3-乙硫基丙腈
外观
3-乙硫基丙腈 | |
---|---|
别名 | 乙基(氰乙基)硫醚 |
识别 | |
CAS号 | 3088-46-8 |
性质 | |
化学式 | C5H9NS |
摩尔质量 | 115.2 g·mol−1 |
熔点 | 49 °C(322 K)[1] |
沸点 | 105—109 °C(378—382 K)(30 torr)[2] |
相关物质 | |
相关化学品 | 3-巯基丙腈 3-甲硫基丙腈 |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
3-乙硫基丙腈是一种有机化合物,化学式为C5H9NS,它可由丙烯腈和乙硫醇在甲醇钠存在下反应得到。[2]它和氨基硫脲加热反应,可以得到5-(2-乙硫基乙基)-1,3,4-噻二唑-2-胺。[3]它可以被氢化铝锂还原为3-乙硫基丙胺。[2]
参考文献
[编辑]- ^ Butskus, P. F.; Denis, G. I. Cyanoethylation of aromatic amines by acrylonitrile and β-substituted propionitriles. Nauchnye Doklady Vysshei Shkoly, Khimiya i Khimicheskaya Tekhnologiya, 1958: 743-745. ISSN 0470-469X. CODEN NDVSAJ.
- ^ 2.0 2.1 2.2 Richard Göschke, Stefan Stutz, Vittorio Rasetti, Nissim-Claude Cohen, Joseph Rahuel, Pascal Rigollier, Hans-Peter Baum, Peter Forgiarini, Christian R. Schnell, Trixie Wagner, Markus G. Gruetter, Walter Fuhrer, Walter Schilling, Frédéric Cumin, Jeanette M. Wood, Jürgen Maibaum. Novel 2,7-Dialkyl-Substituted 5( S )-Amino-4( S )-hydroxy-8-phenyl-octanecarboxamide Transition State Peptidomimetics Are Potent and Orally Active Inhibitors of Human Renin. Journal of Medicinal Chemistry. 2007-10-01, 50 (20): 4818–4831 [2022-07-26]. ISSN 0022-2623. doi:10.1021/jm070314y. (原始内容存档于2022-07-26) (英语).
- ^ M. A. Kukaniev, M. D. Osimov, Z. G. Sangov, S. S. Safarov, M. B. Karimov, T. R. Radjabov. Polyfunctional nitriles in the synthesis of derivatives of 1,3,4-thiadiazolo-[3,2-a]pyrimidines. Chemistry of Heterocyclic Compounds. 2008-07, 44 (7): 882–885 [2022-07-26]. ISSN 0009-3122. doi:10.1007/s10593-008-0125-2 (英语).