(2S,6S)-7-Methoxy-2-((3S,8S,9S,10R,13S,14S,17R)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methyl-heptan-3-one | 64142-16-1

• 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: (2S,6S)-7-Methoxy-2-((3S,8S,9S,10R,13S,14S,17R)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methyl-heptan-3-one
• CAS: 64142-16-1
• 化学式: C₂₉H₄₈O₃
• 分子量: 444.698
• InChiKey: ZMFIUSNLRSBBQI-IRUBHIRZSA-N

物化性质

• 沸点：
  534.5±35.0 °C(Predicted)
• 密度：
  1.02±0.1 g/cm3(Predicted)

反应信息

• 作为反应物：
  描述：

  (2S,6S)-7-Methoxy-2-((3S,8S,9S,10R,13S,14S,17R)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methyl-heptan-3-one 在 吡啶 、 sodium tetrahydroborate 作用下， 以 乙醇 为溶剂， 生成 2-Nitro-benzoic acid (1R,4S)-5-methoxy-1-[(S)-1-((3S,8S,9S,10R,13S,14S,17R)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-ethyl]-4-methyl-pentyl ester
  参考文献：
  名称：

  Dormantinol, a possible precursor in solanidine biosynthesis, from budding Veratrum grandiflorum

  摘要：

  DOI：

  10.1016/s0031-9422(00)94367-x
• 作为产物：
  描述：

  (2S,6S)-7-Hydroxy-2-((3S,8S,9S,10R,13S,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methyl-heptan-3-one 、 碘甲烷 在 silver(l) oxide 作用下， 以 二氯甲烷 为溶剂， 生成 (2S,6S)-7-Methoxy-2-((3S,8S,9S,10R,13S,14S,17R)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methyl-heptan-3-one
  参考文献：
  名称：

  Dormantinol, a possible precursor in solanidine biosynthesis, from budding Veratrum grandiflorum

  摘要：

  DOI：

  10.1016/s0031-9422(00)94367-x