N-甲基猪毛菜酚
| N-甲基猪毛菜酚 | |
|---|---|
-N-Methylsalsolinol.svg)
| |
| 识别 | |
| CAS号 | 53622-85-8 
|
| PubChem | 124148 |
| SMILES |
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| ChEBI | 88540 |
| 性质 | |
| 化学式 | C11H15NO2 |
| 摩尔质量 | 193.24 g·mol−1 |
| 若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。 | |
N-甲基猪毛菜酚（英語：N-Methylsalsolinol）是一种有机化合物，化学式为C11H15NO2，具有很强的神经毒性[1]。它可由脱氧肾上腺素和乙醛在催化下反应制得[2]。它存在R和S异构体，其异构体可以通过高效液相色谱法进行分离[3]。
参考文献
- ^ Quan, Zhe; Song, Yaru; Peters, Gladys; Shenwu, Ming; Sheng, Yinghong; Hwang, Huey-Min; Liu, Yi-Ming. Chiral CE Separation of Dopamine-Derived Neurotoxins. Analytical Sciences. 2005-02, 21 (2): 115–119. doi:10.2116/analsci.21.115.
- ^ Ohla, Stefan; Beyreiss, Reinhild; Fritzsche, Stefanie; Glaser, Petra; Nagl, Stefan; Stockhausen, Kai; Schneider, Christoph; Belder, Detlev. Monitoring On‐Chip Pictet–Spengler Reactions by Integrated Analytical Separation and Label‐Free Time‐Resolved Fluorescence. Chemistry – A European Journal. 2012-01-23, 18 (4): 1240–1246. doi:10.1002/chem.201101768.
- ^ Deng, Yulin; Maruyama, Wakako; Dostert, Philippe; Takahashi, Tsutomu; Kawai, Masao; Naoi, Makoto. Determination of the (R)- and (S)-enantiomers of salsolinol and N-methylsalsolinol by use of a chiral high-performance liquid chromatographic column. Journal of Chromatography B: Biomedical Sciences and Applications. 1995-08, 670 (1): 47–54. doi:10.1016/0378-4347(95)00136-7.