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difluoromethylcyclopentadecane | 1126749-02-7

中文名称
——
中文别名
——
英文名称
difluoromethylcyclopentadecane
英文别名
Difluoromethylcyclopentadecane
difluoromethylcyclopentadecane化学式
CAS
1126749-02-7
化学式
C16H30F2
mdl
——
分子量
260.411
InChiKey
UNCRKCXGQHEPPV-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):
    8.3
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2-cyclopentadecyl-1,3-dithiane三氟化溴 作用下, 以 一氟三氯甲烷 为溶剂, 以75%的产率得到difluoromethylcyclopentadecane
    参考文献:
    名称:
    Replacing the carbonyl's oxygen with the difluoromethyl group
    摘要:
    Aldehydes or ketones were reacted with 2-(trimethylsilyl)-1,3-dithiane (1) and the products reduced to the corresponding dithianes using tetrafluoroboric acid and sodium borohydride. These sulfur containing Compounds were reacted with bromine trifluoride under mild conditions (1-2 min, 0 C) with a net result of replacing the carbonyls' oxygen with the desired difluoromethyl moiety. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.12.042
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文献信息

  • Replacing the carbonyl's oxygen with the difluoromethyl group
    作者:Or Cohen、Youlia Hagooly、Shlomo Rozen
    DOI:10.1016/j.tet.2008.12.042
    日期:2009.2
    Aldehydes or ketones were reacted with 2-(trimethylsilyl)-1,3-dithiane (1) and the products reduced to the corresponding dithianes using tetrafluoroboric acid and sodium borohydride. These sulfur containing Compounds were reacted with bromine trifluoride under mild conditions (1-2 min, 0 C) with a net result of replacing the carbonyls' oxygen with the desired difluoromethyl moiety. (C) 2008 Elsevier Ltd. All rights reserved.
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