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环戊胺

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环戊胺
别名 氨基环戊烷
环戊基胺
识别
CAS号 1003-03-8  checkY
PubChem 2906
性质
化学式 C5H11N
摩尔质量 85.15 g·mol−1
密度 0.8512 g·cm−3(25 °C)[1]
熔点 −82.7 °C(190.5 K)[2]
沸点 108 °C(381 K)[2]
相关物质
相关化学品 环丁胺
环己胺
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

环戊胺是一种有机化合物,化学式为C5H11N。它可由硝基环戊烷的还原反应[3]环戊酮的还原胺化反应[4]制得。在碳酸钾存在下,它和溴乙酰溴反应,可以得到N-环戊基溴乙酰胺。[5]

参考文献

  1. ^ 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 (英语). 
  2. ^ 2.0 2.1 "PhysProp" data were obtained from Syracuse Research Corporation of Syracuse, New York (US). Retrieved from SciFinder. [2021-12-05].
  3. ^ 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 (英语). 
  4. ^ 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 (英语). 
  5. ^ 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 (英语).