3-乙酰氧基吗啡
外观
(重定向自3-乙酰基羟吗啡酮)
| 3-乙酰氧基吗啡 | |
|---|---|
| 首选IUPAC名 14-Hydroxy-17-methyl-6-oxo-4,5α-epoxymorphinan-3-yl acetate | |
| 系统IUPAC名 (4R,4aS,7aR,12bS)-4a-Hydroxy-3-methyl-7-oxo-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methano[1]benzofuro[3,2-e]isoquinolin-9-yl acetate | |
| 别名 | Oxymorphone acetate |
| 识别 | |
| CAS号 | 75660-23-0 |
| PubChem | 10860829 |
| ChemSpider | 9036119 |
| SMILES |
|
| InChI |
|
| InChIKey | DMGAPZQHWZFIRE-GRGSLBFTSA-N |
| 性质 | |
| 化学式 | C19H21NO5 |
| 摩尔质量 | 343.37 g·mol−1 |
| 若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 | |
3-乙酰氧基吗啡(英語:3-Acetyloxymorphone,称为或羟吗啡酮乙酸酯,Oxymorphone acetate)是一种含氮有机化合物,化学式C
19H
21NO
5,属于羟吗啡酮的乙酰基衍生物,能用作類阿片镇痛药[1]。
参考文献
[编辑]- ^ Werner, Lukas; Wernerova, Martina; Machara, Ales; Endoma-Arias, Mary Ann; Duchek, Jan; Adams, David R.; Cox, D. Phillip; Hudlicky, Tomas. UnexpectedN-Demethylation of Oxymorphone and OxycodoneN-Oxides Mediated by the Burgess Reagent: Direct Synthesis of Naltrexone, Naloxone, and Other Antagonists from Oxymorphone. Advanced Synthesis & Catalysis. 2012, 354 (14–15): 2706–2712. doi:10.1002/adsc.201200676.