9,10-di-tert-butyldimethylsilyloxystearic acid ethyl ester | 1131964-76-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 9,10-di-tert-butyldimethylsilyloxystearic acid ethyl ester
• CAS: 1131964-76-5
• 化学式: C₃₂H₆₈O₄Si₂
• 分子量: 573.061
• InChiKey: QXSBGKAZOJTOBW-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.81
• 重原子数：
  38.0
• 可旋转键数：
  21.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.97
• 拓扑面积：
  44.76
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  9,10-di-tert-butyldimethylsilyloxystearic acid ethyl ester 在 barium dihydroxide 作用下， 以 甲醇 为溶剂， 反应 2.0h， 以1.136 g的产率得到9,10-di-tert-butyldimethylsilyloxystearic acid
  参考文献：
  名称：

  Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters

  摘要：

  Several efficient synthetic routes giving readily access to (oxy)-sitosterol esters and (oxy)cholesterol esters derived respectively from oleic acid and from 9,10-dihydroxystearic acid were developed for the first time. This approach allowed that sufficient amounts of the latter were available in order to carry out further biological studies. (c) 2008 Elsevier Inc. All rights reserved.

  DOI：

  10.1016/j.steroids.2008.04.010
• 作为产物：
  描述：

  9,10-dihydroxystearic acid ethyl ester 、 叔丁基二甲基氯硅烷 在 咪唑 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 24.0h， 以1.26 g的产率得到9,10-di-tert-butyldimethylsilyloxystearic acid ethyl ester
  参考文献：
  名称：

  Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters

  摘要：

  Several efficient synthetic routes giving readily access to (oxy)-sitosterol esters and (oxy)cholesterol esters derived respectively from oleic acid and from 9,10-dihydroxystearic acid were developed for the first time. This approach allowed that sufficient amounts of the latter were available in order to carry out further biological studies. (c) 2008 Elsevier Inc. All rights reserved.

  DOI：

  10.1016/j.steroids.2008.04.010