Acetic acid (10R,13S,14R,17R)-14-hydroxy-17-(2-hydroxy-acetyl)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester | 104806-61-3

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: Acetic acid (10R,13S,14R,17R)-14-hydroxy-17-(2-hydroxy-acetyl)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester
• CAS: 104806-61-3
• 化学式: C₂₃H₃₂O₆
• 分子量: 404.503
• InChiKey: KWWMPZHEWVPAGP-HHNNQCTQSA-N

物化性质

• 沸点：
  555.0±50.0 °C(Predicted)
• 密度：
  1.27±0.1 g/cm3(Predicted)

反应信息

• 作为反应物：
  描述：

  乙酸酐 、 Acetic acid (10R,13S,14R,17R)-14-hydroxy-17-(2-hydroxy-acetyl)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester 以 溶剂黄146 为溶剂， 生成 Acetic acid (10R,13S,14R,17R)-17-(2-acetoxy-acetyl)-14-hydroxy-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester
  参考文献：
  名称：

  Investigation of the dependence of the direction of microbiological hydroxylation on the structure of substituted pregnanes

  摘要：

  DOI：

  10.1007/bf00776339
• 作为产物：
  描述：

  17α-acetate of cortexolone 以 水 、 N,N-二甲基甲酰胺 为溶剂， 生成 Hydrocortison-17-acetat 、 Acetic acid (10R,13S,14R,17R)-14-hydroxy-17-(2-hydroxy-acetyl)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester 、 Acetic acid (6S,10R,11S,13S,14R,17R)-6,11,14-trihydroxy-17-(2-hydroxy-acetyl)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester
  参考文献：
  名称：

  Investigation of the dependence of the direction of microbiological hydroxylation on the structure of substituted pregnanes

  摘要：

  DOI：

  10.1007/bf00776339