 48; nb. 10; (2005); p. 3516 - 3521, View in Reaxys; Deng, Yan-Qiu; Zhang, Zhen-Wei; Feng, Ya-Hui; Chan, Albert S.C.; Lu, Gui; Tetrahedron Asymmetry; vol. 23; nb. 24; (2012); p. 1647 - 1652, View in Reaxys

9

Zhou, Yirong; Liu, Qiang; Gong, Yuefa; Organic and Biomolecular Chemistry; vol. 10; nb. 37; (2012); p.

7618 - 7627, View in Reaxys

b

Fioravanti, Stefania; Marchetti, Fabio; Pellacani, Lucio; Ranieri, Luca; Tardella, Paolo A.; Tetrahedron Asymmetry; vol. 19; nb. 2; (2008); p. 231 - 236, View in Reaxys

4a

Poupart; Fazal; Goulet; Ly Thy Mar; Journal of Organic Chemistry; vol. 64; nb. 4; (1999); p. 1356 - 1361, View in Reaxys; Handa, Shinya; Nagawa, Keita; Sohtome, Yoshihiro; Matsunaga, Shigeki; Shibasaki, Masakatsu; Angewandte Chemie - International Edition; vol. 47; nb. 17; (2008); p. 3230 - 3233, View in Reaxys

6a

Zhang, Qian; Sun, Shaoguang; Hu, Jianglei; Liu, Qun; Tan, Jing; Journal of Organic Chemistry; vol. 72; nb. 1; (2007); p. 139 - 143, View in Reaxys

23G

Takemoto, Yoshiji; Miyabe, Hideto; Chimia; vol. 61; nb. 5; (2007); p. 269 - 275, View in Reaxys

6, R1 = Me

Letourneau, Jeffrey J.; Riviello, Christopher; Ohlmeyer, Michael H.J.; Tetrahedron Letters; vol. 48; nb.

10; (2007); p. 1739 - 1743, View in Reaxys

MeCH2NO2

Caldarelli, Marina; Habermann, Joerg; Ley, Steven V.; Journal of the Chemical Society - Perkin Transactions 1; nb. 2; (1999); p. 107 - 110, View in Reaxys; Gallos, John K.; Koftis, Theocharis V.; Journal of the Chemical Society. Perkin Transactions 1; nb. 4; (2001); p. 415 - 423, View in Reaxys; Filho, Joao R. de Freitas; Cottier, Louis; Srivastava, Rajendra M.; Sinou, Denis; Synlett; nb. 9; (2003); p. 1358 - 1360, View in Reaxys; Chang, Yu-Wei; Yang, Jing-Jun; Dang, Jin-Ning; Xue, Yue-Xia; Synlett; nb. 14; (2007); p.

2283 - 2285, View in Reaxys

10

Campana, Araceli G.; Fuentes, Noelia; Gomez-Bengoa, Enrique; Mateo, Cristina; Oltra, J. Enrique; Echavarren, Antonio M.; Cuerva, Juan M.; Journal of Organic Chemistry; vol. 72; nb. 21; (2007); p. 8127 8130, View in Reaxys

CH3CH2NO2

Kawakami; Suzuki; Tetrahedron Letters; vol. 40; nb. 6; (1999); p. 1157 - 1160, View in Reaxys; Liebeschuetz; Katz; Duriatti; Arnold; Pesticide Science; vol. 50; nb. 3; (1997); p. 258 - 274, View in Reaxys; Arnold, Mary L.; Duriatti, Albert D.; Jung, Michel; Katz, Ruth B.; Liebeschuetz, John W.; Pesticide Science; vol. 44; nb. 4; (1995); p. 341 - 356, View in Reaxys; Chamakh, Ahlem; M'hirsi, Mustapha; Villieras, Jean; Lebreton, Jacques; Amri, Hassen; Synthesis; nb. 2; (2000); p. 295 - 299, View in Reaxys; Yashiro; Nishida; Kobayashi; Ohno; Synlett; nb. 3; (2000); p. 361 - 362, View in Reaxys; Simoni, Daniele; Ronda-

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nin, Riccardo; Morini, Massimo; Baruchello, Riccardo; Invidiata, Francesco Paolo; Tetrahedron Letters; vol. 41; nb. 10; (2000); p. 1607 - 1610, View in Reaxys; Xu, Ping; Lin, Wenwei; Zou, Xiaomin; Synthesis; nb. 8; (2002); p. 1017 - 1026, View in Reaxys; Velmathi; Swarnalakshmi; Narasimhan; Tetrahedron Asymmetry; vol. 14; nb. 1; (2003); p. 113 - 117, View in Reaxys; Bocharov, Semyon; Mathauser, Anna T.; Teplyakov, Andrew V.; Journal of Physical Chemistry B; vol. 107; nb. 31; (2003); p. 7776 - 7782, View in Reaxys; Jiao; DeJoseph Jr.; Garscadden; Journal of Physical Chemistry A; vol. 107; nb. 42; (2003); p. 9040 - 9044, View in Reaxys; Liu, Hong-Min; Zhang, Fuyi; Zou, Da-Peng; Chemical Communications; nb. 16; (2003); p. 2044 - 2045, View in Reaxys; Dominguez, Rosa Maria; Herize, Armando; Rotinov, Alexandra; Alvarez-Aular, Alvaro; Visbal, Gonzalo; Chuchani, Gabriel; Journal of Physical Organic Chemistry; vol. 17; nb. 5; (2004); p. 399 - 408, View in Reaxys; Lee, Anna; Kim, Woosung; Lee, Jinwoo; Hyeon, Taeghwan; Kim, B. Moon; Tetrahedron Asymmetry; vol. 15; nb. 17; (2004); p. 2595 - 2598, View in Reaxys; Ranu, Brindaban C.; Banerjee, Subhash; Organic Letters; vol. 7; nb. 14; (2005); p. 3049 3052, View in Reaxys; Dahnz, Axel; Helmchen, Guenter; Synlett; nb. 5; (2006); p. 697 - 700, View in Reaxys; O'Leary, Jane; Formosa, Xavier; Skranc, Wolfgang; Wallis, John D.; Organic and Biomolecular Chemistry; vol. 3; nb. 18; (2005); p. 3273 - 3283, View in Reaxys; Cecchi, Luca; De Sarlo, Francesco; Machetti, Fabrizio; Synlett; nb. 15; (2007); p. 2451 - 2453, View in Reaxys educt to 3

Liu, Feng-Wu; Yan, Lin; Zhang, Jing-Yu; Liu, Hong-Min; Carbohydrate Research; vol. 341; nb. 3; (2006); p. 332 - 338, View in Reaxys

2b-H

Thanh, Binh Phan; Mayr, Herbert; European Journal of Organic Chemistry; nb. 11; (2006); p. 2530 - 2537, View in Reaxys

4 (R2=Et)

Ballini, Roberto; Clemente, Roberto Rabanedo; Palmieri, Alessandro; Petrini, Marino; Advanced Synthesis and Catalysis; vol. 348; nb. 1-2; (2006); p. 191 - 196, View in Reaxys

educt to 2a,b

Park, Da Yeon; Gowrisankar, Saravanan; Kim, Jae Nyoung; Tetrahedron Letters; vol. 47; nb. 37; (2006); p. 6641 - 6645, View in Reaxys

educt to 4a-4l

Lu, Shao-Feng; Du, Da-Ming; Xu, Jiaxi; Zhang, Shi-Wei; Journal of the American Chemical Society; vol.

128; nb. 23; (2006); p. 7418 - 7419, View in Reaxys

11

Jin, Young Lee; Hong, Young-Taek; Kim, Sunggak; Angewandte Chemie - International Edition; vol. 45; nb. 37; (2006); p. 6182 - 6186, View in Reaxys

15

Black, Phillip. J.; Cami-Kobeci, Gerta; Edwards, Michael G.; Slatford, Paul A.; Whittlesey, Michael K.; Williams, Jonathan M. J.; Organic and Biomolecular Chemistry; vol. 4; nb. 1; (2006); p. 116 - 125, View in Reaxys

3c

Xu, Xuenong; Furukawa, Tomihiro; Okino, Tomotaka; Miyabe, Hideto; Takemoto, Yoshiji; Chemistry - A European Journal; vol. 12; nb. 2; (2006); p. 466 - 476, View in Reaxys

1, R1 = Me

Ballini, Roberto; Barboni, Luciano; Bosica, Giovanna; Filippone, Paolino; Peretti, Sabina; Tetrahedron; vol. 56; nb. 24; (2000); p. 4095 - 4099, View in Reaxys; Elmaaty, Tarek Abou; Castle, Lyle W.; Organic Letters; vol. 7; nb. 24; (2005); p. 5529 - 5530, View in Reaxys

Tab. 2

Veldurthy, Bhaskar; Clacens, Jean Marc; Figueras, Francois; Advanced Synthesis and Catalysis; vol.

347; nb. 6; (2005); p. 767 - 771, View in Reaxys

ANC; R1=R2=H

Sukhorokov, Alexey Yu.; Bliznets, Igor V.; Lesiv, Alexey V.; Khomutova, Yulija A.; Strelenko, Yuriy A.; Ioffe, Sema L.; Synthesis; nb. 7; (2005); p. 1077 - 1082; Art.No: P14804SS, View in Reaxys

2i

Ooi, Takashi; Fujioka, Shingo; Maruoka, Keiji; Journal of the American Chemical Society; vol. 126; nb. 38; (2004); p. 11790 - 11791, View in Reaxys

1b-H (R1=H, R2=CH3)

Bug, Thorsten; Lemek, Tadeusz; Mayr, Herbert; Journal of Organic Chemistry; vol. 69; nb. 22; (2004); p.

7565 - 7576, View in Reaxys

7a

Blaszczyk, Edyta; Krawczyk, Henryk; Janecki, Tomasz; Synlett; nb. 15; (2004); p. 2685 - 2688, View in Reaxys

2a,2b

Ghosh, Tarun; Bandyopadhyay, Chandrakanta; Tetrahedron Letters; vol. 45; nb. 32; (2004); p. 6169 6172, View in Reaxys

1, R=CH3

Ballini, Roberto; Bosica, Giovanna; Livi, Damiana; Palmieri, Alessandro; Maggi, Raimondo; Sartori, Giovanni; Tetrahedron Letters; vol. 44; nb. 11; (2003); p. 2271 - 2273, View in Reaxys

2e

Jousse-Karinthi, Celine; Zouhiri, Fatima; Mahuteau, Jacqueline; Desmaele, Didier; Tetrahedron; vol. 59; nb. 12; (2003); p. 2093 - 2099, View in Reaxys

2 (R&3%=H)

Chimichi, Stefano; Boccalini, Marco; Cosimelli, Barbara; Dall'Acqua, Francesco; Viola, Giampietro; Tetrahedron; vol. 59; nb. 28; (2003); p. 5215 - 5223, View in Reaxys

1, R = CH3

Ballini, Roberto; Barboni, Luciano; Giarlo, Guido; Journal of Organic Chemistry; vol. 68; nb. 23; (2003); p.

9173 - 9176, View in Reaxys

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R3CH2NO2, R3=CH3

Pathak, Rashmi; Shaw, Arun K.; Bhaduri, Amiya P.; Chandrasekhar; Srivastava, Anil; Srivastava, Kishore K.; Chaturvedi, Vineeta; Srivastava, Ranjana; Srivastava, Brahm S.; Arora, Shalini; Sinha, Sudhir; Bioorganic and Medicinal Chemistry; vol. 10; nb. 6; (2002); p. 1695 - 1702, View in Reaxys

nitro compd educt El Kaim; Grimaud; Jana; Tirla; Tetrahedron Letters; vol. 43; nb. 11; (2002); p. 2037 - 2038, View in Reaxys to 1a 11b

Tranmer, Geoffrey K.; Tam, William; Organic Letters; vol. 4; nb. 23; (2002); p. 4101 - 4104, View in Reaxys

1c

Dilman; Lyapkalo; Ioffe; Strelenko; Tartakovsky; Synthesis; nb. 10; (1999); p. 1767 - 1775, View in Reaxys; Halland, Nis; Hazell, Rita G.; Jorgensen, Karl Anker; Journal of Organic Chemistry; vol.

67; nb. 24; (2002); p. 8331 - 8338, View in Reaxys

12

Nishiwaki, Yoshiki; Sakaguchi, Satoshi; Ishii, Yasutaka; Journal of Organic Chemistry; vol. 67; nb. 16; (2002); p. 5663 - 5668, View in Reaxys

C2H5NO2

Iki, Nobuhiko; Suzuki, Takehiro; Koyama, Katsuyoshi; Kabuto, Chizuko; Miyano, Sotaro; Organic Letters; vol. 4; nb. 4; (2002); p. 509 - 512, View in Reaxys

3g

Djekou, Serge; Gellis, Armand; Maldonado, Jose; Crozet, Michel P.; Vanelle, Patrice; Heterocycles; vol.

55; nb. 3; (2001); p. 535 - 544, View in Reaxys

educt to IIIa

Bondar'; Koval'skaya; Skupskaya; Pashkovskii; Dikusar; Kozlov; Lakhvich; Russian Journal of Organic Chemistry; vol. 37; nb. 1; (2001); p. 23 - 28, View in Reaxys

2, R=Me

Demicheli, Giuseppina; Maggi, Raimondo; Mazzacani, Alessandro; Righi, Paolo; Sartori, Giovanni; Bigi, Franca; Tetrahedron Letters; vol. 42; nb. 12; (2001); p. 2401 - 2403, View in Reaxys

educt to III

Pashkovskii; Lakhvich; Koval'skaya; Kozlov; Russian Journal of Organic Chemistry; vol. 37; nb. 3; (2001); p. 375 - 381, View in Reaxys

starting to 1e-g

Dumez, Estelle; Faure, Robert; Dulcere, Jean-Pierre; European Journal of Organic Chemistry; nb. 13; (2001); p. 2577 - 2588, View in Reaxys

2c

Nishiwaki, Nagatoshi; Knudsen, Kristian Rahbek; Gothelf, Kurt V.; Jrgensen, Karl Anker; Angewandte Chemie - International Edition; vol. 40; nb. 16; (2001); p. 2992 - 2995, View in Reaxys

EtNO2; CH3CH2NO2

Xu; Singh; Gopal; Sayre; Chemical Research in Toxicology; vol. 14; nb. 3; (2001); p. 264 - 274, View in Reaxys

2, R1 = CH3

Beji, Feten; Lebreton, Jacques; Villieras, Jean; Amri, Hassen; Tetrahedron; vol. 57; nb. 50; (2001); p.

9959 - 9962, View in Reaxys

h5-nitroethane

De Sousa, Herminio C.; Rebelo, Luis P. N.; Journal of Chemical Thermodynamics; vol. 32; nb. 3; (2000); p.

355 - 387, View in Reaxys

3, R=Me, R1=H

Ballini, Roberto; Barboni, Luciano; Bosica, Giovanna; Petrini, Marino; Synlett; nb. 3; (2000); p. 391 393, View in Reaxys

RCH2NO2, R=CH3

Terme, Thierry; Crozet, Michel P.; Giraud, Luc; Vanelle, Patrice; Tetrahedron; vol. 56; nb. 8; (2000); p.

1097 - 1101, View in Reaxys

2y

Ballini, Roberto; Bigi, Franca; Gogni, Elena; Maggi, Raimondo; Sartori, Giovanni; Journal of Catalysis; vol. 191; nb. 2; (2000); p. 348 - 353, View in Reaxys

1, R=Me

Youn, So Won; Kim, Yong Hae; Synlett; nb. 6; (2000); p. 880 - 882, View in Reaxys

educt to 6e

Vanelle; Terme; Crozet; Tetrahedron Letters; vol. 41; nb. 33; (2000); p. 6383 - 6385, View in Reaxys

NE

Choudary; Lakshmi Kantam; Kavita; Venkat Reddy; Figueras; Tetrahedron; vol. 56; nb. 47; (2000); p.

9357 - 9364, View in Reaxys

educt to 11

Kamal, Marwan R.; El-Abadelah, Mustafa M.; Mohammad, Amer A.; Meier, Herbert; Heterocycles; vol.

50; nb. 2; (1999); p. 819 - 832, View in Reaxys

1, R1=Me, R2=H

Sebti, Said; Boukhal, Hassan; Hanafi, Naima; Boulaajaj, Said; Tetrahedron Letters; vol. 40; nb. 34; (1999); p. 6207 - 6209, View in Reaxys

O2NCH2CH3

Lee, Shi Yong; Lee, Bum Sung; Oh, Dong Young; Synthesis; nb. 12; (1999); p. 2027 - 2029, View in Reaxys

1a,b,f,g,n

Ballini, Roberto; Bosica, Giovanna; Parrini, Mauro; Tetrahedron Letters; vol. 39; nb. 43; (1998); p. 7963 7964, View in Reaxys

Patent-Specific Data (7) Prophetic ComLocation in Patent References pound

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Patent; Richter Gedeon Nyrt.; Beke, Gyula; Bényei, Gyula Attila; Borza, István; Bozó, Éva; Farkas, Sándor; Hornok, Katalin; Papp, Andrea; Vágó, István; Vastag, Mónika; US2013/217702; (2013); (A1) English, View in Reaxys; Patent; Pusan National University Indusrtyuniversity; Chung, Hae Young; Park, Min Hi; Ha, Young Mi; Han, Yu Kyeong; Park, Ji Young; Park, Yun Jung; Kim, Jin Ah; Lee, Ji Yeon; Song, Yu Min; Moon, Hyung Ryong; US2014/37564; (2014); (A1) English, View in Reaxys; Patent; NOVARTIS AG; Bock, Mark Gary; Gaul, Christoph; Gummadi, Venkateshwar Rao; Moebitz, Henrik; Sengupta, Saumitra; US2014/45872; (2014); (A1) English, View in Reaxys; Patent; Institute For Applied Cancer Science/The University of Texas MD Anderson Cancer Center; Jones, Philip; DiFrancesco, Maria Emilia; Petrocchi, Alessia; Marszalek, Joe; Liu, Gang; US2014/57914; (2014); (A1) English, View in Reaxys; Patent; SCHUNK, Stefan; REICH, Melanie; STEINHAGEN, Henning; DAMANN, Nils; HAURAND, Michael; KLESS, Achim; SKONE, Philip; HAMLYN, Richard; KIRBY, Robert; ROGERS, Marc; SUTTON, Kathy; US2014/66426; (2014); (A1) English, View in Reaxys; Patent; Caldwell, Richard D.; GUCKIAN, Kevin M.; KUMARA VEL, Gnanasambandam; LEE, Wen-Cherng; LIN, Edward Yin-Shiang; LlU, Xiaogao; MA, Bin; SCOTT, Daniel M.; SHl, Zhan; THOMAS, Jermaine; TAVERAS, Arthur G.; ZHENG, Guo Zhu; US2014/100195; (2014); (A1) English, View in Reaxys; Patent; NOVARTIS AG; Fairhurst, Robin Alec; Furet, Pascal; Kalthoff, Frank Stephan; Lerchner, Andreas; Rueeger, Heinrich; US2014/135330; (2014); (A1) English, View in Reaxys; Patent; CHIRON A/S; Johansen, Jon Eigill; Liu, Huiling; Karlsen, Morten; US2014/227792; (2014); (A1) 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; Trauth, Daniel M.; Green, George D.; Swedo, Raymond J.; US2011/92750; (2011); (A1) English, View in Reaxys

Claim

Patent; Lister, Tedd Edward; Fox, Robert Vincent; US2009/38953; (2009); (A1) English, View in Reaxys Patent; UNIBAN - Universidade Bandeirante de Sao Paulo - Academia Paulista Anchieta S/C LTDA; FAPESP - Fundacao de Amparo a Pesquisa do Estado de Sao Paulo; WO2008/3155; (2008); (A2) English, View in Reaxys Patent; Niewohner, Ulrich; Niewohner, Maria; Bauser, Marcus; Erguden, Jens-Kerim; Flubacher, Dietmar; Naab, Paul; Repp, Thorsten-Oliver; Stoltefuss, Jurgen; Burkhardt, Nils; Sewing, Andrea; Schauer, Michael; Schlemmer, Karl-Heinz; Weber, Olaf; Boyer, Stephen J.; Miglarese, Mark; Fan, Jianmei; Phillips, Barton; Raudenbush, Brian C.; Wang, Yamin; US2003/236276; (2003); (A1) English, View in Reaxys

prophetic product

prophetic product

Patent; Eli Lilly and Company; US4303591; (1981); (A1) English, View in Reaxys; Patent; Mitsui Toatsu Chemicals, Inc.; US5536878; (1996); (A1) English, View in Reaxys; Patent; Mitsui Toatsu Chemicals, Incorporated; US5382690; (1995); (A1) English, View in Reaxys Claim

Patent; Berg; Lloyd; US5425854; (1995); (A1) English, View in Reaxys

Related Structure (3) Related Structure Referenced Com- References pound The following tau- acetohydroxamic tomers are disacid cussed: /BRN= 1848014/

Veltwisch, Dieter; Asmus, Klaus-Dieter; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1982); p. 1143 - 1146, View in Reaxys Bogolyubov et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 41; (1971); p.

1311,1320,1321,1322, View in Reaxys; Witanowski; Journal of the American Chemical Society; vol. 90; (1968); p. 5683, View in Reaxys

Man fasst die freie Verbindung als wahres Nitraethan auf und leitet ihr Salze von der Isonitro-Form ab.

Derivative (22) Comment (Derivative) Li-Nitroaethanid 5: Rk. mit α-t-Bu-

Beilstein Handbook, View in Reaxys

References Norris,R.K.; Randles,D.; Australian Journal of Chemistry; vol. 32; (1979); p. 1487 - 1509, View in Reaxys

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tylchlorid 3; Rk. mit α-Isopropylverb. 2; Rk. mit αChloroaethylbenzol: Produktverteilung Carbanion, Rkt.m.flavinhaltigen Polymeren u.Isoalloxazinen (-->k2 (Tab.II), E1/2 (Tab.II))

Shinkai et al.; Biopolymers; vol. 17; (1978); p. 2757,2758,2759, View in Reaxys

Addukt mit IIIc: UV (S.6723)

Chan,R.L.; Bruice,T.C.; Journal of the American Chemical Society; vol. 99; (1977); p. 6721 - 6730, View in Reaxys

Na-Salz Odokienko et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 47; (1974); p. 902,919, View in Reaxys NaC2H4NO2, Loesungswaerme in W. u. D2O, Isotopeneffekt Na-Salz: 1H-NMR Lorberth; Lange; Journal of Organometallic Chemistry; vol. 54; (1973); p. 165,167, 170, View in Reaxys (S.169) Komplex m. Triaethylamin: UV; IR; gelb

Mayahi; Al-Baldawi; Journal of the Indian Chemical Society; vol. 48; (1971); p. 1171, View in Reaxys

d. Na-Salzes: Rk. m. 2-Chlorvinylphenylketon

Belyaev; Prokopovich; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 1599,1661, View in Reaxys

K+-Salz: IR; UV

Fukuyama,M. et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 4689 - 4699, View in Reaxys

Li+-Salz: IR; UV

Fukuyama,M. et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 4689 - 4699, View in Reaxys

Na+-Salz: IR; UV

Fukuyama,M. et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 4689 - 4699, View in Reaxys

<CH3CHNO2>Na+: NMR

Witanowski; Shevelev; Journal of Molecular Spectroscopy; vol. 33; (1970); p. 19,20, View in Reaxys

Natrium-Salz: IRu. Raman-Sp.

Brookes; Jonathan; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 187,188, View in Reaxys

Na-Salz : Rk. mit Perfluor-isobutylen

Koshtoyan,S.O. et al.; Doklady Chemistry; vol. 185; (1969); p. 285 - 287; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 185; (1969); p. 837 - 839, View in Reaxys

Na-Salz: IR-Sp. (KBr); UV-Sp.; NMR-Sp.

Griswold,A.A.; Starcher,P.S.; Journal of Organic Chemistry; vol. 30; (1965); p. 1687 - 1690, View in Reaxys

Na-Salz: Rk. mit Kornblum,N.; Brown,R.A.; Journal of the American Chemical Society; vol. 86; (1964); p. 2681 - 2687, Trimethyl- bzw.

View in Reaxys Triethyloxoniumborfluorid in Methylenchlorid (-60grad, N2) -> Methyl- bzw. Ethylester der Nitronsaeure von Nitroethan; aehnliche Rk. mit NaSalzen von aehnlichen Nitro-organischen Verbindungen Na-Salz: charakter. IR-Banden

Feuer,H. et al.; Spectrochimica Acta; vol. 19; (1963); p. 431 - 434, View in Reaxys

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Na-Salz: Rk. mit Kornblum,N.; Brown,R.A.; Journal of the American Chemical Society; vol. 85; (1963); p. 1359 - 1360, Triethyloxonium- View in Reaxys fluorborat in Methylenchlorid (N2, 0grad, 15 min) -> Ethylidennitronsaeure-ethylester Na-Salz: Rk. mit Kornblum,N.; Brown,R.A.; Journal of the American Chemical Society; vol. 85; (1963); p. 1359 - 1360, TrimethyloxoView in Reaxys niumfluorborat in Methylenchlorid (N2, 0grad, 15 min) -> Ethylidennitronsaeuremethylester Komplexbildung mit versch. Aromaten, Gleichgew.-Konst. (Tab. 1)

Anderson et al.; AIChE Journal; vol. 8; (1962); p. 66,67, View in Reaxys

Na-Salz Buczkowski; Urbanski; Spectrochimica Acta; vol. 18; (1962); p. 1187,1188, View in Reaxys NaC2H4NO2: aus Nitroethan in A. u.

Natriumethylat; IR-Sp.(1750-600 cm-1) as 1-nitro-acetaldehyde-<4-nitrophenylhydrazone>(mp: 157 degree >

Slebodzinski; Makaruk; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. <III> 3; (1955); p. 377,379, View in Reaxys

silver salt; Further Angeli; Alessandri; Atti della Accademia Nazionale dei Lincei, Classe di Scienze Fisiche, Matematiche e Data see HandNaturali, Rendiconti; vol. <5> 19 I; (1910); p. 787, View in Reaxys book (Preparation, Chemical Behaviour) Melting Point (2) 1 of 2

Melting Point [°C]

-89.52

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 2 of 2

Melting Point [°C]

-90

Gabriel; Industrial and Engineering Chemistry; vol. 32; (1940); p. 891, View in Reaxys Boiling Point (22) Boiling Point [°C] Pressure (Boiling Point) [Torr] 112 - 116

Location

References

Page/Page column 13

Patent; CHEVRON PHILLIPS CHEMICAL COMPANY LP; US2010/256391; (2010); (A1) English, View in Reaxys

110 - 114

Zarchi, Mohammad Ali Karimi; Zarei, Amin; Journal of the Chinese Chemical Society; vol. 52; nb. 2; (2005); p. 309 - 311, View in Reaxys

114

760

Kuznetsova, I. I.; Bazanov, A. G.; Tselinskii, I. V.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 4; (1980); p. 619 - 625; Zhurnal Organicheskoi Khimii; vol. 16; nb. 4; (1980); p.

707 - 713, View in Reaxys

111

760

Munz,R.; Simchen,G.; Liebigs Annalen der Chemie; (1979); p. 628 638, View in Reaxys

114

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p.

73,74, View in Reaxys; Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1210,1194,1195,1196,1197, View in Reaxys

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112.35 - 113.35

Szilagyi et al; Acta Physica et Chemica; vol. 21; (1975); p. 137,138, 141, View in Reaxys

114.8 - 115

Hand; Jencks; Journal of the American Chemical Society; vol. 97; (1975); p. 6221,6223, View in Reaxys

113

Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p.

379, View in Reaxys

114 - 115

Bell, Cox; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 783, View in Reaxys

114 - 115

760

Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p.

1284,1287, View in Reaxys

60

113

Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 315, View in Reaxys

71

210

Pikhl et al.; Organic Reactivity (New York, English Translation); vol.

3; (1966); p. 297,298, View in Reaxys

114.15

Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys

114.5

761

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p.

187,188, View in Reaxys

48.2

80

Andrussow; Zeitschrift fuer Physikalische Chemie (Leipzig); vol.

208; (1958); p. 78,93, View in Reaxys

114.07

760

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

81.5 - 82

263

Hurdis; Smyth; Journal of the American Chemical Society; vol. 64; (1942); p. 2832, View in Reaxys

65.6

153

Hurdis; Smyth; Journal of the American Chemical Society; vol. 64; (1942); p. 2832, View in Reaxys

114

760

Hodge; Industrial and Engineering Chemistry; vol. 32; (1940); p.

748, View in Reaxys

115

760

Hass; Hodge; Vanderbilt; Industrial and Engineering Chemistry; vol. 28; (1936); p. 341, View in Reaxys

114 - 114.8

760.7

Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 567, View in Reaxys

113 - 114

737.1

Meyer,V.; Justus Liebigs Annalen der Chemie; vol. 171; (1874); p.

19; Justus Liebigs Annalen der Chemie; vol. 175; (1875); p. 88, View in Reaxys

Refractive Index (25) Refractive Index Wavelength (Refractive Index) [nm]

Temperature (Refractive Index) [°C]

References

1.3896

589

25

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys

1.3916

589

20

Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p.

1284,1287, View in Reaxys; Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 315, View in Reaxys; Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys

1.3897

589

25

Uosaki, Yasuhiro; Mutsumura, Hajime; Wakasa, Shinji; Moriyoshi, Takahashi; Journal of Chemical Thermodynamics; vol. 22; nb. 3; (1990); p. 313 - 318, View in Reaxys

1.39

589

20

Kuznetsova, I. I.; Bazanov, A. G.; Tselinskii, I. V.; Journal of Organic Chemistry USSR (English Translation); vol. 16; nb. 4; (1980); p. 619 - 625; Zhurnal Organicheskoi Khimii; vol. 16; nb. 4; (1980); p.

707 - 713, View in Reaxys

1.3895

589

25

Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys; Hsu; Clever; Journal of

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Chemical and Engineering Data; vol. 20; (1975); p. 268,269 - 271, View in Reaxys 1.3905

589

20

Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1210,1194,1195,1196,1197, View in Reaxys

1.3893

589

25

Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p.

379, View in Reaxys

1.3912

589

20

Bahurel et al.; Bulletin de la Societe Chimique de France; (1971); p.

2331,2336, View in Reaxys Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p.

3728, View in Reaxys

1.3928

589

20

Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p.

73,74, View in Reaxys

1.3898

589

20

Pikhl et al.; Organic Reactivity (New York, English Translation); vol.

3; (1966); p. 297,298, View in Reaxys

1.392

589

20

Williams et al.; Journal of Organic Chemistry; vol. 30; (1965); p.

2674,2675, View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys

1.3789

589

50

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p.

187,188, View in Reaxys

1.3901

589

25

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p.

187,188, View in Reaxys

1.3921

589

20

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p.

187,188, View in Reaxys

1.39193

589

20

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

1.38973

589

25

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

1.38754

589

30

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

1.3917

589

20

Gabriel; Industrial and Engineering Chemistry; vol. 32; (1940); p.

891, View in Reaxys; Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys; Hurdis; Smyth; Journal of the American Chemical Society; vol. 64; (1942); p. 2832, View in Reaxys; Vogel; Journal of the Chemical Society; (1948); p.

1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.3894

656.3

20

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.3977

486.1

20

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.4021

434

20

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

1.38768

656.3

24.3

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

24.3

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

24.3

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys

1.39007

1.40102

434

Density (32) 1 of 32

Density [g·cm-3]

1.04437

Measurement Temperature [°C]

25

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 2 of 32

Density [g·cm-3]

1.03244 - 1.06278

Measurement Temperature [°C]

10 - 35

Romani; Troncoso; Carballo; Cerdeirina; Gonzalez; Journal of Chemical and Engineering Data; vol. 45; nb. 4; (2000); p. 594 - 599, View in Reaxys 3 of 32

Density [g·cm-3]

1.0478

Measurement Temperature [°C]

20

Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 4 of 32

Density [g·cm-3]

1.04625

Measurement Temperature [°C]

20

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys 5 of 32

Density [g·cm-3]

1.044

Measurement Temperature [°C]

25

Uosaki, Yasuhiro; Mutsumura, Hajime; Wakasa, Shinji; Moriyoshi, Takahashi; Journal of Chemical Thermodynamics; vol. 22; nb. 3; (1990); p. 313 - 318, View in Reaxys 6 of 32

Density [g·cm-3]

1.04465

Measurement Temperature [°C]

25

Marsh, K. N.; Rogers, H.; Journal of Chemical Thermodynamics; vol. 21; nb. 2; (1989); p. 211 - 218, View in Reaxys 7 of 32

Density [g·cm-3]

1.0377

Measurement Temperature [°C]

30

Dewan, R.K.; Sharma, A.K.; Mehta, S.K.; Journal of Solution Chemistry; vol. 17; nb. 5; (1988); p. 459 - 466, View in Reaxys 8 of 32

Density [g·cm-3]

1.03865

Measurement Temperature [°C]

30

Dewan, R. K.; Mehta, S. K.; Journal of Chemical Thermodynamics; vol. 18; nb. 2; (1986); p. 101 - 106, View in Reaxys 9 of 32

Density [g·cm-3]

1.0345

Measurement Temperature [°C]

30

Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys; Hsu; Clever; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 268,269 - 271, View in Reaxys 10 of 32

Density [g·cm-3]

1.0525

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Zhuravleva et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 46; (1976); p. 1210,1194,1195,1196,1197, View in Reaxys 11 of 32

Density [g·cm-3]

1.0422

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Reeder et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 133,134, 135, View in Reaxys 12 of 32

Density [g·cm-3]

1.05

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Tolstova et.al; J. Appl. Chem. USSR (Engl. Transl.); vol. 46; (1973); p. 907,959, View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys 13 of 32

Density [g·cm-3]

1.048

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Bahurel et al.; Bulletin de la Societe Chimique de France; (1971); p. 2331,2336, View in Reaxys 14 of 32

Density [g·cm-3]

1.052

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Matasa; Hass; Canadian Journal of Chemistry; vol. 49; (1971); p. 1284,1287, View in Reaxys 15 of 32

Density [g·cm-3]

1.0492

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Tenno; Talvik; Organic Reactivity (New York, English Translation); vol. 6; (1969); p. 315, View in Reaxys 16 of 32

Density [g·cm-3]

1.0506

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Pikhl et al.; Organic Reactivity (New York, English Translation); vol. 3; (1966); p. 297,298, View in Reaxys 17 of 32

Density [g·cm-3]

1.0139

Reference Temperature [°C]

4

Measurement Temperature [°C]

50

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 18 of 32

Density [g·cm-3]

1.0441

Reference Temperature [°C]

4

Measurement Temperature [°C]

25

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 19 of 32

Density [g·cm-3]

1.0501

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys 20 of 32

Density [g·cm-3]

1.05057

Reference Temperature [°C]

4

Measurement Temperature [°C]

20

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 21 of 32

Density [g·cm-3]

1.04464

Reference Temperature [°C]

4

Measurement Temperature [°C]

25

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 22 of 32

Density [g·cm-3]

1.0387

Reference Temperature [°C]

4

Measurement Temperature [°C]

30

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys 23 of 32

Density [g·cm-3]

1.0497 - 0.9726

Measurement Temperature [°C]

20 - 85

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys 24 of 32

Density [g·cm-3]

1.0482 - 0.9395

Measurement Temperature [°C]

18.6 - 108.5

Friend; Hargreaves; Phil.Mag.; vol. <7>34; (1943); p. 814; Chem.Abstr.; (1944); p. 1409, View in Reaxys 25 of 32

Density [g·cm-3]

1.0448

Reference Temperature [°C]

4

Measurement Temperature [°C]

25

Hunter; Partington; Journal of the Chemical Society; (1933); p. 312, View in Reaxys 26 of 32

Density [g·cm-3]

1.0528

Measurement Temperature [°C]

20

Harkins; Grafton; Journal of the American Chemical Society; vol. 42; (1920); p. 2537, View in Reaxys 27 of 32

Density [g·cm-3]

1.0472

Reference Temperature [°C]

4

Measurement Temperature [°C]

24.3

Bruehl; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 16; (1895); p. 214; Chemische Berichte; vol. 26; (1893); p. 2515, View in Reaxys 28 of 32

Density [g·cm-3]

1.0685

Reference Temperature [°C]

4

Measurement Temperature [°C]

4

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Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 29 of 32

Density [g·cm-3]

1.0561

Reference Temperature [°C]

15

Measurement Temperature [°C]

15

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 30 of 32

Density [g·cm-3]

1.0461

Reference Temperature [°C]

25

Measurement Temperature [°C]

25

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys 31 of 32

Density [g·cm-3]

0.9328

Reference Temperature [°C]

4

Measurement Temperature [°C]

114.5

Schiff,R.; Chemische Berichte; vol. 19; (1886); p. 567, View in Reaxys 32 of 32

Density [g·cm-3]

1.0582

Reference Temperature [°C]

13

Measurement Temperature [°C]

13

Meyer,V.; Justus Liebigs Annalen der Chemie; vol. 171; (1874); p. 19; Justus Liebigs Annalen der Chemie; vol. 175; (1875); p. 88, View in Reaxys Adsorption (MCS) (10) 1 of 10

Description (Adsorption (MCS))

Desorption

Comment (Adsorption (MCS))

temperature dependence

Partner (Adsorption (MCS))

Si(100)-2x1

Bocharov, Semyon; Mathauser, Anna T.; Teplyakov, Andrew V.; Journal of Physical Chemistry B; vol. 107; nb.

31; (2003); p. 7776 - 7782, View in Reaxys 2 of 10

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Temperature (Adsorption (MCS)) [°C]

-178.15 - 26.85

Partner (Adsorption (MCS))

Si(100)-2x1

Bocharov, Semyon; Mathauser, Anna T.; Teplyakov, Andrew V.; Journal of Physical Chemistry B; vol. 107; nb.

31; (2003); p. 7776 - 7782, View in Reaxys 3 of 10

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

vapour

Temperature (Adsorption (MCS)) [°C]

24

Partner (Adsorption (MCS))

peat

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Chiou; Kile; Environmental Science and Technology; vol. 28; nb. 6; (1994); p. 1139 - 1144, View in Reaxys 4 of 10

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

26.9 - 826.9

Partner (Adsorption (MCS))

clean Rh(111) surface

Hwang, S. Y.; Kong, A. C. F.; Schmidt, L. D.; Journal of Physical Chemistry; vol. 93; nb. 26; (1989); p. 8334 8343, View in Reaxys 5 of 10

Description (Adsorption (MCS))

Desorption

Temperature (Adsorption (MCS)) [°C]

26.9 - 826.9

Partner (Adsorption (MCS))

clean Pt(111) surface

Hwang, S. Y.; Kong, A. C. F.; Schmidt, L. D.; Journal of Physical Chemistry; vol. 93; nb. 26; (1989); p. 8334 8343, View in Reaxys 6 of 10

Description (Adsorption (MCS))

Chemisorption

Solvent (Adsorption (MCS))

aq. H2SO4

Partner (Adsorption (MCS))

Ru-Al Raney catalyst

Grishina, T. M.; Russian Journal of Physical Chemistry; vol. 62; nb. 11; (1988); p. 1604 - 1605; Zhurnal Fizicheskoi Khimii; vol. 62; (1988); p. 3078 - 3080, View in Reaxys 7 of 10

Description (Adsorption (MCS))

Adsorption isotherm

Solvent (Adsorption (MCS))

methanol; H2O

Partner (Adsorption (MCS))

alkylated silica gel

Guglya, E. B.; Yanovskii, S. M.; Russian Journal of Physical Chemistry; vol. 60; nb. 12; (1986); p. 1846 - 1849; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 3069 - 3073, View in Reaxys 8 of 10

Description (Adsorption (MCS))

Further physical properties of the adsorbed molecule

Partner (Adsorption (MCS))

platinum electrode

Grishina, T. M.; Meshcheryakova, E. V.; Russian Journal of Physical Chemistry; vol. 59; nb. 10; (1985); p. 1450 1453; Zhurnal Fizicheskoi Khimii; vol. 59; nb. 10; (1985); p. 2436 - 2439, View in Reaxys 9 of 10

Description (Adsorption (MCS))

Adsorption

Solvent (Adsorption (MCS))

aq. H2SO4

Partner (Adsorption (MCS))

Raney catlysts

Nesterenko, L.N.; Grishina, T. M.; Russian Journal of Physical Chemistry; vol. 56; nb. 1; (1982); p. 44 - 46; Zhurnal Fizicheskoi Khimii; vol. 56; nb. 1; (1982); p. 76 - 79, View in Reaxys 10 of 10

Description (Adsorption (MCS))

Adsorption

Grishina; Vovchenko; Russian Journal of Physical Chemistry; vol. 53; (1979); p. 1523; ; p. 2660, View in Reaxys; Kolganova et al.; Russian Journal of Physical Chemistry; vol. 50; (1976); p. 624, View in Reaxys Association (MCS) (19)

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1 of 19

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

25

Comment (Association (MCS))

film

Partner (Association (MCS))

cycloheptaamylose

Shtykov; Korenman; Rusanova; Gorin; Kalach; Pankin; Doklady Chemistry; vol. 396; nb. 4-6; (2004); p. 119 121, View in Reaxys 2 of 19

Description (Association Association with compound (MCS)) Partner (Association (MCS))

2,2'-bis(2,7-di-tert-butyl-9-hydroxyfluoren-9-yl)biphenyl

Weber; Wierig; Skobridis; Advanced Synthesis and Catalysis; vol. 338; nb. 6; (1996); p. 553 - 557, View in Reaxys 3 of 19

Description (Association Association with compound (MCS)) Partner (Association (MCS))

9,9'-lt;2,2'-(1,1'-biphenyl)ylenegt;bis(9H-fluoren-9-ol)

Weber; Wierig; Skobridis; Advanced Synthesis and Catalysis; vol. 338; nb. 6; (1996); p. 553 - 557, View in Reaxys 4 of 19

Description (Association NMR spectrum of the complex (MCS)) Partner (Association (MCS))

PMDBD

Boyle, Peter H.; Convery, Maire A.; Davis, Anthony P.; Hosken, Gladys D.; Murray, Brian A.; Journal of the Chemical Society, Chemical Communications; nb. 3; (1992); p. 239 - 242, View in Reaxys 5 of 19

Description (Association NMR spectrum of the complex (MCS)) Solvent (Association (MCS))

benzene-d6

Partner (Association (MCS))

PMDBD

Boyle, Peter H.; Convery, Maire A.; Davis, Anthony P.; Hosken, Gladys D.; Murray, Brian A.; Journal of the Chemical Society, Chemical Communications; nb. 3; (1992); p. 239 - 242, View in Reaxys 6 of 19

Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

cetane

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 7 of 19

Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

cholic acid

Miyata, Mikiji; Shibakami, Motonari; Goonewardena, Wyjayanthi; Takemoto, Kiichi; Chemistry Letters; (1987); p. 605 - 608, View in Reaxys 8 of 19

Description (Association Association with compound (MCS)) Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

water

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Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Carr, Peter W.; Doherty, Robert F.; Taft, Robert W.; Journal of Physical Chemistry; vol. 91; nb. 7; (1987); p. 1996 - 2004, View in Reaxys 9 of 19

Description (Association NMR spectrum of the complex (MCS)) Temperature (Association (MCS)) [°C]

-70

Partner (Association (MCS))

4,7,13,16,21-pentaoxa-1,10-diazabicyclo-[8,8,5-tricosane

Schmidt, Emmanuel; Tremillon, Jean-Michel; Kintzinger, Jean-Pierre; Popov, Alexander I.; Journal of the American Chemical Society; vol. 105; nb. 26; (1983); p. 7563 - 7566, View in Reaxys 10 of 19

Description (Association Further physical properties of the complex (MCS)) Partner (Association (MCS))

cyclohexane

Sanchez, G.; Garland, C. W.; Journal of Chemical Physics; vol. 79; nb. 6; (1983); p. 3100 - 3103, View in Reaxys 11 of 19

Description (Association Association with compound (MCS)) Solvent (Association (MCS))

methylcyclohexane

Temperature (Association (MCS)) [°C]

0 - 90

Partner (Association (MCS))

tris(dimethylamino)phosphine oxide

Fujiwara, Hideaki; Takagi, Tatsuya; Yamazaki, Yutaka; Sasaki, Yoshio; Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases; vol. 78; (1982); p. 347 - 356, View in Reaxys 12 of 19

Description (Association Dipole moment of the complex (MCS)) Solvent (Association (MCS))

benzene

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

AlBr3

Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 13 of 19

Description (Association Enthalpy of association (MCS)) Solvent (Association (MCS))

benzene

Temperature (Association (MCS)) [°C]

25

Partner (Association (MCS))

AlBr3

Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 14 of 19

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

benzene

Partner (Association (MCS))

AlBr3

Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys

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15 of 19

Description (Association IR spectrum of the complex (MCS)) Solvent (Association (MCS))

benzene

Partner (Association (MCS))

GaBr3

Gur'yanova, E. N.; Isaeva, E. S.; Shifrina, R. R.; Lechkina, L. I.; Kharlamova, E. N.; Terent'ev, V. A.; J. Gen. Chem. USSR (Engl. Transl.); vol. 50; nb. 3; (1980); p. 667 - 673,547 - 552, View in Reaxys 16 of 19

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

dodecane

Partner (Association (MCS))

29H,31H-Phthalocyanine; polymethyl methacrylate

Ahuja, R. C.; Hauffe, K.; Berichte der Bunsen-Gesellschaft; vol. 84; nb. 2; (1980); p. 129 - 137, View in Reaxys 17 of 19

Description (Association Further physical properties of the complex (MCS)) Solvent (Association (MCS))

dodecane

Partner (Association (MCS))

vat yellow 1; polymethyl methacrylate

Ahuja, R. C.; Hauffe, K.; Berichte der Bunsen-Gesellschaft; vol. 84; nb. 5; (1980); p. 487 - 494, View in Reaxys 18 of 19

Description (Association Association with compound (MCS)) Gordon; Thorne; Journal of Physical Chemistry; vol. 73; (1969); p. 3643,3648, View in Reaxys; Karshibaev; Beridze; Moscow University Chemistry Bulletin (English Translation); vol. 27; nb. 1; (1971); p. 65; ; p. 92, View in Reaxys

19 of 19

Description (Association Spectrum of the complex (MCS)) Baitinger et al.; Tetrahedron; vol. 20; (1964); p. 1635,1639, View in Reaxys; Su; Hong; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1461,1464, View in Reaxys

Azeotropes (MCS) (30) 1 of 30

Malesinska; Malesinski; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 8; (1960); p. 191,193, View in Reaxys

2 of 30

Temperature (Azeotropes (MCS)) [°C]

87.1

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

water

Ericsson; Industrial and Engineering Chemistry; vol. 35; (1943); p. 1028, View in Reaxys 3 of 30

Temperature (Azeotropes (MCS)) [°C]

96

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl bromide

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.292, View in Reaxys 4 of 30

Temperature (Azeotropes (MCS)) [°C]

61.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methanol

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Marsden,C.; Solvents Manual <London 1954>S.236, View in Reaxys 5 of 30

Temperature (Azeotropes (MCS)) [°C]

89.2

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

heptane

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.311, View in Reaxys 6 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

toluene

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.311, View in Reaxys 7 of 30

Temperature (Azeotropes (MCS)) [°C]

112.4

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

acetic acid

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.23, View in Reaxys 8 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propyl nitrate

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.256, View in Reaxys 9 of 30

Temperature (Azeotropes (MCS)) [°C]

107.7

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyl alcohol

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.103, View in Reaxys 10 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

n-amyl alcohol

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.103, View in Reaxys 11 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

propyl alcohol

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.103, View in Reaxys 12 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isopentyl bromide

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.292, View in Reaxys 13 of 30

Temperature (Azeotropes (MCS)) [°C]

112.5

Pressure (Azeotropes (MCS)) [Torr]

760

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Azeotropes

isobutyl acetate

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.256, View in Reaxys 14 of 30

Temperature (Azeotropes (MCS)) [°C]

112

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isoamyl alcohol

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.103, View in Reaxys 15 of 30

Temperature (Azeotropes (MCS)) [°C]

89.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl bromide

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.292, View in Reaxys 16 of 30

Temperature (Azeotropes (MCS)) [°C]

102.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyl alcohol

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.103, View in Reaxys 17 of 30

Temperature (Azeotropes (MCS)) [°C]

90.8

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylcyclohexane

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.311, View in Reaxys 18 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

#tert!-amyl alcohol

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.103, View in Reaxys 19 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

diisopropyl sulfide

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.330, View in Reaxys 20 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

methylcyclopentane

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.311, View in Reaxys 21 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

2.5-dimethyl-hexane

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.311, View in Reaxys

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22 of 30

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

butyric acid ethyl ester

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.256, View in Reaxys 23 of 30

Temperature (Azeotropes (MCS)) [°C]

108.5

Pressure (Azeotropes (MCS)) [Torr]

760

Azeotropes

isobutyric acid ethyl ester

Horsley,L.H.; Azeotropic Data (= Advances in Chemistry Series Nr.6) <Washington 1952>S.271, View in Reaxys; Lecat,M.; Tables azeotropiques, 2.Aufl. <Bruessel 1949>S.256, View in Reaxys 24 of 30

Azeotropes

#tert!-butyl alcohol

Horsley; Azeotropic Data II <=Advances in Chemistry Series Nr. 35)<Washington 1962>S.76, View in Reaxys 25 of 30

Azeotropes

butan-1-ol

Horsley; Azeotropic Data II <=Advances in Chemistry Series Nr. 35)<Washington 1962>S.76, View in Reaxys 26 of 30

Azeotropes

ethanol

Horsley; Azeotropic Data II <=Advances in Chemistry Series Nr. 35)<Washington 1962>S.76, View in Reaxys 27 of 30

Azeotropes

isobutyl alcohol

Horsley; Azeotropic Data II <=Advances in Chemistry Series Nr. 35)<Washington 1962>S.76, View in Reaxys 28 of 30

Azeotropes

propan-1-ol

Horsley; Azeotropic Data II <=Advances in Chemistry Series Nr. 35)<Washington 1962>S.76, View in Reaxys 29 of 30

Azeotropes

propan-2-ol

Horsley; Azeotropic Data II <=Advances in Chemistry Series Nr. 35)<Washington 1962>S.76, View in Reaxys 30 of 30

Azeotropes

water

Horsley; Azeotropic Data II <=Advances in Chemistry Series Nr. 35)<Washington 1962>S.76, View in Reaxys Boundary Surface Phenomena (MCS) (3) 1 of 3

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Partner (Boundary Surface Phenomena (MCS))

2-Methylpentane

McLure, Ian A.; Pegg, Ian L.; Journal of Molecular Structure; vol. 80; (1982); p. 393 - 400, View in Reaxys 2 of 3

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Wims et al.; Journal of Physical Chemistry; vol. 74; (1970); p. 3042, View in Reaxys 3 of 3

Description (Boundary Surface Phenomena (MCS))

Interfacial tension

Comment (Boundary Surface Phenomena (MCS))

zwischen Quecksilber und Nitroaethan bei 20grad.

Harkins; Grafton; Journal of the American Chemical Society; vol. 42; (1920); p. 2537, View in Reaxys Chromatographic Data (1) Chromatographic Location data

References

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HPLC (High performance liquid chromatography)

supporting information

Sureshkumar, Devarajulu; Hashimoto, Kazuki; Kumagai, Naoya; Shibasaki, Masakatsu; Journal of Organic Chemistry; vol. 78; nb. 22; (2013); p. 11494 - 11500, View in Reaxys

Circular Dichroism (1) References Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p.

907,908, View in Reaxys Compressibility (1) Description (Com- References pressibility) Isothermal compressibility

Uosaki, Yasuhiro; Mutsumura, Hajime; Wakasa, Shinji; Moriyoshi, Takahashi; Journal of Chemical Thermodynamics; vol. 22; nb. 3; (1990); p. 313 - 318, View in Reaxys

Conformation (1) Object of Investi- References gation Conformation

Stone; Maki; Journal of Chemical Physics; vol. 37; (1962); p. 1326,1329, View in Reaxys; Shakhparonov et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 1425; ; p. 2543, View in Reaxys; ChapeletLetourneux et al.; Bulletin de la Societe Chimique de France; (1968); p. 3963, View in Reaxys; Beresneva, G. A.; Khristenko, L. V.; Ul'yanova, O. D.; Pentin, Yu. A.; Russian Journal of Physical Chemistry; vol. 60; nb. 4; (1986); p. 631 - 632; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 1045 - 1046, View in Reaxys

Critical Temperature (1) Critical Tempera- References ture [°C] 21.25

Baranowska-Majgier, Helena; Pyzuk, Wieslaw; Jeute, Wojciech; Ziolo, Jerzy; Journal of Chemical & Engineering Data; vol. 26; nb. 1; (1981); p. 51 - 53, View in Reaxys

Crystal Phase (1) Description (Crys- References tal Phase) Solid state structure properties

Weiss; Weiss; Angewandte Chemie; vol. 72; (1960); p. 413, View in Reaxys

Dielectric Constant (5) Dielectric ConFrequency (Diestant lectric Constant) [Hz]

Temperature (Die- References lectric Constant) [°C]

28.06

28.96

Kocsis, Laura S.; Kagalwala, Husain N.; Mutto, Sharlene; Godugu, Bhaskar; Bernhard, Stefan; Tantillo, Dean J.; Brummond, Kay M.; Journal of Organic Chemistry; vol. 80; nb. 23; (2015); p.

11686 - 11698, View in Reaxys 2E+06

20

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 Oelschlaeger,H. et al.; Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft; vol. 296; (1963); p. 107 120, View in Reaxys; Schlundt; Chem. Zentralbl.; vol. 73; nb. I; (1902); p. 3, View in Reaxys; Barnard et al.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1976); p. 961,964, View in Reaxys; Zboinski et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol.

27; (1979); p. 85,87,91, View in Reaxys; Mayahi; Hussain; Journal of the Indian Chemical Society; vol. 50; (1973); p. 34, View in Reaxys; Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys; Ovsoyan; Levina; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1531; ; p. 2672, View in Reaxys; Honda; Sasada; Japanese Journal of Applied Physics; vol. 16; (1977); p.

1775,1776-1778, View in Reaxys

30.6

18

Cowley; Partington; Journal of the Chemical Society; (1933); p.

1252, View in Reaxys

1.03

99.9

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

Dissociation Energy (1)

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References Cumming et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 3474,3477, View in Reaxys Dissociation Exponent (27) 1 of 27

Dissociation Exponent (pK)

10.1

Solvent (Dissociation Exponent)

acetonitrile

Method (Dissociation Exponent)

conductometric

Type (Dissociation Exponent)

a1/apparent

Comment (Dissociation Exponent)

ambient temperature

Nag, Samik; Datta, Dipankar; Indian Journal of Chemistry - Section A Inorganic, Physical, Theoretical and Analytical Chemistry; vol. 46; nb. 8; (2007); p. 1263 - 1265, View in Reaxys 2 of 27

Type (Dissociation Exponent)

a1/apparent

Bordwell, Frederick G.; Satish; Journal of the American Chemical Society; vol. 116; nb. 20; (1994); p. 8885 - 8889, View in Reaxys 3 of 27

Dissociation Exponent (pK)

8.31 - 8.44

Dissociation Group

CH2-NO2

Temperature (Dissociation Exponent) [°C]

25 - 45

Solvent (Dissociation Exponent)

H2O

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Bunting, John W.; Stefanidis, Dimitrios; Canadian Journal of Chemistry; vol. 67; (1989); p. 428 - 432, View in Reaxys 4 of 27

Dissociation Exponent (pK)

8.6

Dissociation Group

C-H

Temperature (Dissociation Exponent) [°C]

25

Solvent (Dissociation Exponent)

H2O; various solvent(s)

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

a1/apparent

Gilbert, H. F.; Journal of the American Chemical Society; vol. 102; nb. 23; (1980); p. 7059 - 7065, View in Reaxys 5 of 27

Comment (Dissociation Exponent)

(pk')pKa

Bradamante; Pagani; Journal of Organic Chemistry; vol. 44; (1979); p. 4737,4738, View in Reaxys 6 of 27

Comment (Dissociation Exponent)

(pk')pK(a)

Yur'ev et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 48; (1978); p. 149,128, View in Reaxys 7 of 27

Comment (Dissociation Exponent)

(k')K

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Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3107,3108, View in Reaxys 8 of 27

Comment (Dissociation Exponent)

(pk')pK

Bordwell,F.G.; Bartmess,J.E.; Journal of Organic Chemistry; vol. 43; (1978); p. 3101 - 3107, View in Reaxys; Cumming et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 3474,3477, View in Reaxys; Bordwell et al.; Journal of Organic Chemistry; vol. 43; (1978); p. 3095,3096, View in Reaxys; Lipina; Perekalin; Acta Physica et Chemica; vol. 19; (1973); p. 125,129, View in Reaxys 9 of 27

Comment (Dissociation Exponent)

(pk')pK(a)-Werte in versch. Lsgsm. (Tab.1)

Cox; Gibson; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1977); p. 1812,1813, 1814, View in Reaxys 10 of 27

Comment (Dissociation Exponent)

(pk')pK: 16.7

Bordwell et al.; Journal of Organic Chemistry; vol. 42; (1977); p. 326,331, View in Reaxys 11 of 27

Comment (Dissociation Exponent)

(pk')pKa (Tab.I)

Spinner; Journal of Organic Chemistry; vol. 40; (1975); p. 3580,3581,3583, View in Reaxys 12 of 27

Comment (Dissociation Exponent)

(pk')der pK(S)-Wert bei Ritchie,Uschold,J.Am.Chem.Soc.90<1968>2821 ist um 2.1 zu niedrig angegeben

Matthews et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7006,7007-7014, View in Reaxys 13 of 27

Comment (Dissociation Exponent)

(pk)absoluter pK(S)-Wert in DMSO

Matthews et al.; Journal of the American Chemical Society; vol. 97; (1975); p. 7006,7007-7014, View in Reaxys 14 of 27

Comment (Dissociation Exponent)

(pk')pK des Acetat-kat. Proton-Transfers in (CH3)2SO-H2O

Cox; Gibson; Journal of the Chemical Society, Chemical Communications; (1974); p. 638, View in Reaxys 15 of 27

Comment (Dissociation Exponent)

(pk')in waessriger Lsg.

Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys 16 of 27

Comment (Dissociation Exponent)

(pk')pK (Acn.)

Fedorov; Aksenenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1166; ; p. 2040, View in Reaxys 17 of 27

Comment (Dissociation Exponent)

(pk')pK (Tributylphosphate)

Fedorov; Aksenenko; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1166; ; p. 2040, View in Reaxys 18 of 27

Comment (Dissociation Exponent)

(k')Tabelle 6

Belikov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 272,275; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 335, View in Reaxys 19 of 27

Comment (Dissociation Exponent)

(pk')pK(a) in DMSO

Faleev et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1970); p. 69; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1970); p. 73, View in Reaxys 20 of 27

Comment (Dissociation Exponent)

(pk')pK (DMF)

Fedorov et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 838; Zhurnal Fizicheskoi Khimii; vol. 43; (1969); p. 1508, View in Reaxys 21 of 27

Comment (Dissociation Exponent)

(pk')pK(a): 14.31

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Belonkon' et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1969); p. 949,950,954; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1969); p. 1039, View in Reaxys 22 of 27

Comment (Dissociation Exponent)

(pk')pK-Wert

Ritchie,C.D.; Uschold,R.E.; Journal of the American Chemical Society; vol. 90; nb. 11; (1968); p. 2821 - 2824, View in Reaxys 23 of 27

Comment (Dissociation Exponent)

(pk')in Wasser (Temp. nicht angegeben, spektrophotom. ermittelt)

Nowikow et al.; Tetrahedron, Supplement; vol. 6; (1964); p. 119,128; Chem.Abstr.; nb. 14665; (1965), View in Reaxys 24 of 27

Dissociation Exponent (pK)

8.49

Temperature (Dissociation Exponent) [°C]

18

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Turnbull; Maron; Journal of the American Chemical Society; vol. 65; (1943); p. 214,215, View in Reaxys 25 of 27

Dissociation Exponent (pK)

8.46

Temperature (Dissociation Exponent) [°C]

25

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Turnbull; Maron; Journal of the American Chemical Society; vol. 65; (1943); p. 214,215, View in Reaxys 26 of 27

Dissociation Exponent (pK)

8.44

Temperature (Dissociation Exponent) [°C]

30

Method (Dissociation Exponent)

potentiometric

Type (Dissociation Exponent)

apparent

Turnbull; Maron; Journal of the American Chemical Society; vol. 65; (1943); p. 214,215, View in Reaxys 27 of 27

Type (Dissociation Exponent)

apparent

Maron; Shedlovsky; Journal of the American Chemical Society; vol. 61; (1939); p. 754, View in Reaxys; Junell; Arkiv foer Kemi; vol. 11; p. B Nr.30,S.6; Chem. Zentralbl.; vol. 105; nb. I; (1934); p. 3727, View in Reaxys Dynamic Viscosity (4) Dynamic Viscosi- Temperature (Dyty [P] namic Viscosity) [°C]

References

0.00638

25

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys

0.0068

20

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb. 4; (1988); p. 402 - 404, View in Reaxys

0.00661

25

Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys

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0.003162 0.007704

18.6 - 108.5

Friend; Hargreaves; Phil.Mag.; vol. <7>34; (1943); p. 814; Chem.Abstr.; (1944); p.

1409, View in Reaxys

Electrical Data (6) 1 of 6

Description (Electrical Data)

Electrical properties

Location

supporting information

Prakash, G. K. Surya; Wang, Fang; Ni, Chuanfa; Shen, Jingguo; Haiges, Ralf; Yudin, Andrei K.; Mathew, Thomas; Olah, George A.; Journal of the American Chemical Society; vol. 133; nb. 26; (2011); p. 9992 - 9995, View in Reaxys 2 of 6

Description (Electrical Data)

Dielectric anisotropy

Zboinski et al.; Chemical Physics; vol. 40; (1979); p. 77,83, View in Reaxys 3 of 6

Description (Electrical Data)

Electrical conductivity

Little; Singleterry; Journal of Physical Chemistry; vol. 68; (1964); p. 2709, View in Reaxys; Mayahi; Hussain; Journal of the Indian Chemical Society; vol. 50; (1973); p. 34, View in Reaxys 4 of 6

Description (Electrical Data)

Dielectric loss

Ovsoyan; Levina; Russian Journal of Physical Chemistry; vol. 46; (1972); p. 1531; ; p. 2672, View in Reaxys 5 of 6

Description (Electrical Data)

Dielectric relaxation time

Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys 6 of 6

Description (Electrical Data)

Electrical properties

Krishnamurthy,V.N.; Soundararajan,S.; Indian Journal of Chemistry; vol. 3; (1965); p. 479 - 481, View in Reaxys Electrical Moment (16) 1 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

2.94

Borovikov; Makovetskii; Pivovarova; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol.

100; nb. 1; (1996); p. 33 - 38, View in Reaxys 2 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.47

Temperature (Electrical Moment) [°C]

30

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

cyclohexane

Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 3 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.54

Temperature (Electrical Moment) [°C]

30

Method (Electrical Moment)

Dielectric constant (ε)

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Solvent (Electrical Moment)

1,3,5-trimethyl-benzene

Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 4 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.56

Temperature (Electrical Moment) [°C]

30

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

xylene

Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 5 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.59

Temperature (Electrical Moment) [°C]

30

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

benzene

Yadava, R. R.; Singh, V. N.; Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical; vol. 21; nb. 1; (1982); p. 17 - 19, View in Reaxys 6 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.7

Temperature (Electrical Moment) [°C]

19.9

Solvent (Electrical Moment)

benzene

Balakier, Grazyna; Polish Journal of Chemistry; vol. 54; nb. 11/12; (1980); p. 2297 - 2304, View in Reaxys 7 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.7

Temperature (Electrical Moment) [°C]

19.9

Solvent (Electrical Moment)

CCl4

Balakier, Grazyna; Polish Journal of Chemistry; vol. 54; nb. 11/12; (1980); p. 2297 - 2304, View in Reaxys 8 of 16

Description (Electrical Moment)

Dipole moment

Nelson et al.; Journal of Physical Chemistry; vol. 71; (1967); p. 2742, View in Reaxys; Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p.

379, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys; Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys

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9 of 16

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

μ

Zboinski et al.; Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques; vol. 27; (1979); p.

85,87,91, View in Reaxys; Bahurel et al.; Bulletin de la Societe Chimique de France; (1971); p. 2331,2336, View in Reaxys; Polezzo; Simonetta; Chemical Physics Letters; vol. 1; (1967); p. 85, View in Reaxys; Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys 10 of 16

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

Table 1

Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys 11 of 16

Description (Electrical Moment)

Dipole moment

Comment (Electrical Moment)

3,2 D

Oelschlaeger,H. et al.; Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft; vol.

296; (1963); p. 107 - 120, View in Reaxys; Luzkii; Obuchowa; J. Gen. Chem. USSR (Engl. Transl.); vol. 31; (1961); p. 2692,2512; Chem.Abstr.; vol. 57; nb. 64; (1962), View in Reaxys 12 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.54

Method (Electrical Moment)

Dielectric constant (ε)

Solvent (Electrical Moment)

neat (no solvent)

Osipow; Zhurnal Fizicheskoi Khimii; 31<1957<1542,1544; Chem.Abstr.; (1958); p. 5911, View in Reaxys 13 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.7

Method (Electrical Moment)

Dielectric constant (ε)

Comment (Electrical Moment)

Dipolmoment::Dampf.

Hurdis; Smyth; Journal of the American Chemical Society; vol. 64; (1942); p. 2832, View in Reaxys 14 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.58

Method (Electrical Moment)

Dielectric constant (ε)

Comment (Electrical Moment)

Dipolmoment::Dampf.

Groves; Sugden; Journal of the Chemical Society; (1937); p. 162, View in Reaxys 15 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

3.19

Method (Electrical Moment)

Dielectric constant (ε)

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Solvent (Electrical Moment)

benzene

Hunter; Partington; Journal of the Chemical Society; (1933); p. 312, View in Reaxys 16 of 16

Description (Electrical Moment)

Dipole moment

Moment (Electrical Moment) [D]

4.03

Comment (Electrical Moment)

Dipolmoment::Dampf.

Hoejendahl; Phys.Z.; vol. 30; (1929); p. 392, View in Reaxys Electrochemical Behaviour (9) Description (Elec- Comment (Electrochemical Betrochemical Behaviour) haviour)

References

Electrolytic dissociation / protonation equilibrium

Yano, Yumihiko; Ohshima, Masashi; Sutoh, Susumu; Journal of the Chemical Society, Chemical Communications; nb. 11; (1984); p. 695 - 696, View in Reaxys; Bordwell, Frederick G.; Satish; Journal of the American Chemical Society; vol. 116; nb. 20; (1994); p. 8885 - 8889, View in Reaxys

Proton affinity

Zhu, Zhiqing; Gaeumann, Tino; Organic Mass Spectrometry; vol. 28; nb. 10; (1993); p.

1111 - 1118, View in Reaxys

Kinetics of dissociation (electrolytic) / protonation

Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys; Gold, Victor; Laali, Khosrow; Morris, Kenneth P.; Zdunek, Leszek Z.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1985); p. 865 - 870, View in Reaxys

Thermodynamic parameters for dissociation / protonation

Arnett, Edward M.; Venkatasubramaniam, K. G.; Journal of Organic Chemistry; vol.

48; nb. 10; (1983); p. 1569 - 1578, View in Reaxys; Gold, Victor; Laali, Khosrow; Morris, Kenneth P.; Zdunek, Leszek Z.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1985); p. 865 - 870, View in Reaxys

Acidity

Cumming; Kebarle; Canadian Journal of Chemistry; vol. 56; (1978); p. 1,5, View in Reaxys; Cumming; Kebarle; Journal of the American Chemical Society; vol.

100; (1978); p. 1835,1836, View in Reaxys

Electrochemical properties

Glushchenko; Radaev; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 27; (1978); p. 463; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 27; (1978); p. 538, View in Reaxys

Polarography

Gupta; Raghavan; Indian Journal of Chemistry; vol. 9; (1971); p. 233, View in Reaxys; Tur'jan; Tmekalowa; J. Appl. Chem. USSR (Engl. Transl.); vol. 35; (1962); p.

2729,2618; Chem.Abstr.; vol. 59; nb. 2605; (1963), View in Reaxys; Paramonov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 26; (1977); p. 509,510-511,513; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 26; (1977); p. 567, View in Reaxys; Gavioli et al.; Collection of Czechoslovak Chemical Communications; vol. 36; (1971); p. 730,733, 736, View in Reaxys

Enthalpy of disso- . ciation (electrolytic) / protonation

Matsui; Hepler; Canadian Journal of Chemistry; vol. 51; (1973); p. 1941,1943, View in Reaxys

pH of aqueous solutions

einer 0.01 m-Loe- Ericsson; Industrial and Engineering Chemistry; vol. 35; (1943); p. 1028, View in Reaxys sung bei 25grad: 6.0.

Electrochemical Characteristics (15) 1 of 15

Description (Electrochemical Characteristics)

voltammetry

Solvent (Electrochemical Characteristics)

neat liquid

Temperature (Electrochemical Characteristics) [°C]

21

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Caban, Karolina; Donten, Mikolaj; Stojek, Zbigniew; Journal of Physical Chemistry B; vol. 108; nb. 3; (2004); p.

1153 - 1159, View in Reaxys 2 of 15

Description (Electrochemical Characteristics)

polarographic half-wave potential

Solvent (Electrochemical Characteristics)

acetonitrile

Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.97 V; Product: /BRN= 6965001/. No. of transm. electrons: 1. Method: polarography. Deical Characteristics) scription: vs. Ag/0.1M AgClO4-MeCN; effects of tetraalkylammonium and alkali metal ions Product

C2H6NO2(1-)

Hojo, Masashi; Nishikawa, Kazukiyo; Akita, Yoshihiro; Imai, Yoshihiko; Bulletin of the Chemical Society of Japan; vol. 59; nb. 12; (1986); p. 3815 - 3820, View in Reaxys 3 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 1.09 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -0.96 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 4 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 2.1 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.01 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 5 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 3.12 cal Characteristics)

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Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.08 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 6 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 4.05 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.13 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 7 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 5.08 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.18 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 8 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 6.11 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.2 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys

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9 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 7.12 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.21 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 10 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 8.15 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.22 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 11 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 9.1 cal Characteristics) Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.22 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 12 of 15

Description (Electrochemical Characteristics)

redox potential

Solvent (Electrochemical Characteristics)

acetonitrile; methanol

pH-Value (Electrochemi- 10.05 cal Characteristics)

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35/129

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Temperature (Electrochemical Characteristics) [°C]

25

Comment (Electrochem- -1.22 V; Product: /BRN= 773646/. No. of transm. electrons: 4. Method: cyclovoltammetry ical Characteristics) Product

N-hydroxy-N-ethylamine

Theodoridou, E.; Jannakoudakis, A.D.; Jannakoudakis, D.; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 134; (1983); p. 227 - 242, View in Reaxys 13 of 15

Description (Electrochemical Characteristics)

polarographic half-wave potential

Kargin et al.; J. Gen. Chem. USSR (Engl. Transl.); vol. 47; (1977); p. 166,153,155,156, View in Reaxys; Bauer; Wendt; Journal of Electroanalytical Chemistry and Interfacial Electrochemistry; vol. 80; (1977); p. 395, View in Reaxys; Gavioli et al.; Collection of Czechoslovak Chemical Communications; vol. 36; (1971); p. 730,733, 736, View in Reaxys 14 of 15

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Petru; Collection of Czechoslovak Chemical Communications; vol. 12; (1947); p. 621; Chem.Abstr.; (1948); p. 5354, View in Reaxys; de Vries; Ivett; Industrial and Engineering Chemistry, Analytical Edition; vol. 13; (1941); p. 339, View in Reaxys; Miller; Arnold; Astle; Journal of the American Chemical Society; vol. 70; (1948); p. 3974, View in Reaxys; Stewart; Bonner; Analytical Chemistry; vol. 22; (1950); p. 793, View in Reaxys; Radin; De Vries; Analytical Chemistry; vol. 24; (1952); p. 971, View in Reaxys; Bergman; James; Transactions of the Faraday Society; vol. 48; (1952); p. 956,960; Transactions of the Faraday Society; vol. 50; (1954); p. 60,63, View in Reaxys 15 of 15

Description (Electrochemical Characteristics)

polarographic current/voltage curve

Comment (Electrochem- polarographische Ermittlung der Umwandlungsgeschwindigkeit. ical Characteristics) Miller; Arnold; Astle; Journal of the American Chemical Society; vol. 70; (1948); p. 3974, View in Reaxys Electron Binding (1) Description (Elec- References tron Binding) Electron affinity

Cumming et al.; Canadian Journal of Chemistry; vol. 55; (1977); p. 3474,3477, View in Reaxys

Energy Data (MCS) (27) 1 of 27

Description (Energy Data (MCS))

Molar excess Gibbs free energy

Temperature (Energy Data (MCS)) [°C]

25

Pressure (Energy Data (MCS)) [Torr]

760

Comment (Energy Data (MCS))

gas

Partner (Energy Data (MCS))

cetane

Jamalizadeh; Hosseini; Russian Journal of Physical Chemistry A; vol. 80; nb. 9; (2006); p. 1423 - 1427, View in Reaxys 2 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

35

Partner (Energy Data (MCS))

hexane

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys

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3 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

45

Partner (Energy Data (MCS))

octanol

Feng, Hui; Wang, Yanru; Shi, Jun; Benson, George C.; Lu, Benjamin C.-Y.; Journal of Chemical Thermodynamics; vol. 23; nb. 2; (1991); p. 169 - 174, View in Reaxys 4 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

cyclohexane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 5 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

methanol

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 6 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

diethyl ether

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 7 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

dichloromethane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 8 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

acetonitrile

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 9 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

H2O

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys

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10 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

nitromethane

Trampe; Eckert; Journal of Chemical and Engineering Data; vol. 36; nb. 1; (1991); p. 112 - 118, View in Reaxys 11 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

20 - 40

Pressure (Energy Data (MCS)) [Torr]

759.8

Partner (Energy Data (MCS))

2,2,4-trimethylpentane

Battler, John R.; Rowley, Richard L.; Journal of Chemical & Engineering Data; vol. 35; nb. 3; (1990); p. 334 - 338, View in Reaxys 12 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Partner (Energy Data (MCS))

2,2,4-trimethylpentane

Battler, John R.; Rowley, Richard L.; Journal of Chemical & Engineering Data; vol. 35; nb. 3; (1990); p. 334 - 338, View in Reaxys 13 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

23 - 25

Partner (Energy Data (MCS))

cyclohexane

Marsh, K. N.; Rogers, H.; Journal of Chemical Thermodynamics; vol. 21; nb. 2; (1989); p. 211 - 218, View in Reaxys 14 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Partner (Energy Data (MCS))

cyclohexane

Johnson, K. A.; Journal of Chemical Thermodynamics; vol. 20; nb. 7; (1988); p. 889 - 896, View in Reaxys 15 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 45

Partner (Energy Data (MCS))

cyclohexane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 16 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25 - 45

Partner (Energy Data (MCS))

tetrachloromethane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 17 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

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Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

para-xylene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 18 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

benzene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 19 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

hexane

Costas, Miguel; Patterson, Donald; Journal of Solution Chemistry; vol. 11; (1982); p. 807 - 822, View in Reaxys 20 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

2-Methylpentane

Costas, Miguel; Patterson, Donald; Journal of Solution Chemistry; vol. 11; (1982); p. 807 - 822, View in Reaxys 21 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

3-methyl-pentane

Costas, Miguel; Patterson, Donald; Journal of Solution Chemistry; vol. 11; (1982); p. 807 - 822, View in Reaxys 22 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

2,3-dimethyl-butane

Costas, Miguel; Patterson, Donald; Journal of Solution Chemistry; vol. 11; (1982); p. 807 - 822, View in Reaxys 23 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Temperature (Energy Data (MCS)) [°C]

25

Partner (Energy Data (MCS))

neohexane

Costas, Miguel; Patterson, Donald; Journal of Solution Chemistry; vol. 11; (1982); p. 807 - 822, View in Reaxys 24 of 27

Description (Energy Data (MCS))

Excess thermochemical parameter

Orye; Prausnitz; Transactions of the Faraday Society; vol. 61; (1965); p. 1338,1340, View in Reaxys; Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys; Clever; Hsu; Journal of Chemical Thermodynamics; vol. 10; (1978); p. 213,214, 216 - 218, View in Reaxys; Handa et al.; Journal of Chemi-

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cal Thermodynamics; vol. 9; (1977); p. 451,459, View in Reaxys; Hsu; Clever; Journal of Chemical and Engineering Data; vol. 20; (1975); p. 268,269 - 271, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys; Nicolaides; Eckert; Journal of Chemical and Engineering Data; vol. 23; (1978); p.

152,154, View in Reaxys 25 of 27

Description (Energy Data (MCS))

Thermodynamic properties of system with

Snyder; Eckert; Journal of Chemical and Engineering Data; vol. 18; (1973); p. 282,283-285, View in Reaxys 26 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Orye; Prausnitz; Transactions of the Faraday Society; vol. 61; (1965); p. 1338,1340, View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys; Anderson et al.; AIChE Journal; vol. 8; (1962); p. 66,67, View in Reaxys 27 of 27

Description (Energy Data (MCS))

Enthalpy of mixing

Partner (Energy Data (MCS))

Glutaronitrile

Phibbs; Journal of Physical Chemistry; vol. 59; (1955); p. 346,249, View in Reaxys Enthalpies of Other Phase Transitions (1) Enthalpies of Oth- Comment (EnReferences er Phase Transi- thalpies of Other tions [Jmol-1] Phase Transitions) -8620

From transfer Goffredi, Mario; Liszi, Janos; Nemeth, Bela; Liveri, Vincenzo Turco; Journal of Solufrom n-octane to tion Chemistry; vol. 12; nb. 4; (1983); p. 221 - 232, View in Reaxys water at 25 deg to C

Enthalpy of Combustion (3) Enthalpy of Com- References bustion [Jmol-1] Lebedeva; Ryadnenko; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1382; ; p. 2442, View in Reaxys -1.41488E+06

Thomsen; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 52; (1905); p. 343; Thermochemische Untersuchungen; vol. 4; p. 104, View in Reaxys

-1.3494E+06

Berthelot; Matignon; Annales de Chimie (Cachan, France); vol. <6> 30; (1893); p. 557, View in Reaxys

Enthalpy of Formation (2) Enthalpy of ForTemperature (Enmation [Jmol-1] thalpy of Formation) [°C] 144026

24.85

References

Miroshnichenko; Vorob'eva; Russian Journal of Physical Chemistry A; vol. 73; nb. 3; (1999); p. 349 - 355, View in Reaxys Lebedeva; Ryadnenko; Russian Journal of Physical Chemistry; vol. 47; (1973); p.

1382; ; p. 2442, View in Reaxys

Enthalpy of Vaporization (2) Enthalpy of VaTemperature (Enporization thalpy of Vapori[Jmol-1] zation) [°C] 41449.3

Comment (Enthalpy of Vaporization)

24.85

37995.2

References

Miroshnichenko; Vorob'eva; Russian Journal of Physical Chemistry A; vol. 73; nb. 3; (1999); p. 349 - 355, View in Reaxys enthalpy of vapor- Goodeve; Transactions of the Faraday Society; vol. 30; (1934); p. ization:(aus 504; Chem. Zentralbl.; vol. 105; nb. II; (1934); p. 3228, Dampfdruckmes- View in Reaxys sungen).

Further Information (60) Description (Fur- References ther Information) Further information

Heintz et al.; Berichte der Bunsen-Gesellschaft; vol. 83; (1979); p. 926,927,928, View in Reaxys

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Further information

Beysens; Journal of Chemical Physics; vol. 71; (1979); p. 2557, View in Reaxys

Further information

Labowski; Acta Physica Polonica, A; vol. 56; (1979); p. 821,827, View in Reaxys

Further information

Norris; Randles; Australian Journal of Chemistry; vol. 32; (1979); p. 1487,1490, 1491, 1504, View in Reaxys

Further information

Shinkai et al.; Biopolymers; vol. 17; (1978); p. 2757,2758,2759, View in Reaxys

Further information

Petrula et al.; Journal of Chemical Physics; vol. 68; (1978); p. 623, View in Reaxys

Further information

Zhitomirskaya; Eremenko; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 27; (1978); p. 1595; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol.

27; (1978); p. 1822, View in Reaxys

Further information

Zioto; Chemical Physics Letters; vol. 53; (1978); p. 345, View in Reaxys

Further information

Chizhov et al.; Organic Mass Spectrometry; vol. 13; (1978); p. 611,612, View in Reaxys

Further information

Gibson; Canadian Journal of Chemistry; vol. 55; (1977); p. 2637,2638, View in Reaxys

Further information

Chan; Bruice; Journal of the American Chemical Society; vol. 99; nb. 20; (1977); p. 6721 - 6730, View in Reaxys

Further information

Laub; Purnell; Journal of the American Chemical Society; vol. 98; (1976); p. 30,31, View in Reaxys

Further information

Beyer; Lineberger; Journal of Chemical Physics; vol. 62; (1975); p. 4024, View in Reaxys

Further information

Greer; Hocken; Journal of Chemical Physics; vol. 63; (1975); p. 5067, View in Reaxys

Further information

Groner et al.; Chemical Physics; vol. 5; (1974); p. 136, View in Reaxys

Further information

Odokienko et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 47; (1974); p. 902,919, View in Reaxys

Further information

Vsetecka; Exner; Collection of Czechoslovak Chemical Communications; vol. 39; (1974); p. 1140,1143, 1147, View in Reaxys

Further information

Lorberth; Lange; Journal of Organometallic Chemistry; vol. 54; (1973); p. 165,167, 170, View in Reaxys

Further information

Lebedeva; Ryadnenko; Russian Journal of Physical Chemistry; vol. 47; (1973); p. 1382; ; p. 2442, View in Reaxys

Further information

Exner; Vsetecka; Tetrahedron Letters; (1972); p. 4613, View in Reaxys

Further information

Belyaev; Prokopovich; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 1599,1661, View in Reaxys

Further information

Reid; Tucker; Journal of the Chemical Society [Section] D: Chemical Communications; (1970); p. 1286, View in Reaxys

Further information

Witanowski; Shevelev; Journal of Molecular Spectroscopy; vol. 33; (1970); p. 19,20, View in Reaxys

Further information

Fukuyama,M. et al.; Journal of the American Chemical Society; vol. 92; (1970); p. 4689 - 4699, View in Reaxys

Further information

Koshtoyan et al.; Doklady Chemistry; vol. 185; (1969); p. 285; Dokl. Akad. Nauk SSSR Ser. Khim.; vol. 185; (1969); p. 837, View in Reaxys

Further information

Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 17; (1969); p. 2049,2050, View in Reaxys

Further information

Chandra; Nath; Journal of Chemical Physics; vol. 51; (1969); p. 5299, View in Reaxys

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Further information

Brookes; Jonathan; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 25; (1969); p. 187,188, View in Reaxys

Further information

Ostaszynski et al.; Tetrahedron; vol. 25; (1969); p. 1929,1936, View in Reaxys

Further information

Tsuda et al.; Bulletin of the Chemical Society of Japan; vol. 42; (1969); p. 614, View in Reaxys

Further information

Ivanova et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1968); p. 2038; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1968); p. 2144, View in Reaxys

Further information

Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 2120, View in Reaxys

Further information

Fraser; Paul; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 1407, View in Reaxys

Further information

Nelson et al.; Journal of Physical Chemistry; vol. 71; (1967); p. 2742, View in Reaxys

Further information

Griffith et al.; Journal of the Chemical Society [Section] B: Physical Organic; (1967); p. 533, View in Reaxys

Further information

Spokes; Benson; Journal of the American Chemical Society; vol. 89; (1967); p. 6030,6034, View in Reaxys

Further information

Sinha et al.; Indian Journal of Physics (1926-1976); vol. 41; (1967); p. 183,194, View in Reaxys

Further information

Liu; Ziegler; Journal of Chemical and Engineering Data; vol. 11; (1966); p. 187, View in Reaxys

Further information

Zapior,B.; Sliwa,B.; Roczniki Chemii; vol. 39; (1965); p. 1461 - 1468, View in Reaxys

Further information

Griswold; Starcher; Journal of Organic Chemistry; vol. 30; (1965); p. 1687,1690, View in Reaxys

Further information

Aplin et al.; Journal of the American Chemical Society; vol. 87; (1965); p. 4888,4889, View in Reaxys

Further information

Armand; Bulletin de la Societe Chimique de France; (1965); p. 3246,3253, View in Reaxys

Further information

Witanowski et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2569,2570, View in Reaxys

Further information

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys

Further information

Isaguljanz; Markosjan; J. Appl. Chem. USSR (Engl. Transl.); vol. 37; (1964); p. 1145,1146, View in Reaxys

Further information

Isaguljanz; Poredda; J. Appl. Chem. USSR (Engl. Transl.); vol. 37; (1964); p. 1093,1092, View in Reaxys

Further information

Hofman et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 554,555, View in Reaxys

Further information

Geiseler; Kessler; Berichte der Bunsen-Gesellschaft; vol. 68; (1964); p. 571, View in Reaxys

Further information

Komarowa; Kogan; J. Appl. Chem. USSR (Engl. Transl.); vol. 37; (1964); p. 1776,1764, View in Reaxys

Further information

Kornblum,N.; Brown,R.A.; Journal of the American Chemical Society; vol. 86; (1964); p. 2681 - 2687, View in Reaxys

Further information

Feuer,H. et al.; Spectrochimica Acta; vol. 19; (1963); p. 431 - 434, View in Reaxys

Further information

Schwetlick et al.; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 113,119, View in Reaxys

Further information

Kornblum,N.; Brown,R.A.; Journal of the American Chemical Society; vol. 85; (1963); p. 1359 - 1360, View in Reaxys

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Further information

Pesez et al.; Bulletin de la Societe Chimique de France; (1962); p. 719, View in Reaxys

Further information

Buczkowski; Urbanski; Spectrochimica Acta; vol. 18; (1962); p. 1187,1188, 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

Francois; Bulletin de la Societe Chimique de France; (1962); p. 511, View in Reaxys

Further information

Klimowa; SaGrodina; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1961); p. 160; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1961); p. 176, View in Reaxys

Further information

Freymann; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 253; (1961); p.

2061,2062, View in Reaxys

Further information

Balasubramanian; Rao; Chemistry and Industry (London, United Kingdom); (1960); p. 1025, View in Reaxys

Heat Capacity Cp (1) Heat Capacity Cp Temperature [Jmol-1K-1] (Heat Capacity Cp) [°C] 130.88

-73.1

Ionization Potential (2) Ionization Poten- Method (Ionizatial [eV] tion Potential) 11.09

PE

References

Dvorkin, P. L.; Ryzhova, G. L.; Lebedev, Yu. A.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 33; (1984); p. 982 987; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 5; (1984); p. 1069 1074, View in Reaxys Comment (Ioniza- References tion Potential) Higher potentials: 11.54, 13.39, 14.20, 14.87, 15.90, 17.15 eV

Mok, C. Y.; Kok, L. Y.; Chin, W. S.; Huang, H. H.; Journal of Molecular Structure; vol. 175; (1988); p. 429 - 434, View in Reaxys

Gibson; Canadian Journal of Chemistry; vol. 55; (1977); p.

2637,2638, View in Reaxys; Watanabe et al.; Journal of Quantitative Spectroscopy and Radiative Transfer; vol. 2; (1962); p. 369,377, View in Reaxys Liquid Phase (2) Description (Liquid Phase)

References

Structure of the liquid

Demidov; Libov; Russian Journal of Physical Chemistry A; vol. 71; nb. 12; (1997); p. 1997 - 1999, View in Reaxys

Association in the liquid state

Demidov; Libov; Russian Journal of Physical Chemistry A; vol. 71; nb. 12; (1997); p. 1997 - 1999, View in Reaxys

Liquid/Liquid Systems (MCS) (35) 1 of 35

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

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

5.81 - 6.65

Partner (Liquid/Liquid Systems (MCS))

polystyrene(h8), Mw = 13502

De Sousa, Herminio C.; Rebelo, Luis P. N.; Journal of Chemical Thermodynamics; vol. 32; nb. 3; (2000); p. 355 387, View in Reaxys 2 of 35

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

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

48.69 - 50.09

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Partner (Liquid/Liquid Systems (MCS))

polystyrene(h8), Mw = 129200

De Sousa, Herminio C.; Rebelo, Luis P. N.; Journal of Chemical Thermodynamics; vol. 32; nb. 3; (2000); p. 355 387, View in Reaxys 3 of 35

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

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

42.19 - 43.59

Partner (Liquid/Liquid Systems (MCS))

polystyrene(h8), Mw = 90100

De Sousa, Herminio C.; Rebelo, Luis P. N.; Journal of Chemical Thermodynamics; vol. 32; nb. 3; (2000); p. 355 387, View in Reaxys 4 of 35

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Partner (Liquid/Liquid Systems (MCS))

polystyrene(h8), Mw = 30740

De Sousa, Herminio C.; Rebelo, Luis P. N.; Journal of Chemical Thermodynamics; vol. 32; nb. 3; (2000); p. 355 387, View in Reaxys 5 of 35

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Partner (Liquid/Liquid Systems (MCS))

chloroform

Barril; Munoz; Luque; Orozco; Physical Chemistry Chemical Physics; vol. 2; nb. 21; (2000); p. 4897 - 4905, View in Reaxys 6 of 35

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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

77.13 - 113.85

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

759.811

Partner (Liquid/Liquid Systems (MCS))

ethyl acetate

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 7 of 35

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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

101.54 - 113.85

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

759.811

Partner (Liquid/Liquid Systems (MCS))

1-Propyl acetate

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 8 of 35

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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

88.6 - 113.85

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

759.811

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Partner (Liquid/Liquid Systems (MCS))

Isopropyl acetate

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 9 of 35

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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

79.56 - 113.85

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

759.811

Partner (Liquid/Liquid Systems (MCS))

propanoic acid methyl ester

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 10 of 35

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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

99.08 - 113.85

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

759.811

Partner (Liquid/Liquid Systems (MCS))

ethyl propionate

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 11 of 35

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

gas

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

39.2

Partner (Liquid/Liquid Systems (MCS))

apolane

Weckwerth, Jeff D.; Carr, Peter W.; Vitha, Mark F.; Nasehzadeh, Asad; Analytical Chemistry; vol. 70; nb. 17; (1998); p. 3712 - 3716, View in Reaxys 12 of 35

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Partner (Liquid/Liquid Systems (MCS))

cetane; 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 13 of 35

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

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

29

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

759.8

Partner (Liquid/Liquid Systems (MCS))

2,2,4-trimethylpentane

Battler, John R.; Rowley, Richard L.; Journal of Chemical & Engineering Data; vol. 35; nb. 3; (1990); p. 334 - 338, View in Reaxys

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14 of 35

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

Partner (Liquid/Liquid Systems (MCS))

1-Octanol

Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Marcus, Yizhak; Taft, Robert W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5244 - 5255, View in Reaxys 15 of 35

Description (Liquid/ Liquid Systems (MCS))

Temperature of separation

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

28.7 - 29.2

Partner (Liquid/Liquid Systems (MCS))

2,2,4-trimethylpentane

Schroer; Rybarsch; Strojny; Staude; Berichte der Bunsengesellschaft/Physical Chemistry Chemical Physics; vol.

92; nb. 8; (1988); p. 846 - 850, View in Reaxys 16 of 35

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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

29 - 33

Partner (Liquid/Liquid Systems (MCS))

ethylene glycol; cyclohexane; methanol

Rzoska, S. J.; Chrapec, J.; Ziolo, J.; Journal of Chemical Physics; vol. 84; nb. 3; (1986); p. 1735 - 1738, View in Reaxys 17 of 35

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Solvent (Liquid/Liquid Systems (MCS))

H2O

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

25

Partner (Liquid/Liquid Systems (MCS))

oleyl alcohol

Kuehne; Bocek; Scharfenberg; Frank; European Journal of Medicinal Chemistry; vol. 16; nb. 1; (1981); p. 7 - 12, View in Reaxys 18 of 35

Description (Liquid/ Liquid Systems (MCS))

Liquid/liquid phase diagram

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

6.9 - 26.9

Partner (Liquid/Liquid Systems (MCS))

1-Decanol

Baranowska-Majgier, Helena; Pyzuk, Wieslaw; Jeute, Wojciech; Ziolo, Jerzy; Journal of Chemical & Engineering Data; vol. 26; nb. 1; (1981); p. 51 - 53, View in Reaxys 19 of 35

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

hexane

Ziovo, J.; Ziejewska, Z.; Piotrowska, J.; Journal of Physical Chemistry; vol. 84; nb. 9; (1980); p. 979 - 980, View in Reaxys 20 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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Partner (Liquid/Liquid Systems (MCS))

nitrobenzene; hexane

Ziovo, J.; Ziejewska, Z.; Piotrowska, J.; Journal of Physical Chemistry; vol. 84; nb. 9; (1980); p. 979 - 980, View in Reaxys 21 of 35

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Balasubramanian; Mitra; Journal of Physical Chemistry; vol. 83; (1979); p. 2724, View in Reaxys; Clever et al.; Journal of Chemical and Engineering Data; vol. 17; (1972); p. 31,33, View in Reaxys; Greer et al.; Physical Review Letters; vol. 34; (1975); p. 250, View in Reaxys 22 of 35

Description (Liquid/ Liquid Systems (MCS))

Distribution between solvent 1 + 2

Duraiswamy; Minard; Journal of Chemical and Engineering Data; vol. 18; (1973); p. 203,204,205, View in Reaxys; Buchowski; Teperek; Roczniki Chemii; vol. 45; (1971); p. 1329,1330, View in Reaxys 23 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Wims et al.; Journal of Chemical Physics; vol. 50; (1969); p. 619, View in Reaxys 24 of 35

Description (Liquid/ Liquid Systems (MCS))

Equilibrium of liquid phases

Malone; Vining; Journal of Chemical and Engineering Data; vol. 12; (1967); p. 387, View in Reaxys 25 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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

25 - 30

Partner (Liquid/Liquid Systems (MCS))

2,2,4-trimethylpentane

Vreeland; Dunlap; Journal of Physical Chemistry; vol. 61; (1957); p. 329,331, View in Reaxys 26 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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

25 - 51.3

Partner (Liquid/Liquid Systems (MCS))

2,2,4-trimethylpentane; Perfluorotributylamine

Vreeland; Dunlap; Journal of Physical Chemistry; vol. 61; (1957); p. 329,331, View in Reaxys 27 of 35

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-Decanol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 28 of 35

Description (Liquid/ Liquid Systems (MCS))

Critical solution temperature

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 29 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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

0 - 10

Partner (Liquid/Liquid Systems (MCS))

1-Decanol; ethylene glycol

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Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 30 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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

14 - 24

Partner (Liquid/Liquid Systems (MCS))

1-dodecyl alcohol; ethylene glycol

Francis; Journal of Physical Chemistry; vol. 60; (1956); p. 20,25, View in Reaxys 31 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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

21 - 26

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

47808

Partner (Liquid/Liquid Systems (MCS))

carbon dioxide; cetane

Francis; Journal of Physical Chemistry; vol. 58; (1954); p. 1099,1104, View in Reaxys 32 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

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

21 - 26

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

47808

Partner (Liquid/Liquid Systems (MCS))

carbon dioxide; decalin

Francis; Journal of Physical Chemistry; vol. 58; (1954); p. 1099,1104, View in Reaxys 33 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Comment (Liquid/Liquid Systems (MCS))

mit normalen primaeren Alkoholen aus der Reihe 10 bis 18.

Hoerr; Harwood; Ralston; Journal of Organic Chemistry; vol. 9; (1944); p. 270, View in Reaxys 34 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Comment (Liquid/Liquid Systems (MCS))

mit normalen Fettsaeuren aus der Reihe 7 bis 17.

Hoerr; Ralston; Journal of Organic Chemistry; vol. 9; (1944); p. 355, View in Reaxys 35 of 35

Description (Liquid/ Liquid Systems (MCS))

Solution equilibrium

Comment (Liquid/Liquid Systems (MCS))

mit Nitrilen normaler Fettsaeuren aus der Reihe 9 bis 17.

Hoerr et al.; Journal of Organic Chemistry; vol. 9; (1944); p. 75, View in Reaxys Liquid/Vapour Systems (MCS) (53) 1 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

2-methyl-heptane

Jacob; Anisimov; Sengers; Oleinikova; Weingaertner; Kumar; Physical Chemistry Chemical Physics; vol. 3; nb.

5; (2001); p. 829 - 831, View in Reaxys

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2 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 77.13 - 113.85 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 759.811 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethyl acetate

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 3 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 101.54 - 113.85 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 759.811 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

1-Propyl acetate

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 4 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 88.6 - 113.85 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 759.811 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

Isopropyl acetate

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 5 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 79.56 - 113.85 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 759.811 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

propanoic acid methyl ester

Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 6 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Temperature (Liquid/ 99.08 - 113.85 Vapour Systems (MCS)) [°C] Pressure (Liquid/Vapour 759.811 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

ethyl propionate

Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.

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Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 271 - 273, View in Reaxys 7 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

cetane

Dallas, Andrew J.; Carr, Peter W.; Journal of Physical Chemistry; vol. 98; nb. 18; (1994); p. 4927 - 4939, View in Reaxys 8 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Kawate, Kohichiro; Nakata, Mitsuo; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 166; nb. 2; (1990); p. 195 - 209, View in Reaxys 9 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

cyclohexane

Johnson, K. A.; Journal of Chemical Thermodynamics; vol. 20; nb. 7; (1988); p. 889 - 896, View in Reaxys; Marsh, K. N.; Rogers, H.; Journal of Chemical Thermodynamics; vol. 21; nb. 2; (1989); p. 211 - 218, View in Reaxys 10 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

3-methyl-pentane

Berg, Robert F.; Moldover, Michael R.; Journal of Chemical Physics; vol. 89; nb. 6; (1988); p. 3694 - 3704, View in Reaxys 11 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

octanol

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 12 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] 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 13 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

ethanol

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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 14 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] 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 15 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 25 Vapour Systems (MCS)) [°C] 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 16 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

n-heptane

Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys; Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 17 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1-heptene

Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys 18 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,6--heptadiene

Afrashtehfar, Shapour; Cave, Genille C. B.; Canadian Journal of Chemistry; vol. 64; (1986); p. 198 - 203, View in Reaxys 19 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Temperature (Liquid/ 23.3 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

cyclohexane

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Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 20 of 53

Description (Liquid/ Boiling point diagram Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

palladium-rhodium

Grishina, T. M.; Russian Journal of Physical Chemistry; vol. 58; nb. 11; (1984); p. 1694 - 1697; Zhurnal Fizicheskoi Khimii; vol. 58; (1984); p. 2797 - 2800, View in Reaxys 21 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

benzene

Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 22 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 20 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

tetrachloromethane

Milanova, Etela; Cave, Genille C.; Canadian Journal of Chemistry; vol. 60; (1982); p. 2697 - 2706, View in Reaxys 23 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) 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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) 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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) 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 26 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) 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 27 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

chloroform

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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28 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

dichloromethane

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

methanol

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethyl bromide

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

ethyl iodide

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) 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 33 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

1-Chloropropane

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

tertiary 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 35 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

isoprene

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

1-penten

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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 37 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

2-methyl-2- butene

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

pentane

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) 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 40 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

cyclohexane

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 41 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

hexane

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 42 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 45.4 - 81.1 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

1,2-DICHLOROETHANE

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 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Temperature (Liquid/ 24.9 - 66.3 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

hexane

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 44 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS))

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Temperature (Liquid/ 69.6 - 107.9 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

toluene

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 45 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Partner (Liquid/Vapour Systems (MCS))

2-Methylpentane

McLure, Ian A.; Pegg, Ian L.; Journal of Molecular Structure; vol. 80; (1982); p. 393 - 400, View in Reaxys 46 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Temperature (Liquid/ 26 Vapour Systems (MCS)) [°C] Partner (Liquid/Vapour Systems (MCS))

3-methyl-pentane

Wood, Kurt A.; Strauss, Herbert L.; Journal of Chemical Physics; vol. 74; nb. 11; (1981); p. 6027 - 6036, View in Reaxys 47 of 53

Description (Liquid/ Vapour pressure diagram for the mixture Vapour Systems (MCS)) Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys

48 of 53

Description (Liquid/ Critical data for mixtures Vapour Systems (MCS)) Fischer et al.; Pharmazeutische Zentralhalle; vol. 105; (1966); p. 73,74, View in Reaxys; Das; Griffiths; Journal of Chemical Physics; vol. 70; (1979); p. 5555, View in Reaxys; Malecki; Ziolo; Chemical Physics; vol. 35; (1978); p.

187, View in Reaxys

49 of 53

Description (Liquid/ Activity coefficients of the components in the mixture Vapour Systems (MCS)) Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys; Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys

50 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Gorbunov; Susarev; J. Appl. Chem. USSR (Engl. Transl.); vol. 41; (1968); p. 2680,2522, View in Reaxys; Orye; Prausnitz; Transactions of the Faraday Society; vol. 61; (1965); p. 1338,1340, View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 38; (1965); p. 2617,2558, View in Reaxys

51 of 53

Description (Liquid/ Boiling points of mixtures Vapour Systems (MCS)) Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys

52 of 53

Description (Liquid/ Liquid/vapour equilibrium Vapour Systems (MCS)) Pressure (Liquid/Vapour 54.6 - 400 Systems (MCS)) [Torr] Partner (Liquid/Vapour Systems (MCS))

nitromethane

Cantoni; Feldman; Industrial and Engineering Chemistry; vol. 45; (1953); p. 2580, View in Reaxys 53 of 53

Description (Liquid/ Boiling points of mixtures Vapour Systems (MCS)) Comment (Liquid/ molekulare Siedepunktserhoehung:25.5.

Vapour Systems (MCS))

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Beckmann; Fuchs; Gernhardt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 18; (1895); p. 512, View in Reaxys Magnetic Susceptibility (1) References Pascal; Bulletin de la Societe Chimique de France; vol. <4>9; (1911); p. 339; Annales de Chimie (Cachan, France); vol. <8>25; (1912); p. 352, View in Reaxys; Francois; Bulletin de la Societe Chimique de France; (1962); p. 511, View in Reaxys Mechanical & Physical Properties (MCS) (26) 1 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

20 - 40

Partner (Mechanical & Physical Properties (MCS))

methanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 2 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

20 - 40

Partner (Mechanical & Physical Properties (MCS))

ethanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 3 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

20 - 40

Partner (Mechanical & Physical Properties (MCS))

propan-1-ol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 4 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

20 - 40

Partner (Mechanical & Physical Properties (MCS))

isopropyl alcohol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 5 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

20 - 40

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Partner (Mechanical & Physical Properties (MCS))

iso-butanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 6 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

25 - 40

Partner (Mechanical & Physical Properties (MCS))

tert-butanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 7 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

10 - 35

Partner (Mechanical & Physical Properties (MCS))

butan-1-ol

Romani; Troncoso; Carballo; Cerdeirina; Gonzalez; Journal of Chemical and Engineering Data; vol. 45; nb. 4; (2000); p. 594 - 599, View in Reaxys 8 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

10 - 35

Partner (Mechanical & Physical Properties (MCS))

i-Butyl alcohol

Romani; Troncoso; Carballo; Cerdeirina; Gonzalez; Journal of Chemical and Engineering Data; vol. 45; nb. 4; (2000); p. 594 - 599, View in Reaxys 9 of 26

Description (Mechanical & Physical Properties (MCS))

Excess partial molal volume

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

10 - 35

Partner (Mechanical & Physical Properties (MCS))

iso-butanol

Romani; Troncoso; Carballo; Cerdeirina; Gonzalez; Journal of Chemical and Engineering Data; vol. 45; nb. 4; (2000); p. 594 - 599, View in Reaxys 10 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

20 - 40

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Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

acetic acid methyl ester

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 11 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

ethyl acetate

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 12 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

1-Propyl acetate

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 13 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

20 - 40

Pressure (Mechanical & Physical Properties (MCS)) [Torr]

760

Partner (Mechanical & Physical Properties (MCS))

ethyl propionate

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 14 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

20

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Partner (Mechanical & Physical Properties (MCS))

benzene

Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 15 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

20

Partner (Mechanical & Physical Properties (MCS))

para-xylene

Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 16 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

20

Partner (Mechanical & Physical Properties (MCS))

mesitylene

Yadava, Raja R.; Singh, Vishwanath; Yadava, Sarvanand S.; Journal of Chemical & Engineering Data; vol. 39; nb. 4; (1994); p. 705 - 707, View in Reaxys 17 of 26

Description (Mechanical & Physical Properties (MCS))

Partial molal volume

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

25

Partner (Mechanical & Physical Properties (MCS))

hexane

Cordray, James H.; Eckert, Charles A.; Journal of Chemical & Engineering Data; vol. 32; nb. 1; (1987); p. 83 - 85, View in Reaxys 18 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

30

Partner (Mechanical & Physical Properties (MCS))

1-Octanol

Dewan, R. K.; Mehta, S. K.; Journal of Chemical Thermodynamics; vol. 18; nb. 2; (1986); p. 101 - 106, View in Reaxys 19 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

30

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Partner (Mechanical & Physical Properties (MCS))

ethylbenzene

Dewan, R. K.; Mehta, S. K.; Journal of Chemical Thermodynamics; vol. 18; nb. 11; (1986); p. 1015 - 1020, View in Reaxys 20 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

45

Partner (Mechanical & Physical Properties (MCS))

cyclohexane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 21 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

25 - 45

Partner (Mechanical & Physical Properties (MCS))

tetrachloromethane

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 22 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

25

Partner (Mechanical & Physical Properties (MCS))

para-xylene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 23 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

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

25

Partner (Mechanical & Physical Properties (MCS))

benzene

Marsh, Kenneth N.; Journal of Chemical Thermodynamics; vol. 17; nb. 1; (1985); p. 29 - 42, View in Reaxys 24 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Handa et al.; Journal of Chemical Thermodynamics; vol. 9; (1977); p. 451,459, View in Reaxys; Reeder et al.; Journal of Chemical Thermodynamics; vol. 8; (1976); p. 133,134, 135, View in Reaxys; Anderson et al.; AIChE Journal; vol. 8; (1962); p. 66,67, View in Reaxys 25 of 26

Description (Mechanical & Physical Properties (MCS))

Virial coefficients

Vigdergauz; Semkin; Russian Journal of Physical Chemistry; vol. 45; (1971); p. 518,519; ; p. 931, View in Reaxys

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26 of 26

Description (Mechanical & Physical Properties (MCS))

Volume change on mixing

Partner (Mechanical & Physical Properties (MCS))

Glutaronitrile

Phibbs; Journal of Physical Chemistry; vol. 59; (1955); p. 346,249, View in Reaxys Mechanical Properties (5) Description (MeReferences chanical Properties) Molar volume

Dewan, R.K.; Sharma, A.K.; Mehta, S.K.; Journal of Solution Chemistry; vol. 17; nb. 5; (1988); p. 459 - 466, View in Reaxys; Taft; Abraham; Famini; Doherty; Abboud; Kamlet; Journal of Pharmaceutical Sciences; vol. 74; nb. 8; (1985); p. 807 - 814, View in Reaxys; Ruelle; Buchmann; Kesselring; Journal of Pharmaceutical Sciences; vol. 83; nb. 3; (1994); p. 396 - 403, View in Reaxys

Virial coefficients of the equation of state

Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p. 897,899 - 901, View in Reaxys

PVT Relationship

Gupta; Hanks; Thermochimica Acta; vol. 21; (1977); p. 143,148,150,151, View in Reaxys; Hanks et al.; Thermochimica Acta; vol. 23; (1978); p. 57,62, 63, View in Reaxys

Viscosity

Stein et al.; Journal of Chemical Physics; vol. 56; (1972); p. 6164, View in Reaxys; Tsai et al.; Journal of Chemical Physics; vol. 58; (1973); p. 4582, View in Reaxys; Honda; Sasada; Japanese Journal of Applied Physics; vol. 16; (1977); p. 1775,1776-1778, View in Reaxys; Chandra; Nath; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 1614, View in Reaxys; Tsai; Mcintyre; Journal of Chemical Physics; vol. 60; (1974); p. 937, View in Reaxys; Schiavo; Marrosu; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 105; (1977); p. 157,162, 164, 166, View in Reaxys

Compressibility

Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys

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

Groner et al.; Chemical Physics; vol. 11; (1975); p. 63,65,68,69-71,79, View in Reaxys; Popov; Shlyapochnikov; Optics and Spectroscopy; vol. 15; (1963); p. 174; ; p. 325, View in Reaxys

Fundamental vibrations

Varsanyi et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p.

1205,1210, View in Reaxys

Optics (4) Description (Optics)

References

Rayleigh scattering

Derrick; Clever; Journal of Physical Chemistry; vol. 75; (1971); p. 3728, View in Reaxys; Zalczer, G.; Beysens, D.; Journal of Chemical Physics; vol. 72; nb. 1; (1980); p. 348 - 352, View in Reaxys

Diffraction

Beysens; Wesfrised; Journal of Chemical Physics; vol. 71; (1979); p. 119, View in Reaxys; Beysens; Calmettes; Journal of Chemical Physics; vol. 66; (1977); p. 766, View in Reaxys

Magnetic circular dichroism

Barth et al.; Journal of the Chemical Society, Chemical Communications; (1975); p. 672, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys

Magnetorotation

Perkin; Journal of the Chemical Society; vol. 55; (1889); p. 748, View in Reaxys; Bonnafous; Labarre; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1376, View in Reaxys

Other Thermochemical Data (6) Description (Oth- Comment (Other er Thermochemi- Thermochemical cal Data) Data)

References

Entropy

Goffredi, Mario; Liszi, Janos; Nemeth, Bela; Liveri, Vincenzo Turco; Journal of Solution Chemistry; vol. 12; nb. 4; (1983); p. 221 - 232, View in Reaxys

Thermodynamic properties

Gilbert; Treuwith; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 2010,2013, View in Reaxys; Cumming; Kebarle; Journal of the American Chemical Society; vol. 100; (1978); p. 1835,1836, View in Reaxys; Czworniak et al.; Chemical Physics; vol. 11; (1975); p. 451,466,469, View in Reaxys

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Enthalpy

Pivina et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 26; (1977); p. 158; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 26; (1977); p. 182, View in Reaxys; Belik; Shlyapochnikov; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 26; (1977); p. 2585; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 26; (1977); p. 2795, View in Reaxys

Heat of combustion at constant volume

bei 26.7grad: 326.7 kcal*molE-1.

Cass et al.; Journal of the Chemical Society; (1958); p. 958,960, View in Reaxys

Heat of combustion at constant volume

bei 25grad 325.8 kcal/Mol.

Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys

Heat of combustion at constant volume

322.45 Cal/Mol.

Berthelot; Matignon; Annales de Chimie (Cachan, France); vol. <6> 30; (1893); p. 557, View in Reaxys

Solubility (MCS) (8) 1 of 8

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 2 of 8

Saturation

in pure solvent

Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Carr, Peter W.; Doherty, Robert F.; Taft, Robert W.; Journal of Physical Chemistry; vol. 91; nb. 7; (1987); p. 1996 - 2004, View in Reaxys; Kamlet, Mortimer J.; Doherty, Ruth M.; Abraham, Michael H.; Marcus, Yizhak; Taft, Robert W.; Journal of Physical Chemistry; vol. 92; nb. 18; (1988); p. 5244 - 5255, View in Reaxys; Valvani; Yalkowsky; Roseman; Journal of Pharmaceutical Sciences; vol. 70; nb. 5; (1981); p. 502 - 507, View in Reaxys; Kamlet; Doherty; Abboud; Abraham; Taft; Journal of Pharmaceutical Sciences; vol. 75; nb. 4; (1986); p. 338 - 349, View in Reaxys 3 of 8

Comment (Solubility (MCS))

geloest in 3-Methylpentan

Chang et al.; Berichte der Bunsen-Gesellschaft; vol. 76; (1972); p. 260,263, View in Reaxys 4 of 8

Comment (Solubility (MCS))

Loesungstemp. m. Isooctan; Konzentrationsfluktuation m. Isooctan

Shakhparonov et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 1425; ; p. 2543, View in Reaxys 5 of 8

Comment (Solubility (MCS))

gegenseitige Loeslichkeit in den ternaeren Systemen mit Octan u. Oct-1-en sowie mit Octan u. 2,2,4-Trimethyl-pentan

Hwa et al.; Journal of Chemical and Engineering Data; vol. 8; (1963); p. 409, View in Reaxys 6 of 8

Comment (Solubility (MCS))

gegenseitige Loeslichkeit in binaeren Systemen mit Hexan, 2-Methyl-pentan, Hex-1-en, Oct-1-en, Octan, 2,2,4-Trimethyl-pentan u. Decan

Hwa et al.; Journal of Chemical and Engineering Data; vol. 8; (1963); p. 409, View in Reaxys 7 of 8

Temperature (Solubility (MCS)) [°C]

25

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

9.99999E-02 ml solvent dissolves. 2.6 ml Substance.

Booth; Everson; Industrial and Engineering Chemistry; vol. 40; (1948); p. 1491,1492; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2627,2628, View in Reaxys 8 of 8

Temperature (Solubility (MCS)) [°C]

20

Solvent (Solubility (MCS))

H2O

Comment (Solubility (MCS))

9.99999E-02 ml solvent dissolves. 4.5 ml Substance.

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Ericsson; Industrial and Engineering Chemistry; vol. 35; (1943); p. 1028, View in Reaxys Solution Behaviour (MCS) (3) 1 of 3

Description (Solution Behaviour (MCS))

Solubility [Henry constant]

Temperature (Solution Behaviour (MCS)) [°C]

20 - 50

Partner (Solution Behaviour (MCS))

H2O

Dohnal; Benes; Journal of Chemical and Engineering Data; vol. 44; nb. 5; (1999); p. 1097 - 1102, View in Reaxys 2 of 3

Description (Solution Behaviour (MCS))

Mutual solubility

Temperature (Solution Behaviour (MCS)) [°C]

0 - 90.1

Partner (Solution Behaviour (MCS))

H2O

Stephenson; Journal of Chemical and Engineering Data; vol. 37; nb. 1; (1992); p. 80 - 95, View in Reaxys 3 of 3

Description (Solution Behaviour (MCS))

Dissolving capacity

Temperature (Solution Behaviour (MCS)) [°C]

20

Comment (Solution Behaviour (MCS))

100 ml Nitroaethan loest 0.9 ml.

Partner (Solution Behaviour (MCS))

water

Ericsson; Industrial and Engineering Chemistry; vol. 35; (1943); p. 1028, View in Reaxys Sound Properties (2) Description Comment (Sound (Sound ProperProperties) ties) Velocity of sound

temperature dependence

References

Romani; Troncoso; Carballo; Cerdeirina; Gonzalez; Journal of Chemical and Engineering Data; vol. 45; nb. 4; (2000); p. 594 - 599, View in Reaxys

Ultrasonic properties

Shakhparonov et al.; Russian Journal of Physical Chemistry; vol. 43; (1969); p. 1425; ; p. 2543, View in Reaxys

Static Dielectric Constant (1) Static Dielectric Temperature Constant (Static Dielectric Constant) [°C]

References

34.8

25

Surface Tension (4) Surface Tension Temperature [g·s-2] (Surface Tension) [°C]

Schmid, R.; Journal of Solution Chemistry; vol. 12; nb. 2; (1983); p. 135 - 152, View in Reaxys References

Walden; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 66; (1909); p. 387, View in Reaxys; Snead; Clever; Journal of Chemical and Engineering Data; vol. 7; (1962); p. 393, View in Reaxys 32.14 - 87.3

20.2 - 24

Vogel; Journal of the Chemical Society; (1948); p. 1809,1811, 1813; Chem.Abstr.; (1946); p. 5066, View in Reaxys

31.3

20

Ericsson; Industrial and Engineering Chemistry; vol. 35; (1943); p. 1028, View in Reaxys

31.31

25

Boyd; Copeland; Journal of the American Chemical Society; vol. 64; (1942); p. 2542, View in Reaxys

Transport Data (1) Description References (Transport Data)

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Thermal conductivity

Sakiadis; Coates; A.I.Ch.E.Journal; vol. 1; (1955); p. 275,277, View in Reaxys

Transport Phenomena (MCS) (18) 1 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

methanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 2 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

ethanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 3 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

propan-1-ol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 4 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

isopropyl alcohol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 5 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

iso-butanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 6 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 25 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

tert-butanol

Tu; Liu; Wang; Chou; Journal of Chemical and Engineering Data; vol. 45; nb. 3; (2000); p. 450 - 456, View in Reaxys 7 of 18

Description (Transport Phenomena (MCS))

Viscosity

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Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

acetic acid methyl ester

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 8 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

ethyl acetate

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 9 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

1-Propyl acetate

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 10 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Pressure (Transport Phenomena (MCS)) [Torr]

760

Partner (Transport Phenomena (MCS))

ethyl propionate

Liu, Chien-Yun; Ku, Hsu-Chen; Tu, Chein-Hsiun; Journal of Chemical and Engineering Data; vol. 44; nb. 2; (1999); p. 360 - 364, View in Reaxys 11 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

benzene

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb.

4; (1988); p. 402 - 404, View in Reaxys 12 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C]

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Partner (Transport Phenomena (MCS))

para-xylene

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb.

4; (1988); p. 402 - 404, View in Reaxys 13 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

mesitylene

Yadava, Raja R.; Yadava, Sarvanand S.; Singh, Vishwa N.; Journal of Chemical & Engineering Data; vol. 33; nb.

4; (1988); p. 402 - 404, View in Reaxys 14 of 18

Description (Transport Phenomena (MCS))

Viscosity

Partner (Transport Phenomena (MCS))

3-methyl-pentane

Berg, Robert F.; Moldover, Michael R.; Journal of Chemical Physics; vol. 89; nb. 6; (1988); p. 3694 - 3704, View in Reaxys 15 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 31.9 - 54.9 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

ethylene glycol; cyclohexane; methanol

Rzoska, S. J.; Chrapec, J.; Ziolo, J.; Journal of Chemical Physics; vol. 84; nb. 3; (1986); p. 1735 - 1738, View in Reaxys 16 of 18

Description (Transport Phenomena (MCS))

Viscosity

Temperature (Transport 20 - 40 Phenomena (MCS)) [°C] Partner (Transport Phenomena (MCS))

2-Methylpentane

McLure, Ian A.; Pegg, Ian L.; Journal of Molecular Structure; vol. 80; (1982); p. 393 - 400, View in Reaxys 17 of 18

Description (Transport Phenomena (MCS))

Diffusion

Stein et al.; Journal of Chemical Physics; vol. 56; (1972); p. 6164, View in Reaxys; Gorring; Journal of Catalysis; vol. 31; (1973); p. 13,21, View in Reaxys; Evanoff; Harris; Canadian Journal of Chemistry; vol. 56; (1978); p. 574, View in Reaxys; Czworniak et al.; Chemical Physics; vol. 11; (1975); p. 451,466,469, View in Reaxys 18 of 18

Description (Transport Phenomena (MCS))

Viscosity

Stein et al.; Journal of Chemical Physics; vol. 55; (1971); p. 4265, View in Reaxys Vapour Pressure (6) Vapour Pressure Temperature (Va[Torr] pour Pressure) [°C] 45.7321 - 248.35

Comment (Vapour Pressure)

40 - 80

References

Giles, Neil F.; Wilson, Grant M.; Journal of Chemical and Engineering Data; vol. 51; nb. 6; (2006); p. 1966 - 1972, View in Reaxys Hodge; Industrial and Engineering Chemistry; vol. 32; (1940); p.

748, View in Reaxys; Saunders; Spaull; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 28; (1961); p. 332,337, View in Reaxys; Komarova; Kogan; J. Appl. Chem. USSR (Engl.

Transl.); vol. 38; (1965); p. 2690,2629,2630, View in Reaxys; Marsh et al.; Journal of Chemical Thermodynamics; vol. 11; (1979); p.

897,899 - 901, View in Reaxys

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equation exists.

Toops; Journal of Physical Chemistry; vol. 60; (1956); p. 304, View in Reaxys

15.6

20

v.Schickh; Angewandte Chemie; vol. 62; (1950); p. 547,554, View in Reaxys

8.52 - 676.6

10 - 110

Holcomb; Dorsey; Industrial and Engineering Chemistry; vol. 41; (1949); p. 2788, View in Reaxys

-80 - 20

Goodeve; Transactions of the Faraday Society; vol. 30; (1934); p.

504; Chem. Zentralbl.; vol. 105; nb. II; (1934); p. 3228, View in Reaxys

NMR Spectroscopy (36) 1 of 36

Description (NMR Spec- Spectrum troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- [(2)H6]acetone scopy) Temperature (NMR Spectroscopy) [°C]

24.84

Frequency (NMR Spectroscopy) [MHz]

300

Location

supporting information

Kundrat, Ondrej; Eigner, Vaclav; Dvorakova, Hana; Lhotak, Pavel; Organic Letters; vol. 13; nb. 15; (2011); p.

4032 - 4035, View in Reaxys 2 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- formic acid; water scopy) Temperature (NMR Spectroscopy) [°C]

24

Frequency (NMR Spectroscopy) [MHz]

75.5

Chen, Ning; Xu, Jiaxi; Letters in Organic Chemistry; vol. 6; nb. 4; (2009); p. 349 - 353, View in Reaxys 3 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- dimethylsulfoxide-d6 scopy) Frequency (NMR Spectroscopy) [MHz]

400

Asghar, Basim H. M.; Crampton, Michael R.; Organic and Biomolecular Chemistry; vol. 5; nb. 10; (2007); p. 1646 - 1654, View in Reaxys 4 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Frequency (NMR Spectroscopy) [MHz]

60

Zarchi, Mohammad Ali Karimi; Zarei, Amin; Journal of the Chinese Chemical Society; vol. 52; nb. 2; (2005); p.

309 - 311, View in Reaxys

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5 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- acetone scopy) Temperature (NMR Spectroscopy) [°C]

35

Witanowski, Michal; Biedrzycka, Zenobia; Grela, Karol; Wejroch, Krystyna; Magnetic Resonance in Chemistry; vol. 36; nb. SPEC. ISS.; (1998); p. S85-S92, View in Reaxys 6 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- cyclohexane scopy) Temperature (NMR Spectroscopy) [°C]

35

Witanowski, Michal; Biedrzycka, Zenobia; Grela, Karol; Wejroch, Krystyna; Magnetic Resonance in Chemistry; vol. 36; nb. SPEC. ISS.; (1998); p. S85-S92, View in Reaxys 7 of 36

Nucleus (NMR Spectroscopy)

13C

Coupling Nuclei

13C

Solvents (NMR Spectro- CDCl3 scopy) Frequency (NMR Spectroscopy) [MHz]

125.76

Witanowski, Michal; Biedrzycka, Zenobia; Grela, Karol; Magnetic Resonance in Chemistry; vol. 36; nb. 5; (1998); p. 356 - 358, View in Reaxys 8 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Dailey; Shoolery; Journal of the American Chemical Society; vol. 77; (1955); p. 3977,3980, View in Reaxys; Meyer et al.; Journal of the American Chemical Society; vol. 75; (1953); p. 4567,4570, View in Reaxys; Boyle, Peter H.; Convery, Maire A.; Davis, Anthony P.; Hosken, Gladys D.; Murray, Brian A.; Journal of the Chemical Society, Chemical Communications; nb. 3; (1992); p. 239 - 242, View in Reaxys 9 of 36

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

1H-1H

Boyle, Peter H.; Convery, Maire A.; Davis, Anthony P.; Hosken, Gladys D.; Murray, Brian A.; Journal of the Chemical Society, Chemical Communications; nb. 3; (1992); p. 239 - 242, View in Reaxys 10 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

15N

Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance (1969-1992); vol. 97; nb. 3; (1992); p. 568 594, View in Reaxys

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11 of 36

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- benzene-d6 scopy) Temperature (NMR Spectroscopy) [°C]

23.9

Comment (NMR Spectroscopy)

13C-15N, 1H-15N.

Kupce, Eriks; Wrackmeyer, Bernd; Journal of Magnetic Resonance (1969-1992); vol. 97; nb. 3; (1992); p. 568 594, View in Reaxys 12 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) 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 13 of 36

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) 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 14 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- CDCl3 scopy) ITO, Haruko; ITO, Tasuku; Chemistry Letters; (1985); p. 1251 - 1254, View in Reaxys; Bailey, William F.; Cioffi, Eugene A.; Magnetic Resonance in Chemistry; vol. 25; (1987); p. 181 - 183, View in Reaxys 15 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) ITO, Haruko; ITO, Tasuku; Chemistry Letters; (1985); p. 1251 - 1254, View in Reaxys; Kurokawa; Anderson Jr.; Bulletin of the Chemical Society of Japan; vol. 58; nb. 1; (1985); p. 367 - 373, View in Reaxys 16 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Comeau, M.; Beraldin, M.-T.; Vauthier, E. C.; Fliszar, S.; Canadian Journal of Chemistry; vol. 63; (1985); p. 3226 3232, View in Reaxys

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17 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

1H

Solvents (NMR Spectro- CDCl3 scopy) 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 18 of 36

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) 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 19 of 36

Description (NMR Spec- Spin-spin coupling constants troscopy) Solvents (NMR Spectro- CDCl3 scopy) Comment (NMR Spectroscopy)

1H-1H

Kurokawa; Anderson Jr.; Bulletin of the Chemical Society of Japan; vol. 58; nb. 1; (1985); p. 367 - 373, View in Reaxys 20 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- acetone scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys 21 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- dimethylsulfoxide scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys 22 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- CCl4 scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys

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23 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

14N

Solvents (NMR Spectro- neat (no solvent) scopy) Witanowski, M.; Stefaniak, L.; Lamphun, B. Na; Webb, G. A.; Organic Magnetic Resonance; vol. 16; nb. 1; (1981); p. 57 - 59, View in Reaxys 24 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- ClSO2F scopy) Temperature (NMR Spectroscopy) [°C]

-60

Olah, George A.; Fung, Alexander P.; Rawdah, Tarik N.; Journal of Organic Chemistry; vol. 45; nb. 21; (1980); p.

4149 - 4153, View in Reaxys 25 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

Solvents (NMR Spectro- methanol; tetradeuteriomethanol scopy) Bowman, W. Russ; Golding, Bernard T.; Watson, William P.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1980); p. 731 - 736, View in Reaxys 26 of 36

Description (NMR Spec- NMR troscopy) Lippmaa,E.T. et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 924 - 928; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 1006 - 1011, View in Reaxys; Ejchart,A.; Organic Magnetic Resonance; vol. 10; (1977); p. 263, View in Reaxys; Englert; Zeitschrift fuer Elektrochemie; vol. 65; (1961); p. 854, View in Reaxys; Monitz; Gutowsky; Journal of Chemical Physics; vol. 38; (1963); p. 1155,1158, View in Reaxys; Ng; Organic Magnetic Resonance; vol. 2; (1970); p. 283, View in Reaxys; Bartuska; Maciel; Journal of Magnetic Resonance (1969-1992); vol. 5; (1971); p. 211, View in Reaxys; Cavanaugh; Dailey; Journal of Chemical Physics; vol. 34; (1961); p. 1099,1100, View in Reaxys; Nagy et al.; Bulletin des Societes Chimiques Belges; vol. 78; (1969); p. 639, View in Reaxys; Knunjanz et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1966); p. 1013; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; (1966); p. 1062, View in Reaxys; Miyazima et al.; Journal of Physical Chemistry; vol. 73; (1969); p. 1370, View in Reaxys; Hilbers et al.; Pure and Applied Chemistry; vol. 32; (1972); p. 197,199,202, View in Reaxys; Chertkov; Sergeev; Theoretical and Experimental Chemistry; vol. 10; (1974); p. 692; ; p. 837, View in Reaxys; Saito et al.; Canadian Journal of Chemistry; vol. 51; (1973); p. 2118,2121, View in Reaxys; Cheremisin; Schastnev; Journal of Structural Chemistry; vol. 19; (1978); p. 313; ; p. 364, 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; Zoltewicz; O'Halloran; Journal of Organic Chemistry; vol. 39; (1974); p. 89,90, View in Reaxys; Fetell; Feuer; Journal of Organic Chemistry; vol. 43; (1978); p. 1238,1241, View in Reaxys; Witanowski; Journal of the American Chemical Society; vol. 90; (1968); p. 5683, View in Reaxys; Olah; Kiovsky; Journal of the American Chemical Society; vol. 90; (1968); p. 6461, View in Reaxys; Alexandrou; Jannakoudakis; Tetrahedron Letters; (1968); p. 3841, View in Reaxys

27 of 36

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

NMR chemical shifts

Moniz; Poranski; jr.; Journal of Magnetic Resonance (1969-1992); vol. 11; (1973); p. 62, View in Reaxys 28 of 36

Description (NMR Spec- Spectrum troscopy)

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Witanowski et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 2569,2570, View in Reaxys; Sasaki; Suzuki; Chemical and Pharmaceutical Bulletin; vol. 17; (1969); p. 2049,2050, View in Reaxys; Hofman et al.; Journal of the American Chemical Society; vol. 86; (1964); p. 554,555, View in Reaxys 29 of 36

Description (NMR Spec- Chemical shifts troscopy) Sasaki et al.; Chemical and Pharmaceutical Bulletin; vol. 16; (1968); p. 2120, View in Reaxys

30 of 36

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

14N

Poranski; Moniz; Journal of Physical Chemistry; vol. 71; (1967); p. 1142, View in Reaxys 31 of 36

Description (NMR Spec- Spectrum troscopy) Comment (NMR Spectroscopy)

des nach γ-Bestr. bei 77 K erhaltenen Radikals

Chachaty; Comptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques; vol. 262; (1966); p. 680, View in Reaxys 32 of 36

Description (NMR Spec- Spin-spin coupling constants troscopy) Stone; Maki; Journal of Chemical Physics; vol. 37; (1962); p. 1326,1329, View in Reaxys; Deno et al.; Journal of Organic Chemistry; vol. 31; (1966); p. 1968, View in Reaxys

33 of 36

Description (NMR Spec- Chemical shifts troscopy) Comment (NMR Spectroscopy)

Verschieb. der 17O-NMR-Linien

Christ et al.; Helvetica Chimica Acta; vol. 44; (1961); p. 865, View in Reaxys 34 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

13C

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 35 of 36

Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)

17O

Weaver et al.; Journal of Chemical Physics; vol. 23; (1955); p. 1956, View in Reaxys 36 of 36

Description (NMR Spec- Spin-spin coupling constants troscopy) Comment (NMR Spectroscopy)

nucleus1-nucleus2:1H-1H.

Dailey; Shoolery; Journal of the American Chemical Society; vol. 77; (1955); p. 3977,3980, View in Reaxys IR Spectroscopy (20) 1 of 20

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

nematic phase

Comment (IR Spectroscopy)

1600 - 1300 cm**(-1)

Belhakem, M.; Jordanov, B.; Journal of Molecular Structure; vol. 218; (1990); p. 309 - 314, View in Reaxys 2 of 20

Description (IR Spectroscopy)

Polarization of IR bands

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Belhakem, M.; Jordanov, B.; Journal of Molecular Structure; vol. 218; (1990); p. 309 - 314, View in Reaxys 3 of 20

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

neat (no solvent)

Comment (IR Spectroscopy)

500 - 300 cm**(-1)

Beresneva, G. A.; Khristenko, L. V.; Ul'yanova, O. D.; Pentin, Yu. A.; Russian Journal of Physical Chemistry; vol.

60; nb. 4; (1986); p. 631 - 632; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 1045 - 1046, View in Reaxys 4 of 20

Description (IR Spectroscopy)

IR

Iogansen; Litovchenko; Journal of Applied Spectroscopy; vol. 2; (1965); p. 159; ; p. 243, View in Reaxys; Mauret et al.; Bulletin de la Societe Chimique de France; (1974); p. 379, View in Reaxys; Watarai et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 1448,1449, View in Reaxys; Geiseler; Kessler; Nitro Compounds., Proc. Intern. Symp.; (1964); p. 187 - 194; Chem.Abstr.; vol. 64; nb. 1928f; (1966), View in Reaxys; Fetell; Feuer; Journal of Organic Chemistry; vol. 43; (1978); p. 1238,1241, View in Reaxys; Groner et al.; Chemical Physics; vol.

11; (1975); p. 63,65,68,69-71,79, View in Reaxys 5 of 20

Description (IR Spectroscopy)

Spectrum

Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys; Buczkowski; Urbanski; Spectrochimica Acta; vol. 18; (1962); p. 1187,1188, View in Reaxys; Groner et al.; Chemical Physics; vol. 5; (1974); p. 136, View in Reaxys; Kinugasa; Watarai; Nippon Kagaku Zasshi; vol. 83; (1962); p. 472,474; Chem.Abstr.; vol.

58; nb. 13317e, View in Reaxys 6 of 20

Description (IR Spectroscopy)

Bands

Nowikow et al.; Tetrahedron, Supplement; vol. 6; (1964); p. 119,128; Chem.Abstr.; nb. 14665; (1965), View in Reaxys; Varsanyi et al.; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 23; (1967); p. 1205,1210, View in Reaxys 7 of 20

Description (IR Spectroscopy)

Intensity of IR bands

Kinugasa; Watarai; Nippon Kagaku Zasshi; vol. 83; (1962); p. 472,474; Chem.Abstr.; vol. 58; nb. 13317e, View in Reaxys; Popov; Shlyapochnikov; Optics and Spectroscopy; vol. 15; (1963); p. 174; ; p. 325, View in Reaxys 8 of 20

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

NO2-Streckschwingungsbanden; Druckabhaengigkeit (1610-9080 atm.).

Wiederkehr; Drickamer; Journal of Chemical Physics; vol. 28; (1958); p. 311,312, View in Reaxys 9 of 20

Description (IR Spectroscopy)

Spectrum

Solvent (IR Spectroscopy)

paraffin

Comment (IR Spectroscopy)

5000 - 1000 cm**(-1)

Urbanski; Roczniki Chemii; vol. 31; (1957); p. 37,45; Bulletin de l'Academie Polonaise des Sciences, Classe 3: Mathematique, Astronomie, Physique, Chimie, Geologie et Geographie; vol. 4; (1956); p. 381; Chem.Abstr.; (1957); p. 12659, View in Reaxys 10 of 20

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 667 cm**(-1); Dampf.

Pierson et al.; Analytical Chemistry; vol. 28; (1956); p. 1218,1222; A. P. I. Res. Project; vol. 44; nb. 1220; (1951), View in Reaxys 11 of 20

Description (IR Spectroscopy)

Spectrum

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Comment (IR Spectroscopy)

5000 - 455 cm**(-1); Fluessigkeit.

Smith et al; Journal of Chemical Physics; vol. 18; (1956); p. 706,708,709, View in Reaxys 12 of 20

Description (IR Spectroscopy)

Bands

Solvent (IR Spectroscopy)

CHCl3

Comment (IR Spectroscopy)

NO2-Streckschwingungsbanden.

Brown; Journal of the American Chemical Society; vol. 77; (1955); p. 6341,6344, View in Reaxys 13 of 20

Description (IR Spectroscopy)

Bands

Comment (IR Spectroscopy)

NO2-Streckschwingungsbanden der Fluessigkeit.

Haszeldine; Journal of the Chemical Society; (1953); p. 2525, View in Reaxys 14 of 20

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 455 cm**(-1); Dampf.

Smith et al.; Journal of Chemical Physics; vol. 18; (1950); p. 706,707,712, View in Reaxys 15 of 20

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 667 cm**(-1); der Fluessigkeit.

Nielsen; Smith; Industrial and Engineering Chemistry, Analytical Edition; vol. 15; (1943); p. 610, View in Reaxys 16 of 20

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

2000 - 800 cm**(-1); der Fluessigkeit.

Barnes; Liddel; Williams; Industrial and Engineering Chemistry, Analytical Edition; vol. 15; (1943); p. 659,687, View in Reaxys 17 of 20

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

10000 - 6250 cm**(-1); der Fluessigkeit.

Suhrmann; Klein; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 50; (1941); p. 50, View in Reaxys 18 of 20

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

1667 - 500 cm**(-1)

Mathieu; Massignon; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 212; (1941); p. 1085; Annales de Physique (Paris, France); vol. <11>16; (1941); p. 8,13, View in Reaxys 19 of 20

Description (IR Spectroscopy)

Spectrum

Comment (IR Spectroscopy)

5000 - 667 cm**(-1); Fluessigkeit.

A.P.I.Res.Project 44 Nr. 731<1948>,1752<1956>, View in Reaxys 20 of 20

Description (IR Spectroscopy)

Spectrum

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Comment (IR Spectroscopy)

10000 - 667 cm**(-1)

Coblentz,W.W.; Investigations of Infra-red Spectra <Washington 1905>,S.157,161,187, View in Reaxys Mass Spectrometry (9) Description (Mass Comment (Mass Spectrometry) Spectrometry)

References

Photoionization; TOFMS (Time of flight mass spectrum); Spectrum

Xie, Mingfeng; Zhou, Zhongyue; Wang, Zhandong; Chen, Dongna; Qi, Fei; International Journal of Mass Spectrometry; vol. 303; nb. 2-3; (2011); p. 137 - 146, View in Reaxys

spectrum; chemical ionization (CI)

Kadentsev; Kolotyrkina; Stomakhin; Chizhov; Shevelev; Russian Chemical Bulletin; vol. 46; nb. 6; (1997); p. 1184 - 1185, View in Reaxys

chemical ionization (CI)

Petris, Giulia De; Organic Mass Spectrometry; vol. 25; nb. 10; (1990); p. 557 - 558, View in Reaxys

fragmentation pattern; spectrum

Wodtke, A. M.; Hintsa, E. J.; Lee, Y. T.; Journal of Physical Chemistry; vol. 90; nb. 16; (1986); p. 3549 - 3558, View in Reaxys Large; Knof; Organic Mass Spectrometry; vol. 11; (1976); p. 582,593, View in Reaxys; Boschan; Smith; U.S.Dep.Comm.Off.Tech.Serv.Rep. 151120; (1957); Chem.Abstr.; nb.

10497; (1960), View in Reaxys; Fileleeva et al.; Theoretical and Experimental Chemistry; vol. 11; (1975); p. 283,285, View in Reaxys; Das; Koga; Suzuki; ; vol. 52; nb. 1; (1979); p. 65 - 68, View in Reaxys; Chizhov et al.; Organic Mass Spectrometry; vol. 13; (1978); p. 611,612, View in Reaxys; Tsuda et al.; Bulletin of the Chemical Society of Japan; vol.

42; (1969); p. 614, View in Reaxys; Fraser; Paul; Journal of the Chemical Society [Section] B: Physical Organic; (1968); p. 1407, View in Reaxys

negative ion spectroscopy

Large; Knof; Organic Mass Spectrometry; vol. 11; (1976); p. 582,593, View in Reaxys; Tsuda et al.; Bulletin of the Chemical Society of Japan; vol. 42; (1969); p. 614, View in Reaxys

ion-cyclotron resonance

Kriemler; Buttrill; Journal of the American Chemical Society; vol. 95; (1973); p. 1365, View in Reaxys

appearance potentials

Jaeger; Henglein; Zeitschrift fuer Naturforschung, Teil A: Astrophysik, Physik und Physikalische Chemie; vol. 22; (1967); p. 700, View in Reaxys Fragmentierung Collin; Bulletin de la Societe Royale des Sciences de Liege; vol. 23; (1954); p. 194 durch Elektronen- 196, View in Reaxys stoss

UV/VIS Spectroscopy (11) 1 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

methanol

Location

supporting information

Kopylovich, Maximilian N.; Mac Leod, Tatiana C. O.; Mahmudov, Kamran T.; Guedes Da Silva, M. Fatima C.; Pombeiro, Armando J. L.; Dalton Transactions; vol. 40; nb. 19; (2011); p. 5352 - 5361, View in Reaxys 2 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

water

Location

supporting information

Absorption Maxima (UV/ 272 VIS) [nm] Ext./Abs. Coefficient [l·mol-1cm-1]

17.7

Li, Zhao; Cheng, Jin-Pei; Parker, Vernon D.; Organic and Biomolecular Chemistry; vol. 9; nb. 12; (2011); p. 4563 4569, View in Reaxys 3 of 11

Description (UV/VIS Spectroscopy)

UV/VIS

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Barth et al.; Journal of the Chemical Society, Chemical Communications; (1975); p. 672, View in Reaxys; Bell, Cox; Journal of the Chemical Society [Section] B: Physical Organic; (1971); p. 783, View in Reaxys; Barth et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1979); p. 907,908, View in Reaxys; Belikov et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); vol. 20; (1971); p. 272,275; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; vol. 20; (1971); p. 335, View in Reaxys; Mayahi; Al-Baldawi; Journal of the Indian Chemical Society; vol. 48; (1971); p.

1171, View in Reaxys 4 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Ivanova,I.S. et al.; Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science (English Translation); (1968); p. 2038 - 2039; Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya; nb. 9; (1968); p. 2144 - 2146, View in Reaxys; Baly; Desch; Journal of the Chemical Society; vol. 93; (1908); p. 1750, View in Reaxys; Williams et al.; Journal of Organic Chemistry; vol. 30; (1965); p. 2674,2675, View in Reaxys; Ostaszynski et al.; Tetrahedron; vol. 25; (1969); p. 1929,1936, View in Reaxys 5 of 11

Description (UV/VIS Spectroscopy)

Absorption maxima

Bonnafous; Labarre; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 66; (1969); p. 1376, View in Reaxys; Bayliss; Wills-Johnson; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 551,553, View in Reaxys; Gast; Estes; Analytical Chemistry; vol. 32; (1960); p. 1712, View in Reaxys; Ungnade et al.; Journal of Physical Chemistry; vol. 68; (1964); p. 3226, View in Reaxys; Balasubramanian; Rao; Spectrochimica Acta; vol. 18; (1962); p. 1337; Chem.Abstr.; vol. 55; nb. 3419; (1961), View in Reaxys 6 of 11

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

ethanol

Urbanski; Ciecierska; Roczniki Chemii; vol. 29; (1955); p. 11,14,15; Chem.Abstr.; (1955); p. 11414, View in Reaxys; Urbanski; Tetrahedron; vol. 6; (1959); p. 1,5; Roczniki Chemii; vol. 33; (1959); p. 635,637, 638; Chem.Abstr.; (1960); p. 250, View in Reaxys 7 of 11

Description (UV/VIS Spectroscopy)

Absorption maxima

Solvent (UV/VIS Spectroscopy)

light petroleum

Haszeldine; Journal of the Chemical Society; (1953); p. 2525, View in Reaxys 8 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Comment (UV/VIS Spectroscopy)

des Dampfes.

Thompson; Pukis; Transactions of the Faraday Society; vol. 32; (1936); p. 678; Chem. Zentralbl.; vol. 108; nb. II; (1937); p. 955, View in Reaxys; Hirschlaff; Norrish; Journal of the Chemical Society; (1936); p. 1581, View in Reaxys; Goodeve; Transactions of the Faraday Society; vol. 30; (1934); p. 504; Chem. Zentralbl.; vol. 105; nb. II; (1934); p. 3228, View in Reaxys 9 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

ethanol

Hantzsch; Voigt; Chemische Berichte; vol. 45; (1912); p. 85,112; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 79; (1912); p. 597, View in Reaxys 10 of 11

Description (UV/VIS Spectroscopy)

Spectrum

Solvent (UV/VIS Spectroscopy)

aq. NaOH

Hantzsch; Voigt; Chemische Berichte; vol. 45; (1912); p. 85,112; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 79; (1912); p. 597, View in Reaxys 11 of 11

Description (UV/VIS Spectroscopy)

Spectrum

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Solvent (UV/VIS Spectroscopy)

ethanol

Comment (UV/VIS Spectroscopy)

neutrale und alkalische Loesungen.

Zelinski; Rosanow; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 78; (1912); p. 630, View in Reaxys; Hantzsch; Voigt; Zeitschrift fuer Physikalische Chemie, Stoechiometrie und Verwandtschaftslehre; vol. 79; (1912); p. 593, View in Reaxys ESR Spectroscopy (2) 1 of 2

Description (ESR Spectroscopy)

Spectrum

Tsuji et al.; Bulletin of the Chemical Society of Japan; vol. 43; (1970); p. 572, View in Reaxys; Trofimov; Chkheidze; High Energy Chemistry; vol. 1; (1967); p. 409, View in Reaxys; Morakinyo, Moshood K.; Chipinda, Itai; Hettick, Justin; Siegel, Paul D.; Abramson, Jonathan; Strongin, Robert; Martincigh, Bice S.; Simoyi, Reuben H.; Canadian Journal of Chemistry; vol. 90; nb. 9; (2012); p. 724 - 738, View in Reaxys 2 of 2

Description (ESR Spectroscopy)

ESR

Gilbert,B.C. et al.; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1972); p. 1272 - 1279, View in Reaxys; Gilbert; Treuwith; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1973); p. 2010,2013, View in Reaxys; Piette et al.; Journal of the American Chemical Society; vol. 84; (1962); p. 4212,4213, View in Reaxys; Chapelet-Letourneux et al.; Bulletin de la Societe Chimique de France; (1968); p. 3963, View in Reaxys Rotational Spectroscopy (1) Description (Rota- References tional Spectroscopy) Microwave spectrum

Ekkers et al.; Chemical Physics Letters; vol. 22; (1973); p. 249, View in Reaxys

Raman Spectroscopy (4) Description (Ram- Comment (Raman Spectroscopy) an Spectroscopy)

References

Spectrum

neat (no solvent)

Beresneva, G. A.; Khristenko, L. V.; Ul'yanova, O. D.; Pentin, Yu. A.; Russian Journal of Physical Chemistry; vol. 60; nb. 4; (1986); p. 631 - 632; Zhurnal Fizicheskoi Khimii; vol. 60; (1986); p. 1045 - 1046, View in Reaxys; Courtecuisse, Stephane; Cansell, Francois; Fabre, Denise; Petitet, Jean Pierre; Journal of Chemical Physics; vol. 108; nb. 17; (1998); p. 7350 - 7355, View in Reaxys

Bands

neat (no solvent)

Courtecuisse, Stephane; Cansell, Francois; Fabre, Denise; Petitet, Jean Pierre; Journal of Chemical Physics; vol. 108; nb. 17; (1998); p. 7350 - 7355, View in Reaxys

Spectrum

Spectrum

Mathieu; Massignon; Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences; vol. 212; (1941); p. 1085; Annales de Physique (Paris, France); vol. <11>16; (1941); p. 8,13, View in Reaxys; Wittek; Zeitschrift fuer Physikalische Chemie, Abteilung B: Chemie der Elementarprozesse, Aufbau der Materie; vol. 51; (1942); p.

188,197, View in Reaxys; Dadieu; Jele; Kohlrausch; Monatshefte fuer Chemie; vol. 58; (1931); p. 454, View in Reaxys; Geiseler; Kessler; Tetrahedron, Supplement; vol. 6; (1964); p. 187,188, View in Reaxys Fluessigkeit

Smith et al; Journal of Chemical Physics; vol. 18; (1956); p. 706,708,709, View in Reaxys

Luminescence Spectroscopy (1) Description (LuReferences minescence Spectroscopy) Sonoluminescence

Flint, Edward B.; Suslick, Kenneth S.; Journal of the American Chemical Society; vol. 111; nb. 18; (1989); p. 6987 - 6992, View in Reaxys

Fluorescence Spectroscopy (1) Description (Fluo- Comment (Fluorescence Specrescence Spectroscopy) troscopy) Spectrum

400 - 620 nm

References

Butler, L. J.; Krajnovich, D.; Lee, Y. T.; Ondrey, G.; Bersohn, R.; Journal of Chemical Physics; vol. 79; nb. 4; (1983); p. 1708 - 1722, View in Reaxys

Other Spectroscopic Methods (1)

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Description (Other Spectroscopic Methods)

References

Photoelectron spectrum

Mok, C. Y.; Kok, L. Y.; Chin, W. S.; Huang, H. H.; Journal of Molecular Structure; vol. 175; (1988); p. 429 434, View in Reaxys

Pharmacological Data (4) 1 of 4

Comment (Pharmacological Data)

Bioactivities present

Beilstein Handbook, View in Reaxys; Norris,R.K.; Randles,D.; Australian Journal of Chemistry; vol. 32; (1979); p.

1487 - 1509, View in Reaxys; Patent; ABBOTT LABORATORIES; EP371253; (1990); (A2) English, View in Reaxys; Troxler,F.; Helvetica Chimica Acta; vol. 51; (1968); p. 1214 - 1224, View in Reaxys; Lehr,F. et al.; Helvetica Chimica Acta; vol. 62; (1979); p. 2258 - 2275, View in Reaxys; Machacek,V. et al.; Collection of Czechoslovak Chemical Communications; vol. 33; (1968); p. 3579 - 3588, View in Reaxys; Hohenlohe-Oehringen,K.; Call,L.; Monatshefte fuer Chemie; vol. 99; nb. 4; (1968); p. 1313 - 1319, View in Reaxys; Patent; Merck and Co., Inc.; US3944560; (1976); (A1) English, View in Reaxys; Patent; Hennessy; Douglas J.; US3954793; (1976); (A1) English, View in Reaxys; Sakai; Oida; Oki; Chemical and pharmaceutical bulletin; vol. 16; nb. 6; (1968); p. 1048 - 1055, View in Reaxys; Kano; Komiyama; Takahagi; Shibuya; Chemical and Pharmaceutical Bulletin; vol. 24; nb. 4; (1976); p. 648 - 654, View in Reaxys; Patent; The Goodyear Tire and Rubber Company; US3989738; (1976); (A1) English, View in Reaxys; Takayama,H.; Okamoto,T.; Chemical and Pharmaceutical Bulletin; vol. 26; (1978); p.

2422 - 2427, View in Reaxys; Kaji; Harada; Zen; Chemical and Pharmaceutical Bulletin; vol. 26; nb. 10; (1978); p.

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2144, View in Reaxys; Gorbunov; Susarev; J. Appl. Chem. USSR (Engl. Transl.); vol. 41; (1968); p. 2680,2522, View in Reaxys; Liu; Ziegler; Journal of Chemical and Engineering Data; vol. 11; (1966); p. 187, View in Reaxys; Malone; Vining; Journal of Chemical and Engineering Data; vol. 12; (1967); p. 387, View in Reaxys; Watarai et al.; Bulletin of the Chemical Society of Japan; vol. 40; (1967); p. 1448,1449, View in Reaxys; Sutton; Dinh Son; Journal de Chimie Physique et de Physico-Chimie Biologique; vol. 64; (1967); p. 688, View in Reaxys; Su; Hong; Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy; vol. 24; (1968); p. 1461,1464, View in Reaxys; Weiss; Weiss; Angewandte Chemie; vol. 72; (1960); p. 413, View in Reaxys; Tur'jan; Tmekalowa; J. Appl. Chem.

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USSR (Engl. Transl.); vol. 37; (1964); p. 1776,1764, View in Reaxys; Spokes; Benson; Journal of the American Chemical Society; vol. 89; (1967); p. 6030,6034, View in Reaxys; Schwetlick et al.; Journal fuer Praktische Chemie (Leipzig); vol. 22; (1963); p. 113,119, View in Reaxys; Cann; Stirling; Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999); (1974); p. 817,818, 819, View in Reaxys; Saunders; Spaull; Zeitschrift fuer Physikalische Chemie (Muenchen, Germany); vol. 28; (1961); p. 332,337, View in Reaxys; Balasubramanian; Rao; Spectrochimica Acta; vol. 18; (1962); p. 1337; Chem.Abstr.; vol. 55; nb. 3419; (1961), View in Reaxys; Tolstova et al.; J. Appl. Chem. USSR (Engl. Transl.); vol. 43; (1970); p. 1305,1310,1311,1312, View in Reaxys; Bartmess et al.; Journal of the American Chemical Society; vol. 101; (1979); p. 6046,6049,6053, View in Reaxys; Zboinski et al.; Chemical Physics; vol. 40; (1979); p. 77,83, View in Reaxys; Belyaev; Prokopovich; Zhurnal Organicheskoi Khimii; vol. 7; (1971); p. 1599,1661, View in Reaxys; Barnard et al.; Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry (1972-1999); (1976); p. 961,964, View in Reaxys; Hilbers et al.; Pure and Applied Chemistry; vol. 32; (1972); p. 197,199,202, View in Reaxys; Reid; Tucker; Journal of the Chemical Society [Section] D: Chemical Communications; (1970); p. 1286, View in Reaxys; Chertkov; Sergeev; Theoretical and Experimental Chemistry; vol. 10; (1974); p. 692; ; p. 837, View in Reaxys; Petrula et al.; Journal of Chemical Physics; vol. 68; (1978); p. 623, View in Reaxys; Watanabe et al.; Journal of Quantitative Spectroscopy

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21; (1985); p. 1635 - 1638; Zhurnal Organicheskoi Khimii; vol. 21; nb. 8; (1985); p. 1790 - 1794, View in Reaxys; Bergbreiter, David E.; Lalonde, James J.; Journal of Organic Chemistry; vol. 52; nb. 8; (1987); p. 1601 - 1603, View in Reaxys; Olah, George A.; Rochin, Christophe; Journal of Organic Chemistry; vol. 52; nb. 4; (1987); p. 701 - 702, View in Reaxys; Koft, Emil R.; Journal of Organic Chemistry; vol. 52; nb. 15; (1987); p. 3466 - 3468, View in Reaxys; Olsson, Thomas; Stern, Kaye; Journal of Organic Chemistry; vol. 53; nb. 11; (1988); p. 2468 2472, View in Reaxys; Mancera, Manuel; Rodriguez, Enrique; Roffe, Isaac; Galbis, Juan A.; Journal of Organic Chemistry; vol. 53; nb. 24; (1988); p. 5648 - 5651, View in Reaxys; Hauser, Frank M.; Baghdanov, Vaceli M.; Journal of Organic Chemistry; vol. 53; nb. 20; (1988); p. 4676 - 4681, View in Reaxys; Ros, Francisco; Rosa, Jose de la; Journal of Organic Chemistry; vol. 53; nb. 12; (1988); p. 2868 - 2870, View in Reaxys; Ballini, Roberto; Petrini, Marino; Marcantoni, Enrico; Rosini, Goffredo; Synthesis; nb. 3; (1988); p. 231 - 233, View in Reaxys; Melot, Jean-Marie; Texier-Boullet, Francoise; Foucaud, Andre; Synthesis; nb. 4; (1987); p. 364 - 366, View in Reaxys; Ono, Noboru; Fujii, Masayuki; Kaji, Aritsune; Synthesis; nb. 6; (1987); p. 532 - 535, View in Reaxys; Kandil, Ali A.; Porter, Terence M.; Slessor, Keith N.; Synthesis; nb. 4; (1987); p. 411 - 413, View in Reaxys; Flint, Edward B.; Suslick, Kenneth S.; Journal of the American Chemical Society; vol. 111; nb. 18; (1989); p. 6987 - 6992, View in Reaxys; Node, Manabu; Nagasawa, Hideko; Naniwa, Yoshimitsu; Fuji, Kaoru; Synthesis; nb. 8; (1987);

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71; nb. 40; (2015); p. 7575 - 7582; Art.No: 27027, View in Reaxys; Choudhary, Manoj K.; Tak, Rajkumar; Kureshy, Rukhsana I.; Ansari, Amamudin; Khan, Noor-Ul H.; Abdi, Sayed H.R.; Bajaj, Hari C.; Journal of Molecular Catalysis A: Chemical; vol. 409; (2015); p. 85 - 93; Art.No: 9596, View in Reaxys; Angulo, Beatriz; Garca, Jos I.; Herreras, Clara I.; Mayoral, Jos A.; Miana, Ana C.; Organic and Biomolecular Chemistry; vol. 13; nb. 35; (2015); p. 9314 - 9322, View in Reaxys; Aksenov, Nicolai A.; Aksenov, Alexander V.; Nadein, Oleg N.; Aksenov, Dmitrii A.; Smirnov, Alexander N.; Rubin, Michael; RSC Advances; vol. 5; nb. 88; (2015); p. 71620 - 71626, View in Reaxys; Abdelli, Abderrahmen; Efrit, Mohamed Lotfi; Gaucher, Anne; M'rabet, Hedi; Prim, Damien; Tetrahedron Letters; vol. 56; nb. 40; (2015); p. 5397 - 5400, View in Reaxys; Ren, Ren; Ma, Jiantai; RSC Advances; vol. 5; nb. 91; (2015); p. 74802 - 74810, View in Reaxys; Patent; QUADRIGA BIOSCIENCES, INC.; JANDELEIT, BERND; FISCHER, WOLF-NICOLAS; KOLLER, KERRY J.; US2015/218085; (2015); (A1) English, View in Reaxys; Patent; F. HOFFMANN-LA ROCHE AG; 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; WO2015/113990; (2015); (A1) English, View in Reaxys; Yu, Lei; Zhang, Qi; Li, Shu-Shuang; Huang, Jun; Liu, Yong-Mei; He, He-Yong; Cao, Yong; ChemSusChem; vol.

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Effect (Pharmacological Data)

pharmacokinetics

Species or Test-System (Pharmacological Data)

nitroalkane oxidase of Streptomyces ansochromogenes

Type (Pharmacological Data)

Km

Value of Type (Pharmacological Data)

26.8 mmol/l

Li, Yanhua; Gao, Zengqiang; Hou, Haifeng; Li, Lei; Zhang, Jihui; Yang, Haihua; Dong, Yuhui; Tan, Huarong; Biochemical and Biophysical Research Communications; vol. 405; nb. 3; (2011); p. 344 - 348, View in Reaxys 3 of 4

Effect (Pharmacological Data)

binding affinity

Species or Test-System (Pharmacological Data)

recombinant nitronate monooxygenase of Hansenula mrakii

Kind of Dosing (Pharmacological Data)

title comp. administered as nitronate form dissolved in ethanol

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Further Details (Pharmacological Data)

dissociation constant (Kd)

Type (Pharmacological Data)

Kd

Value of Type (Pharmacological Data)

5.9 mmol/l

Francis, Kevin; Gadda, Giovanni; Bioorganic Chemistry; vol. 37; nb. 5; (2009); p. 167 - 172, View in Reaxys 4 of 4

Effect (Pharmacological Data)

binding affinity

Species or Test-System (Pharmacological Data)

recombinant nitronate monooxygenase of Hansenula mrakii

Kind of Dosing (Pharmacological Data)

title comp. administered as nitronate form dissolved in ethanol

Results

molecular target: nitronate monooxygenase

Francis, Kevin; Gadda, Giovanni; Bioorganic Chemistry; vol. 37; nb. 5; (2009); p. 167 - 172, View in Reaxys Transport and Distribution (4) 1 of 4

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 2.39E3 - 3.36E3 l/kgHA; relative humidity affected experimental partition coefficient by up to a factor of 3

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated at least 48 h; <0.01 percent-98 percent relative humidity; 15 deg C; relative humidity effect on partition equilibrium

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 2 of 4

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

air - Leonardite humic acid

Results

experimental sorption enthalpy, ΔabsHi = -38.8 kJ/mol

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5 to 75 deg C

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 3 of 4

Type (Transport and Distribution)

partition

Media (Transport and Distribution)

air - Leonardite humic acid

Results

Leonardite humic acid/air partition coefficient, KHA,air = 4.20E2 - 2.85E3 l/kgHA; no glass transitions below 75 deg C that had an effect on the sorption properties of humic acid as indicated by linear van't Hoff plot

Method, Remarks (Transport and Distribution)

dynamic flow-through technique; IGC-FID; title comp. injected onto the column packed with humic acid (<2 μm thick) coated glass beads; equilibrated for 80 d; 98 percent relative humidity; 5-75 deg C; temperature dependence of partition equilibrium studied

Niederer, Christian; Goss, Kai-Uwe; Schwarzenbach, Rene P.; Environmental Science and Technology; vol. 40; nb. 17; (2006); p. 5368 - 5373, View in Reaxys 4 of 4

Type (Transport and Distribution)

sorption

Media (Transport and Distribution)

vapour-soil

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Results

capacity and solubility of liquid in peat organic matter (from the vapour isotherm): partition capacity (Q0 om): 272 mg/g, volume fraction solubility (Φ0): 0.25; vapour sorption isotherm

Method, Remarks (Transport and Distribution)

static chamber; peat: organic content: 86.4 percent (dry weight), BET-(N2) surface area: 1.3-1.5 m2/g; 24 deg C

Chiou; Kile; Environmental Science and Technology; vol. 28; nb. 6; (1994); p. 1139 - 1144, View in Reaxys Oxygen Demand (1) 1 of 1

Type (Oxygen Demand)

COD/ThOD

Related to

Substance

Ratio BOD5/COD

0.63

Method, Remarks (Oxygen Demand)

ThOD: theoretical oxygen demand; COD determined according to Standard Methods (1976) using MilliQ water and potassium dichromate; ThOD is the stoichiometric amount of oxygen required to oxidize a compound to end product

Baker, James R.; Milke, Mark W.; Mihelcic, James R.; Water Research; vol. 33; nb. 2; (1999); p. 327 - 334, View in Reaxys Use (5) Use Pattern

References

distillation aid for separating crude chlorosilane streams of lowerboiling chlorosilanes and higherboiling chlorosilanes

Patent; DOW CORNING CORPORATION; WO2007/67723; (2007); (A1) English, View in Reaxys

Polar aprotic solvent for preparation of silane esters

Patent; Xerox Corporation; US2006/122414; (2006); (A1) English, View in Reaxys; Patent; Xerox Corporation; EP1669362; (2006); (A1) English, View in Reaxys

stabilizer for 1 bromopropane

Patent; ALBEMARLE CORPORATION; WO2006/119213; (2006); (A2) English, View in Reaxys

Anhydrous aprotic Patent; Gong, Chen; US2006/3963; (2006); (A1) English, View in Reaxys solvent for the reaction of hydroxygroup protection Dichloromethane stabilizer

Patent; SHOWA DENKO K.K.; WO2005/102970; (2005); (A1) English, View in Reaxys

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