環戊胺
| 環戊胺 | |
|---|---|
| |
| 別名 | 氨基環戊烷 環戊基胺 |
| 識別 | |
| CAS號 | 1003-03-8 
|
| PubChem | 2906 |
| 性質 | |
| 化學式 | C5H11N |
| 摩爾質量 | 85.15 g·mol−1 |
| 密度 | 0.8512 g·cm−3（25 °C）[1] |
| 熔點 | −82.7 °C（190.5 K）[2] |
| 沸點 | 108 °C（381 K）[2] |
| 相關物質 | |
| 相關化學品 | 環丁胺 環己胺 |
| 若非註明，所有數據均出自標準狀態（25 ℃，100 kPa）下。 | |
環戊胺是一種有機化合物，化學式為C5H11N。它可由硝基環戊烷的還原反應[3]或環戊酮的還原胺化反應[4]製得。在碳酸鉀存在下，它和溴乙酰溴反應，可以得到N-環戊基溴乙酰胺。[5]
參考文獻
- ^ Frederick W. Bollinger, F. N. Hayes, Samuel Siegel. The Base-Catalyzed Decomposition of N-Nitroso-N-cyclopentylurethan 1. Journal of the American Chemical Society. 1953-04, 75 (7): 1729–1730 [2021-12-10]. ISSN 0002-7863. doi:10.1021/ja01103a503 （英語）.
- ^ 2.0 2.1 "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2021-12-05].
- ^ Felix Unglaube, Carsten Robert Kreyenschulte, Esteban Mejía. Development and Application of Efficient Ag‐based Hydrogenation Catalysts Prepared from Rice Husk Waste. ChemCatChem. 2021-06-08, 13 (11): 2583–2591 [2021-12-10]. ISSN 1867-3880. doi:10.1002/cctc.202100045 （英語）.
- ^ Jia Zhang, Jian Yang, Junying Tian, Hailong Liu, Xuemei Li, Weiguo Fang, Xun Hu, Chungu Xia, Jing Chen, Zhiwei Huang. Reductive amination of bio-based 2-hydroxytetrahydropyran to 5-Amino-1-pentanol over nano-Ni–Al 2 O 3 catalysts. New Journal of Chemistry. 2021, 45 (9): 4236–4245 [2021-12-10]. ISSN 1144-0546. doi:10.1039/D0NJ04962J （英語）.
- ^ D. S. S. M. Uppu, M. Bhowmik, S. Samaddar, J. Haldar. Cyclization and unsaturation rather than isomerisation of side chains govern the selective antibacterial activity of cationic-amphiphilic polymers. Chemical Communications. 2016, 52 (25): 4644–4647 [2021-12-10]. ISSN 1359-7345. doi:10.1039/C5CC09930G （英語）.