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1-bromo-3-chloro-1,1,3,3-tetrafluoropropane | 460-87-7

中文名称
——
中文别名
——
英文名称
1-bromo-3-chloro-1,1,3,3-tetrafluoropropane
英文别名
1-bromo-3-chloro-1,1,3,3-tetrafluoro-propane;1-Brom-3-chlor-1,1,3,3-tetrafluor-propan
1-bromo-3-chloro-1,1,3,3-tetrafluoropropane化学式
CAS
460-87-7
化学式
C3H2BrClF4
mdl
——
分子量
229.399
InChiKey
IYZDWHRLNGZSAI-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:
    79 °C
  • 密度:
    1.7890 g/cm3(Temp: 25 °C)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1-bromo-3-chloro-1,1,3,3-tetrafluoropropane氢氧化钾四丁基氢氧化铵 作用下, 以83%的产率得到3-氯-1,1,3,3-四氟-1-丙烯
    参考文献:
    名称:
    Perfluoro-4-methyl-1,3-dioxole: a new monomer for high-Tg amorphous fluoropolymers
    摘要:
    A 4-Chloro-5-trifluoromethyl-2,2,4-trifluoro-1,3-dioxolane (1) was synthesised by reaction of CF2(OF)(2) with CF3-CH=CFCl; the elimination of HCl from (1) in basic conditions led to the formation of dioxole perfluoro-4-methyl-1,3-dioxole (2). Both these synthetic steps gave the corresponding product in high yield.A new synthetic route for the preparation of CF3-CH=CFCl, starting from CF2ClBr and CH2=CF2, together with some examples of polymerisation products obtained by reaction of dioxole (2) with fluoroolefins are also reported. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2003.10.009
  • 作为产物:
    描述:
    二氟一氯溴甲烷偏氟乙烯二叔丁基过氧化物 作用下, 110.0 ℃ 、2.03 MPa 条件下, 反应 8.0h, 以62%的产率得到1-bromo-3-chloro-1,1,3,3-tetrafluoropropane
    参考文献:
    名称:
    Perfluoro-4-methyl-1,3-dioxole: a new monomer for high-Tg amorphous fluoropolymers
    摘要:
    A 4-Chloro-5-trifluoromethyl-2,2,4-trifluoro-1,3-dioxolane (1) was synthesised by reaction of CF2(OF)(2) with CF3-CH=CFCl; the elimination of HCl from (1) in basic conditions led to the formation of dioxole perfluoro-4-methyl-1,3-dioxole (2). Both these synthetic steps gave the corresponding product in high yield.A new synthetic route for the preparation of CF3-CH=CFCl, starting from CF2ClBr and CH2=CF2, together with some examples of polymerisation products obtained by reaction of dioxole (2) with fluoroolefins are also reported. (C) 2003 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2003.10.009
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文献信息

  • Free Radical Additions Involving Fluorine Compounds. III. The Addition of Bromochlorodifluoromethane to Olefins<sup>1,2</sup>
    作者:Paul Tarrant、Alan M. Lovelace
    DOI:10.1021/ja01608a076
    日期:1955.2.1
  • Perfluoro-4-methyl-1,3-dioxole: a new monomer for high-Tg amorphous fluoropolymers
    作者:Antonio Russo、Walter Navarrini
    DOI:10.1016/j.jfluchem.2003.10.009
    日期:2004.1
    A 4-Chloro-5-trifluoromethyl-2,2,4-trifluoro-1,3-dioxolane (1) was synthesised by reaction of CF2(OF)(2) with CF3-CH=CFCl; the elimination of HCl from (1) in basic conditions led to the formation of dioxole perfluoro-4-methyl-1,3-dioxole (2). Both these synthetic steps gave the corresponding product in high yield.A new synthetic route for the preparation of CF3-CH=CFCl, starting from CF2ClBr and CH2=CF2, together with some examples of polymerisation products obtained by reaction of dioxole (2) with fluoroolefins are also reported. (C) 2003 Elsevier B.V. All rights reserved.
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