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trans-2-Brom-N,N-bis-(trifluormethyl)-vinylamin | 19483-20-6

中文名称
——
中文别名
——
英文名称
trans-2-Brom-N,N-bis-(trifluormethyl)-vinylamin
英文别名
trans-2-Brom-N,N-bis-trifluormethyl-vinylamin;trans-2-bromo-N,N-bis(trifluoromethyl) vinylamine;(E)-2-bromo-N,N-bis(trifluoromethyl)ethenamine
trans-2-Brom-N,N-bis-(trifluormethyl)-vinylamin化学式
CAS
19483-20-6
化学式
C4H2BrF6N
mdl
——
分子量
257.961
InChiKey
MNCAYYXFVJUQBE-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:
    56.0±40.0 °C(Predicted)
  • 密度:
    1.824±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    参考文献:
    名称:
    氟化乙炔。I部分的制备NN -bistrifluoromethylethynylamines
    摘要:
    NN -Bistrifluoromethylethynylamine,(CF 3)2 N·Ç⋮CH,已在通过反应高产率制备Ñ -bromobistrifluoromethylamine与乙炔,然后将所得1的脱溴化氢:1加合物,2-溴- NN -bistrifluoromethylvinylamine 。的bistrifluoromethylvinylamine溴化以得到1,2-二溴- NN -bistrifluoromethylethylamine和这种加合物的脱溴化氢,由烯烃1-溴方式NN -双trifluoromethylvinylamine,也给出了乙炔。Ñ与-Bromobistrifluoromethylamine发生反应NN -bistrifluoromethylethynylamine,得到1,2-二(bistrifluoromethylamino)-1-溴乙烯,(CF3) 2
    DOI:
    10.1039/j39680001096
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文献信息

  • Fluorinated acetylenes. Part II. Certain ionic and radical additions to NN-bistrifluoromethylethynylamine
    作者:J. Freear、A. E. Tipping
    DOI:10.1039/j39690000411
    日期:——
    NN-bistrifluoromethylethynylamine with alkaline hypobromite. Bromo-NN-bistrifluoromethylethynylamine reacts with hydrogen bromide in the dark to give only cis-1,2-dibromo-NN-bistrifluoromethylvinyl-amine. The acid-catalysed hydration of NN-bistrifluoromethylethynylamine gives NN-bistrifluoromethylacetamide and hydrogenation yields NN-bistrifluoromethylvinylamine. NN-Bistrifluoromethylethynylamine does not react with
    NN与溴化氢或在黑暗溴-Bistrifluoromethylethynylamine反应,得到1-溴NN -Bistrifluoromethylvinylamine或反式-1,2-二溴NN -bistrifluoromethylvinylamine,分别。在光解条件下,产物分别是顺式和反式-2-溴-NN-双三氟甲基乙烯基胺(比率34:66)和顺式和反式-1,2-二溴-NN-双三氟甲基乙烯基胺(比率64:36)。单独在光解作用下的反式-1,2-二溴-NN-双三氟甲基乙烯基胺会部分异构化,得到顺式-和反式的比例64烯烃:36. 1,2-二溴-的混合物的脱溴化氢NN -bistrifluoromethylvinylamine异构体给出溴NN -bistrifluoromethylethynylamine以良好的收率和本乙炔也由反应形成的NN -双三氟甲基乙炔胺与碱性次溴酸盐。溴-NN-双三氟甲基
  • Fluorinated acetylenes. Part I. The preparation of NN-bistrifluoromethylethynylamines
    作者:J. Freear、A. E. Tipping
    DOI:10.1039/j39680001096
    日期:——
    NN-Bistrifluoromethylethynylamine, (CF3)2N·C⋮CH, has been prepared in high yield by the reaction of N-bromobistrifluoromethylamine with acetylene, followed by dehydrobromination of the resultant 1 : 1-adduct, 2-bromo-NN-bistrifluoromethylvinylamine. The bromination of bistrifluoromethylvinylamine to give 1,2-dibromo-NN-bistrifluoromethylethylamine and the dehydrobromination of this adduct, by way of
    NN -Bistrifluoromethylethynylamine,(CF 3)2 N·Ç⋮CH,已在通过反应高产率制备Ñ -bromobistrifluoromethylamine与乙炔,然后将所得1的脱溴化氢:1加合物,2-溴- NN -bistrifluoromethylvinylamine 。的bistrifluoromethylvinylamine溴化以得到1,2-二溴- NN -bistrifluoromethylethylamine和这种加合物的脱溴化氢,由烯烃1-溴方式NN -双trifluoromethylvinylamine,也给出了乙炔。Ñ与-Bromobistrifluoromethylamine发生反应NN -bistrifluoromethylethynylamine,得到1,2-二(bistrifluoromethylamino)-1-溴乙烯,(CF3) 2
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