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1,2-bis-fluorosulfatoperfluoro-3-methylpentanois acid fluoride | 143582-63-2

中文名称
——
中文别名
——
英文名称
1,2-bis-fluorosulfatoperfluoro-3-methylpentanois acid fluoride
英文别名
α,β-bisfluorosulfatoperfluoroisocaproyl fluoride;2,3-bis-fluorosulfatoperfluoro-4-methylpentanoyl fluoride;2,3,4,5,5,5-hexafluoro-2,3-bis(fluorosulfonyloxy)-4-(trifluoromethyl)pentanoyl fluoride
1,2-bis-fluorosulfatoperfluoro-3-methylpentanois acid fluoride化学式
CAS
143582-63-2
化学式
C6F12O7S2
mdl
——
分子量
476.175
InChiKey
RAWPNGLHXLEIGD-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):
    2.11
  • 重原子数:
    27.0
  • 可旋转键数:
    7.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    103.81
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,2-bis-fluorosulfatoperfluoro-3-methylpentanois acid fluoride氢氧化钾 作用下, 以 乙腈 为溶剂, 以75%的产率得到1-fluorosulfatoperfluoro-3-methyl-1-butene
    参考文献:
    名称:
    Synthesis of fluorovinyl fluorosulfonates
    摘要:
    DOI:
    10.1007/bf00866607
  • 作为产物:
    描述:
    4-trifluoromethylperfluoro-2-pentenoic acid fluoridesodium fluorosulfonate氟磺酸 作用下, 以 为溶剂, 反应 14.0h, 以83%的产率得到1,2-bis-fluorosulfatoperfluoro-3-methylpentanois acid fluoride
    参考文献:
    名称:
    Interaction of perfluorinated α-fluorosulfatocarbonyl compounds with nucleophilic reagents
    摘要:
    alpha-Perfluorosulfatoperfluorocarbonyl compounds interact with alkaline metals halogenides to form the corresponding alpha-halo derivatives as a result of the direct nucleophilic substitution of the FSO3 group. Through the action of halogenide anions on perfluorinated alpha,beta-bis-fluorosulfatocarbonyl compounds, substitution by halogen of the FSO3 group in the alpha-position to the carbonyl takes place. However, the FSO3 group in the beta-position is cleaved, which allows alpha-substituted beta-dicarbonyl derivatives to be obtained.
    DOI:
    10.1016/s0022-1139(00)80858-1
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文献信息

  • Fluoroaliphatic esters of fluorosulfonic acid. 6. Interaction of fluorine-containing ?,?-bis-fluorosulfatocarbonyl compounds with nucleophilic reagents
    作者:V. M. Rogovik、N. I. Delyagina、A. F. A�rov、V. F. Cherstkov、S. R. Sterlin、L. S. German
    DOI:10.1007/bf00863085
    日期:1992.3
    Fluorine-containing alpha,beta-fluorosulfatocarbonyl compounds interact with halides of alkali metals with the formation of alpha-halogeno-beta-dicarbonyl derivatives.
  • Interaction of perfluorinated α-fluorosulfatocarbonyl compounds with nucleophilic reagents
    作者:N.I. Delyagina、E.A. Avetisyan、V.M. Rogovik、V.F. Cherstkov、S.R. Sterlin、L.S. German
    DOI:10.1016/s0022-1139(00)80858-1
    日期:1993.12
    alpha-Perfluorosulfatoperfluorocarbonyl compounds interact with alkaline metals halogenides to form the corresponding alpha-halo derivatives as a result of the direct nucleophilic substitution of the FSO3 group. Through the action of halogenide anions on perfluorinated alpha,beta-bis-fluorosulfatocarbonyl compounds, substitution by halogen of the FSO3 group in the alpha-position to the carbonyl takes place. However, the FSO3 group in the beta-position is cleaved, which allows alpha-substituted beta-dicarbonyl derivatives to be obtained.
  • Synthesis of fluorovinyl fluorosulfonates
    作者:N. I. Delyagina、V. F. Cherstkov、S. R. Sterlin、L. S. German
    DOI:10.1007/bf00866607
    日期:1992.6
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