5-二乙氨基戊醇
| 5-二乙氨基戊醇 | |
|---|---|
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| 识别 | |
| CAS号 | 2683-57-0 
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| SMILES |
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| 性质 | |
| 化学式 | C9H21NO |
| 摩尔质量 | 159.27 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
5-二乙氨基戊醇是一种有机化合物，化学式为C9H21NO。它可由1,5-戊二醇和二乙胺为原料反应得到。[1]它可以在5-二乙氨基-5-氧代戊酸甲酯和氢化铝锂的还原反应中生成。[2]它和碘乙烷反应，可以得到羟戊基三乙基碘化铵。[3]
参考文献[编辑]
- ^ Sun, Weimin; Luo, Juntao; Huang, Wenqiang; Zhu, Xiaoxia. Application of the sulfonate ester group as a linker for solid phase organic synthesis. Chinese Journal of Reactive Polymers, 2001. 10 (1): 21-26. ISSN 1004-7646.
- ^ Analogs of 8-[[6-(diethylamino)hexyl]amino]-6-methoxy-4-methylquinoline as candidate antileishmanial agents. Journal of Medicinal Chemistry (1980), 23 (9), 981-985. doi:10.1021/jm00183a004.
- ^ Barbry, Didier; Hasiak, Bruno. Study of interactions between alcohol and amine functions. Thermolysis of hydroxides and salts of ω-(trialkylammonio)-1-alkanols（法文）. Collection of Czechoslovak Chemical Communications, 1983. 48 (6): 1734-1744. ISSN 0366-547X.