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Triisopropylgermylketene | 386705-37-9

中文名称
——
中文别名
——
英文名称
Triisopropylgermylketene
英文别名
——
Triisopropylgermylketene化学式
CAS
386705-37-9
化学式
C11H22GeO
mdl
——
分子量
242.885
InChiKey
BWLOKCOUGBYMKN-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):
    3.59
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    Triisopropylgermylketene三氟甲磺酸三甲基硅酯三乙胺 作用下, 以 乙醚 为溶剂, 以23%的产率得到trimethylsilyl(triisopropylgermyl)ketene
    参考文献:
    名称:
    摘要:
    Silylation of silyl- and germylketenes with trialkylsilyl triflates was studied. Either the corresponding bis-organoelement-substituted ketenes or mixtures of these compounds with isomeric (silyloxy)silylacetylenes were formed depending on the size of the substituents at the silicon or germanium atom (both in ketenes and triflates) and on the nature of the heteroelement. The resulting (silyloxy)silylacetylenes were isomerized into the corresponding bis-sitylketenes upon prolonged storage.
    DOI:
    10.1023/a:1011346024964
  • 作为产物:
    描述:
    (triisopropylgermyl)ethoxyacetylene正辛烷 为溶剂, 以53%的产率得到Triisopropylgermylketene
    参考文献:
    名称:
    摘要:
    Silylation of silyl- and germylketenes with trialkylsilyl triflates was studied. Either the corresponding bis-organoelement-substituted ketenes or mixtures of these compounds with isomeric (silyloxy)silylacetylenes were formed depending on the size of the substituents at the silicon or germanium atom (both in ketenes and triflates) and on the nature of the heteroelement. The resulting (silyloxy)silylacetylenes were isomerized into the corresponding bis-sitylketenes upon prolonged storage.
    DOI:
    10.1023/a:1011346024964
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文献信息

  • ——
    作者:S. V. Ponomarev、A. S. Zolotareva、R. N. Ezhov、Yu. V. Kuznetsov、V. S. Petrosyan
    DOI:10.1023/a:1011346024964
    日期:——
    Silylation of silyl- and germylketenes with trialkylsilyl triflates was studied. Either the corresponding bis-organoelement-substituted ketenes or mixtures of these compounds with isomeric (silyloxy)silylacetylenes were formed depending on the size of the substituents at the silicon or germanium atom (both in ketenes and triflates) and on the nature of the heteroelement. The resulting (silyloxy)silylacetylenes were isomerized into the corresponding bis-sitylketenes upon prolonged storage.
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