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四烯丙基锗烷 | 1793-91-5

中文名称
四烯丙基锗烷
中文别名
——
英文名称
tetraallylgermane
英文别名
(CH2CHCH2)4germane;tetraallylgermanium;Tetraallyl-german;tetrakis(prop-2-enyl)germane
四烯丙基锗烷化学式
CAS
1793-91-5
化学式
C12H20Ge
mdl
——
分子量
236.881
InChiKey
LGLLRRNQRDPDEE-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

  • 熔点:
    <0°C
  • 沸点:
    105°C 10mm
  • 密度:
    1,015 g/cm3
  • 闪点:
    70°C

计算性质

  • 辛醇/水分配系数(LogP):
    4.18
  • 重原子数:
    13
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • TSCA:
    No
  • 危险类别码:
    R36/37/38
  • 安全说明:
    S26,S36/37/39

SDS

SDS:5280a753c5b8a91e4a703c87bceeb050
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反应信息

  • 作为反应物:
    描述:
    四烯丙基锗烷正丁基锂二氯二茂锆 作用下, 以 四氢呋喃四氯化碳正己烷 为溶剂, 以42%的产率得到
    参考文献:
    名称:
    Preparation of Axially Chiral (Racemic) Spirosilanes and Spirogermanes by Selective Spirozirconation
    摘要:
    Chiral (racemic) functional spirosilanes or -germanes, containing two (or four) stereogenic centers, were synthesized by selective cyclozirconation (or spirozirconation) of di- and tetraallylsilanes and di- and tetraallylgermanes.
    DOI:
    10.1021/om990839r
  • 作为产物:
    描述:
    参考文献:
    名称:
    Mazerolles; Lesbre, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1959, vol. 248, p. 2018,2020
    摘要:
    DOI:
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文献信息

  • Scandium trifluoromethanesulfonate-catalyzed chemoselective allylation reactions of carbonyl compounds with tetraallylgermane in aqueous media
    作者:Takahiko Akiyama、Junko Iwai、Megumi Sugano
    DOI:10.1016/s0040-4020(99)00371-3
    日期:1999.6
    Scandium(III) triflate-catalyzed allylation of carbonyl compounds with tetraalylgermane proceeded readily in aqueous nitromethane to afford homoallyl alcohols in excellent to good yields. The presence of H2O is indispensable for the allylation of aldehydes to proceed smoothly. Aldehydes were allylated highly chemoselectively in the presence of ketone moieties.
    硝基甲烷溶液中,三氟甲磺酸((III)催化的羰基化合物与四烷基锗烷的烯丙基化反应容易进行,从而以极好的收率得到均烯丙基醇。H 2 O的存在对于醛的烯丙基化顺利进行必不可少。在酮部分存在下,醛被高度化学选择性烯丙基化。
  • Hot wire chemical vapor deposition of germanium selenide thin films for nonvolatile random access memory applications
    作者:D. Reso、M. Silinskas、M. Lisker、A. Schubert、E. P. Burte
    DOI:10.1063/1.3579192
    日期:2011.4.11
    Thin films of germanium selenide (GexSe100−x with 0
    硒化锗薄膜(GexSe100−x 与 0
  • Reactivity of dianionic hexacoordinate germanium complexes toward organometallic reagents. A new route to organogermanes
    作者:G. Cerveau、C. Chuit、R. J. P. Corriu、C. Reye
    DOI:10.1021/om00051a049
    日期:1991.5
    Lithium and potassium tris(benzene-1,2-diolato)germanates (2a and 2b, respectively) and potassium tris(butane-2,3-diolato)germanate (3) are easily prepared from GeO2 in quantitative yields. They are very reactive toward organometallic reagents, the reactivity depending on the ligands on the germanium. Complexes 2 react with an excess of Grignard reagent to give the corresponding tetraorganogermanes R4Ge while the less reactive complex 3 leads to the functional triorganogermanes R3GeX. Tetraorganogermanes can also be prepared from complex 2b by reaction with organic bromides in the presence of Mg (Barbier reaction). The influence of Cp2TiCl2 and MgBr2 on the reactivity of Grignard reagents with these complexes was also investigated: in both cases formation of triorganogermanes was favored.
  • Reactions of nucleophilic reagents with dianionic hexacoordinated germanium complexes: a new convenient route to functional organogermanes from germanium dioxide
    作者:G. Cerveau、C. Chuit、R. J. P. Corriu、C. Reye
    DOI:10.1021/om00093a038
    日期:1988.3
  • Reaction of vinylgermaniums with butadiene
    作者:S. R. Rafikov、I. M. Salimgareeva、N. G. Bogatova、O. Zh. Zhebarov、V. K. Mavrodiev、V. P. Yur'ev
    DOI:10.1007/bf00950026
    日期:1982.4
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