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1-(2,2,3,3-tetrafluoropropyloxy)-2-methylpropane | 1115941-61-1

中文名称
——
中文别名
——
英文名称
1-(2,2,3,3-tetrafluoropropyloxy)-2-methylpropane
英文别名
1-(2,2,3,3-Tetrafluoropropyloxy)-2-methylpropane;2-methyl-1-(2,2,3,3-tetrafluoropropoxy)propane
1-(2,2,3,3-tetrafluoropropyloxy)-2-methylpropane化学式
CAS
1115941-61-1
化学式
C7H12F4O
mdl
——
分子量
188.165
InChiKey
QRMZVGDEYISIRA-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):
    2.9
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    异丁醇2,2,3,3-Tetrafluoropropyl chlorosulfiteN,N-二甲基甲酰胺 作用下, 以60%的产率得到1-(2,2,3,3-tetrafluoropropyloxy)-2-methylpropane
    参考文献:
    名称:
    Features of catalysis in the reaction of polyfluoroalkyl chlorosulfites with saturated monohydric alcohols
    摘要:
    Synthetic opportunities and mechanism of catalysis of the reaction of polyfluororalkylchlorosulfites with saturated monohydric alcohols are considered. Kinetic measurements and quantum-chemical calculations showed that polyfluoroalkylation of these compounds proceeded through the step of complex formation involving reagents and catalyst followed by liberation of hydrogen chloride and sulfur dioxide and formation of polyfluoroalkyl ethers.
    DOI:
    10.1134/s1070363208110169
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文献信息

  • Features of catalysis in the reaction of polyfluoroalkyl chlorosulfites with saturated monohydric alcohols
    作者:A. I. Rakhimov、A. V. Nalesnaya、R. V. Fisechko
    DOI:10.1134/s1070363208110169
    日期:2008.11
    Synthetic opportunities and mechanism of catalysis of the reaction of polyfluororalkylchlorosulfites with saturated monohydric alcohols are considered. Kinetic measurements and quantum-chemical calculations showed that polyfluoroalkylation of these compounds proceeded through the step of complex formation involving reagents and catalyst followed by liberation of hydrogen chloride and sulfur dioxide and formation of polyfluoroalkyl ethers.
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