N-甲基豬毛菜酚
N-甲基豬毛菜酚 | |
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識別 | |
CAS號 | 53622-85-8 |
PubChem | 124148 |
SMILES |
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ChEBI | 88540 |
性質 | |
化學式 | C11H15NO2 |
摩爾質量 | 193.24 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
N-甲基豬毛菜酚(英語:N-Methylsalsolinol)是一種有機化合物,化學式為C11H15NO2,具有很強的神經毒性[1]。它可由脫氧腎上腺素和乙醛在催化下反應製得[2]。它存在R和S異構體,其異構體可以通過高效液相色譜法進行分離[3]。
參考文獻
- ^ 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.