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1,1,2,3,3-五氟丙-1-烯 | 38683-48-6

中文名称
1,1,2,3,3-五氟丙-1-烯
中文别名
——
英文名称
1,1,2,3,3-pentafluoro-prop-1->3-enyl
英文别名
pentafluoroallyl;Allyl, pentafluoro-, radical
1,1,2,3,3-五氟丙-1-烯化学式
CAS
38683-48-6
化学式
C3F5
mdl
——
分子量
131.025
InChiKey
VRLCFIBHVFTRES-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):
    1.6
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:beacab464b91f36f9548cec83f998aaf
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反应信息

  • 作为产物:
    描述:
    Perfluoro-1,5-hexadiene 850.0 ℃ 、1.33 Pa 条件下, 生成 全氟丙二烯1,1,2,3,3-五氟丙-1-烯
    参考文献:
    名称:
    Electron impact fragmentation and primary vacuum pyrolysis products of isomeric perfluorocarbons of composition C6F10 and their hydrocarbon analogs C6H10
    摘要:
    DOI:
    10.1007/bf00961099
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文献信息

  • Infrared multiphoton dissociation of two perfluorobutenes
    作者:Cheryl A. Longfellow、Cindy L. Berrie、Arthur G. Suits、Yuan T. Lee
    DOI:10.1063/1.474960
    日期:1997.11.8
    Photofragment translational spectroscopy was used to examine the infrared multiphoton dissociation of octafluoro-1-butene and octafluoro-2-butene. The predominant unimolecular reaction in octafluoro-1-butene at moderate laser fluences is cleavage of a carbon–carbon single bond to give the products CF3 and C3F5. The two other reactions that take place are CF2 elimination and the formation of equal weight fragments with the chemical composition C2F4; both reactions take place via a diradical intermediate. Dissociation of octafluoro-1-butene to the resonance stabilized perfluoroallyl radical is suggested to account for the favoring of simple bond rupture. These three reaction pathways were also observed in octafluoro-2-butene dissociation, however, the branching fraction is different than from octafluoro-1-butene. In octafluoro-2-butene all three channels occur with roughly equal probability. The reactions involving CF2 loss and C2F4 formation in octafluoro-2-butene are thought to proceed through the same diradical intermediate as in octafluoro-1-butene, necessitating a 1,2-fluorine migration.
  • Electron impact fragmentation and primary vacuum pyrolysis products of isomeric perfluorocarbons of composition C6F10 and their hydrocarbon analogs C6H10
    作者:N. D. Kagramanov、I. O. Bragilevskii、A. K. Mal'tsev
    DOI:10.1007/bf00961099
    日期:1988.8
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