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triethenylstannane | 163273-06-1

中文名称
——
中文别名
——
英文名称
triethenylstannane
英文别名
tris(ethenyl)stannane
triethenylstannane化学式
CAS
163273-06-1
化学式
C6H10Sn
mdl
——
分子量
200.855
InChiKey
ZBTNNYHWNLQCPH-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):
    1.39
  • 重原子数:
    7.0
  • 可旋转键数:
    3.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0.0
  • 氢给体数:
    0.0
  • 氢受体数:
    0.0

反应信息

  • 作为产物:
    描述:
    dichloroaluminum hydride氯三乙烯基锡烷 以 not given 为溶剂, 生成 triethenylstannane
    参考文献:
    名称:
    Vinylstannanes: synthesis and characterization
    摘要:
    Primary, secondary and tertiary vinylstannanes 2a-2f are synthesized by reduction of the corresponding chloro(vinyl)stannanes. They are characterized by their spectral data (IR, NMR (Sn-119, C-13, H-1) spectroscopy and mass spectrometry). The Sn-119 chemical shifts and (1)J(SnH) and (1)J(SnC) of vinylstannanes are compared with the data reported for the corresponding alkyl- and aryl-stannanes. Compounds 2 decompose slowly at room temperature in benzene (tau(1/2) 1-3 days). The formation of divinylchlorostannane and the use of trivinylstannane as a reducing agent are also reported.
    DOI:
    10.1016/0022-328x(94)05057-i
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文献信息

  • Vinylstannanes: synthesis and characterization
    作者:Tajdine Janati、Jean-Claude Guillemin、Mohammed Soufiaoui
    DOI:10.1016/0022-328x(94)05057-i
    日期:1995.1
    Primary, secondary and tertiary vinylstannanes 2a-2f are synthesized by reduction of the corresponding chloro(vinyl)stannanes. They are characterized by their spectral data (IR, NMR (Sn-119, C-13, H-1) spectroscopy and mass spectrometry). The Sn-119 chemical shifts and (1)J(SnH) and (1)J(SnC) of vinylstannanes are compared with the data reported for the corresponding alkyl- and aryl-stannanes. Compounds 2 decompose slowly at room temperature in benzene (tau(1/2) 1-3 days). The formation of divinylchlorostannane and the use of trivinylstannane as a reducing agent are also reported.
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