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氯甲基二甲基己基硅烷 | 73013-40-8

中文名称
氯甲基二甲基己基硅烷
中文别名
——
英文名称
chloromethyldimethylhexylsilane
英文别名
Dimethyl-chlormethyl-hexylsilan;Chloromethyl-hexyl-dimethylsilane;chloromethyl-hexyl-dimethylsilane
氯甲基二甲基己基硅烷化学式
CAS
73013-40-8
化学式
C9H21ClSi
mdl
——
分子量
192.804
InChiKey
CKSRYOVEFQHASJ-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:
    213.6±13.0 °C(predicted)
  • 密度:
    0.859±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.05
  • 重原子数:
    11
  • 可旋转键数:
    6
  • 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:
    0

反应信息

点击查看最新优质反应信息

文献信息

  • Regioselective Synthesis of 1,4-Di(organo)[60]fullerenes through DMF-assisted Monoaddition of Silylmethyl Grignard Reagents and Subsequent Alkylation Reaction
    作者:Yutaka Matsuo、Akihiko Iwashita、Yoko Abe、Chang-Zhi Li、Keiko Matsuo、Masahiko Hashiguchi、Eiichi Nakamura
    DOI:10.1021/ja8041299
    日期:2008.11.19
    Monoaddition of Grignard reagents, in particular tri(organo)silylmethyl magnesium chlorides, to [60]fullerene took place smoothly in the presence of dimethylformamideto produce (organo)(hydro)[60]fullerenes, (C60RH)-H-1, in good yield (up to 93% isolated yield). The hydrofullerene was then deprotonated to generate the corresponding anion, C60R-, which was then alkylated to obtain 58 pi-electron di(organo)[60]fullerenes, (C60RR2)-R-1, in good to high yield (up to 93% overall yield). The two-step methodology provides a wide variety of 1,4-di(organo)[60] fullerenes bearing the same or different organic addends on the [60] fullerene core. By changing the addends, one can control the chemical and physical properties of the compounds at the molecular and bulk levels.
  • Synthesis and investigation of the dipole moments of ?-(n-alkyldimethylsilyl)propionic acids
    作者:D. N. Andreev、G. S. Smirnova、L. L. Burshtein、T. P. Stepanova、V. P. Malinovskaya
    DOI:10.1007/bf00947552
    日期:1979.10
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