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9,10-di-tert-butyldimethylsilyloxystearic acid | 1131964-21-0

中文名称
——
中文别名
——
英文名称
9,10-di-tert-butyldimethylsilyloxystearic acid
英文别名
9,10-Bis[[tert-butyl(dimethyl)silyl]oxy]octadecanoic acid
9,10-di-tert-butyldimethylsilyloxystearic acid化学式
CAS
1131964-21-0
化学式
C30H64O4Si2
mdl
——
分子量
545.007
InChiKey
LWAZCSKDPHRJSL-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    10.33
  • 重原子数:
    36
  • 可旋转键数:
    22
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.97
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    9,10-di-tert-butyldimethylsilyloxystearic acid(24R)-5β,6β-epoxy-24-ethylcholestane-3β-ol4-二甲氨基吡啶N,N'-二环己基碳二亚胺 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以79%的产率得到(3S,4aS,5aR,6aS,6bS,9R,9aR,11aS,11bR)-9-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-9a,11b-dimethylhexadecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-3-yl 9,10-bis((tert-butyldimethylsilyl)oxy)octadecanoate
    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-di-tert-butyldimethylsilyloxystearic acid ethyl esterbarium 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
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