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1,1,1,2,2,3,5,6,7,7,7-undecafluoro-3,5-bis(fluorosulfonyloxy)-4-oxo-6-(trifluoromethyl)heptane | 143582-74-5

中文名称
——
中文别名
——
英文名称
1,1,1,2,2,3,5,6,7,7,7-undecafluoro-3,5-bis(fluorosulfonyloxy)-4-oxo-6-(trifluoromethyl)heptane
英文别名
——
1,1,1,2,2,3,5,6,7,7,7-undecafluoro-3,5-bis(fluorosulfonyloxy)-4-oxo-6-(trifluoromethyl)heptane化学式
CAS
143582-74-5
化学式
C8F16O7S2
mdl
——
分子量
576.19
InChiKey
SUPFKOPGXSJFPJ-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):
    3.38
  • 重原子数:
    33.0
  • 可旋转键数:
    8.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    103.81
  • 氢给体数:
    0.0
  • 氢受体数:
    7.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    perfluoro-6-methylhept-4-en-3-one 在 sodium fluorosulfonate氟磺酸 、 cesium fluoride 作用下, 以 二乙二醇二甲醚 为溶剂, 反应 15.0h, 生成 1,1,1,2,2,3,5,6,7,7,7-undecafluoro-3,5-bis(fluorosulfonyloxy)-4-oxo-6-(trifluoromethyl)heptane
    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.
  • Perfluorinated α,β-unsaturated thyocyanats: synthesis, molecular rearrangements, intramolecular heterocyclizations
    作者:Vera Ya. Popkova
    DOI:10.1016/s0022-1139(00)83816-6
    日期:1991.9
  • 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.
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