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2-allylperfluorocyclobutanone | 155581-08-1

中文名称
——
中文别名
——
英文名称
2-allylperfluorocyclobutanone
英文别名
(2-allyl-)pentafluorocyclobutanone;2,2,3,3,4-Pentafluoro-4-(prop-2-en-1-yl)cyclobutan-1-one;2,2,3,3,4-pentafluoro-4-prop-2-enylcyclobutan-1-one
2-allylperfluorocyclobutanone化学式
CAS
155581-08-1
化学式
C7H5F5O
mdl
——
分子量
200.108
InChiKey
GPRHZWGNLMVWCH-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

物化性质

  • 沸点:
    115.9±40.0 °C(Predicted)
  • 密度:
    1.37±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    2-allylperfluorocyclobutanone 、 alkaline earth salt of/the/ methylsulfuric acid 以 various solvent(s) 为溶剂, 反应 0.25h, 以22%的产率得到2-(allyl)-1-methyleneperfluorocyclobutene
    参考文献:
    名称:
    Energetics of Fluoroalkene Double Bond Isomerizations
    摘要:
    The effects of perfluorination of cyclic and acyclic alkenes have been examined. Quantum mechanical calculations and experimental data show that vicinally substituted acyclic alkenes are strongly destabilized by fluorination. Quite surprisingly, the destabilization is much smaller for cyclic analogs. This difference has dramatic consequences for the relative stabilities of double bond isomers in cyclic and acyclic systems, including keto-enol systems. The reasons for the contrast are discussed in detail.
    DOI:
    10.1021/ja963789f
  • 作为产物:
    描述:
    六氟环丁烯氢氧化钾 作用下, 以 为溶剂, 生成 2-allylperfluorocyclobutanone
    参考文献:
    名称:
    Copolymerizable fluorinated compounds, a process for their preparation
    摘要:
    公式为##STR1##的2-烯丙基-全氟烷基-三氟乙烯醚,其中R.sup.1.sub.F和R.sup.2.sub.F表示--CF.sub.3或者一起表示(CF.sub.2).sub.n,其中n=2或3。
    公开号:
    US05313003A1
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文献信息

  • US5313003A
    申请人:——
    公开号:US5313003A
    公开(公告)日:1994-05-17
  • US5399645A
    申请人:——
    公开号:US5399645A
    公开(公告)日:1995-03-21
  • Copolymerizable fluorinated compounds, a process for their preparation
    申请人:Bayer Aktiengesellschaft
    公开号:US05313003A1
    公开(公告)日:1994-05-17
    A 2-allyl-perfluoroalkyl-trifluorovinyl ether of the formula ##STR1## wherein R.sup.1.sub.F and R.sup.2.sub.F represent either --CF.sub.3 or, together, (CF.sub.2).sub.n where n=2 or 3.
    公式为##STR1##的2-烯丙基-全氟烷基-三氟乙烯醚,其中R.sup.1.sub.F和R.sup.2.sub.F表示--CF.sub.3或者一起表示(CF.sub.2).sub.n,其中n=2或3。
  • Energetics of Fluoroalkene Double Bond Isomerizations
    作者:Patrick E. Lindner、David M. Lemal
    DOI:10.1021/ja963789f
    日期:1997.4.1
    The effects of perfluorination of cyclic and acyclic alkenes have been examined. Quantum mechanical calculations and experimental data show that vicinally substituted acyclic alkenes are strongly destabilized by fluorination. Quite surprisingly, the destabilization is much smaller for cyclic analogs. This difference has dramatic consequences for the relative stabilities of double bond isomers in cyclic and acyclic systems, including keto-enol systems. The reasons for the contrast are discussed in detail.
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