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trans-1-fluoro-2-iodoethylene | 2353-82-4

中文名称
——
中文别名
——
英文名称
trans-1-fluoro-2-iodoethylene
英文别名
trans-1-fluoro-2-iodo-ethene;trans-2-Fluor-1-jod-aethylen;(E)-1-fluoro-2-iodoethene
trans-1-fluoro-2-iodoethylene化学式
CAS
2353-82-4
化学式
C2H2FI
mdl
——
分子量
171.941
InChiKey
UBWJYLSNGVHRSE-OWOJBTEDSA-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:
    64-65 °C
  • 密度:
    2.164±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    4
  • 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:
    1

反应信息

  • 作为产物:
    描述:
    (E/z)-1-溴-2-氟乙烯 、 sodium iodide 作用下, 反应 44.0h, 生成 1,1-二氟乙烷氟化乙烯 、 cis-1-fluoro-2-iodoethylene 、 trans-1-fluoro-2-iodoethylene
    参考文献:
    名称:
    Efficient Microscale Preparation of Isotopically Enriched 1‐[79Br]Bromo‐2‐Fluoroethylene, [79Br]BrHC˭CHF
    摘要:
    An efficient preparation of 1-[Br-79]bromo-2-fluoroethylene, [Br-79]BrHC=CHF, was carried out by a three-step procedure: (a) natural 1-bromo-2-fluoroethylene, BrHC=CHF, was iodinated to 1-fluoro-2-iodoethylene, FHC=CHI; (b) 1-fluoro-2-iodoethylene was Br-79(2)-brominated to 1,2-di[Br-79]bromo-1-fluoro-2-iodoethane, [Br-79]BrFCHCH[Br-79]BrI; ad (c) 1,2-di[Br-79]bromo-1-fluoro-2-iodoethane was dehalogenated to 1-[Br-79]bromo-2-fluoroethylene, [Br-79] BrHC=CHF. The yield of isolated product, on a 2-mmol scale, was 62% with respect to B-79(2).
    DOI:
    10.1081/scc-200057980
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文献信息

  • Efficient Microscale Preparation of Isotopically Enriched 1‐[<sup>79</sup>Br]Bromo‐2‐Fluoroethylene, [<sup>79</sup>Br]BrHC˭CHF
    作者:Alessandro Baldan、Augusto Tassan
    DOI:10.1081/scc-200057980
    日期:2005.6
    An efficient preparation of 1-[Br-79]bromo-2-fluoroethylene, [Br-79]BrHC=CHF, was carried out by a three-step procedure: (a) natural 1-bromo-2-fluoroethylene, BrHC=CHF, was iodinated to 1-fluoro-2-iodoethylene, FHC=CHI; (b) 1-fluoro-2-iodoethylene was Br-79(2)-brominated to 1,2-di[Br-79]bromo-1-fluoro-2-iodoethane, [Br-79]BrFCHCH[Br-79]BrI; ad (c) 1,2-di[Br-79]bromo-1-fluoro-2-iodoethane was dehalogenated to 1-[Br-79]bromo-2-fluoroethylene, [Br-79] BrHC=CHF. The yield of isolated product, on a 2-mmol scale, was 62% with respect to B-79(2).
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