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(S)-2-(perfluoropropyl)octan-1-ol | 1180131-15-0

中文名称
——
中文别名
——
英文名称
(S)-2-(perfluoropropyl)octan-1-ol
英文别名
——
(S)-2-(perfluoropropyl)octan-1-ol化学式
CAS
1180131-15-0
化学式
C11H17F7O
mdl
——
分子量
298.244
InChiKey
WMACVQXHKHMJTO-QMMMGPOBSA-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):
    4.4
  • 重原子数:
    19.0
  • 可旋转键数:
    8.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.23
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Enantioselective α-Trifluoromethylation of Aldehydes via Photoredox Organocatalysis
    摘要:
    The first enantioselective, organocatalytic alpha-trifluoromethytation and alpha-perfluoroalkylation of aldehydes have been accomplished using a readily available iridium photocatalyst and a chiral imidazolidinone catalyst. A range of alpha-trifluoromethyl and alpha-perfluoroalkyl aldehydes were obtained from commercially available perfluoroalkyl halides with high efficiency and enantioselectivity. The resulting alpha-trifluoromethyl aldehydes were subsequently shown to be versatile precursors for the construction of a variety of enantioenriched trifluoromethylated building blocks.
    DOI:
    10.1021/ja9053338
  • 作为产物:
    描述:
    在 sodium tetrahydroborate 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 1.0h, 以0.155 g的产率得到(S)-2-(perfluoropropyl)octan-1-ol
    参考文献:
    名称:
    Enantioselective α-Trifluoromethylation of Aldehydes via Photoredox Organocatalysis
    摘要:
    The first enantioselective, organocatalytic alpha-trifluoromethytation and alpha-perfluoroalkylation of aldehydes have been accomplished using a readily available iridium photocatalyst and a chiral imidazolidinone catalyst. A range of alpha-trifluoromethyl and alpha-perfluoroalkyl aldehydes were obtained from commercially available perfluoroalkyl halides with high efficiency and enantioselectivity. The resulting alpha-trifluoromethyl aldehydes were subsequently shown to be versatile precursors for the construction of a variety of enantioenriched trifluoromethylated building blocks.
    DOI:
    10.1021/ja9053338
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