环丙胺
| 环丙胺 | |
|---|---|
| |
| 别名 | cyclopropylamine |
| 识别 | |
| CAS号 | 765-30-0 
|
| PubChem | 69828 |
| 性质 | |
| 化学式 | C3H7N |
| 摩尔质量 | 57.09 g·mol−1 |
| 外观 | 无色液体 |
| 熔点 | -35.4 °C（238 K） |
| 沸点 | 49-50 °C |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
环丙胺是一种有机化合物，化学式为C
3H
5NH
2。它可由硝基环丙烷催化加氢还原制得。[1]
反应
[编辑]环丙胺和苯甲醛在甲醇中反应，可以得到N-亚苄基环丙胺。[2]
它和二碳酸二叔丁酯反应，可以得到N-环丙基氨基甲酸叔丁酯。[3]
参考文献
[编辑]- ^ Dandu Damodara; et al. Polymethylhydrosiloxane derived palladium nanoparticles for chemo- and regioselective hydrogenation of aliphatic and aromatic nitro compounds in water. RSC Adv., 2014, 4, 22567-22574. doi:10.1039/C4RA01333F.
- ^ Sathiyaraj, Ethiraj; et al. Effect of N-Bound Organic Moiety in Dithiocarbamate (R2NCS-2) and trans Influence of Triphenylphosphine on NiS2PN Chromophore. Phosphorus, Sulfur and Silicon and the Related Elements (2015), 190 (7), 1127-1137. doi:10.1080/10426507.2014.976337.
- ^ Tars, Kaspars; et al. Targeting Carnitine Biosynthesis: Discovery of New Inhibitors against γ-Butyrobetaine Hydroxylase. Journal of Medicinal Chemistry (2014), 57 (6), 2213-2236. doi:10.1021/jm401603e.