α,α-二甲基色胺
| α,α-二甲基色胺 | |
|---|---|
| |
| 识别 | |
| CAS号 | 304-53-0 
|
| 性质 | |
| 化学式 | C12H16N2 |
| 摩尔质量 | 188.27 g·mol−1 |
| 熔点 | 122—126 °C（395—399 K）[1] |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
α,α-二甲基色胺是一种有机化合物，化学式为C12H16N2，它是二甲基色胺的同分异构体之一。它可由3-(2-甲基-2-硝基丙基)-1H-吲哚在催化下由氢气[2]或水合肼[3]还原制得。它和1-(2,6-二甲基苯氧基)-2,3-环氧丙烷反应，可以得到1-(2,6-二甲基苯氧基)-3-[(2-(1H-吲哚-3-基)-1,1-二甲基乙基)氨基]2-丙醇[1]。
参考文献
- ^ 1.0 1.1 Kreighbaum, William E.; Matier, W. Lesley; Dennis, Ronald D.; Minielli, Joseph L.; Deitchman, David; Perhach, James L.; Comer, William T. Antihypertensive indole derivatives of phenoxypropanolamines with .beta.-adrenergic receptor antagonist and vasodilating activity. Journal of Medicinal Chemistry. 1980-03, 23 (3): 285–289. ISSN 0022-2623. doi:10.1021/jm00177a015 （英语）.
- ^ Shyam, Radhe; Nauton, Lionel; Angelici, Gaetano; Roy, Olivier; Taillefumier, Claude; Faure, Sophie. NC α‐ gem ‐dimethylated peptoid side chains: A novel approach for structural control and peptide sequence mimetics. Biopolymers. 2019-06, 110 (6) [2022-03-23]. ISSN 0006-3525. doi:10.1002/bip.23273. （原始内容存档于2022-03-23） （英语）.
- ^ Yeung, Bryan K. S.; Zou, Bin; Rottmann, Matthias; Lakshminarayana, Suresh B.; Ang, Shi Hua; Leong, Seh Yong; Tan, Jocelyn; Wong, Josephine; Keller-Maerki, Sonja. Spirotetrahydro β-Carbolines (Spiroindolones): A New Class of Potent and Orally Efficacious Compounds for the Treatment of Malaria. Journal of Medicinal Chemistry. 2010-07-22, 53 (14): 5155–5164 [2022-03-23]. ISSN 0022-2623. PMC 6996867
. PMID 20568778. doi:10.1021/jm100410f. （原始内容存档于2020-04-19） （英语）.
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