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threo-5,6-dimethyldecane | 1636-43-7

中文名称
——
中文别名
——
英文名称
threo-5,6-dimethyldecane
英文别名
racemic 5,6-dimethyldecane;(5R,6R)-5,6-dimethyldecane
threo-5,6-dimethyldecane化学式
CAS
1636-43-7;42850-30-6;42920-83-2;54829-10-6
化学式
C12H26
mdl
——
分子量
170.338
InChiKey
NCJIZIYQFWXMFZ-VXGBXAGGSA-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:
    -50.8°C (estimate)
  • 沸点:
    201°C
  • 密度:
    0.7567

计算性质

  • 辛醇/水分配系数(LogP):
    6.1
  • 重原子数:
    12
  • 可旋转键数:
    7
  • 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

安全信息

  • 海关编码:
    2901100000

SDS

SDS:8f5abd07a1d696091e0112284ff0e977
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反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and conversions of metallocycles. 7. A novel approach to the synthesis of 3,4-dialkyl-substituted aluminacyclopentanes in the presence of Cp2ZrCl2
    摘要:
    A novel approach was developed for the stereoselective synthesis of trans-3,4-dialkyl-substituted aluminacyclopentanes from alpha-olefins, metallic magnesium, and EtAlCl2 in the presence of catalytic amounts of CP2ZrCl2. The hydrolysis and deuterolysis products of the 3,4-dialkyl-substituted aluminacyclopentanes obtained are only in the trans configuration.
    DOI:
    10.1007/bf00961245
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文献信息

  • Synthesis and conversions of metallocycles. 7. A novel approach to the synthesis of 3,4-dialkyl-substituted aluminacyclopentanes in the presence of Cp2ZrCl2
    作者:U. M. Dzhemilev、A. G. Ibragimov、A. B. Morozov、R. R. Muslukhov、G. A. Tolstikov
    DOI:10.1007/bf00961245
    日期:1991.7
    A novel approach was developed for the stereoselective synthesis of trans-3,4-dialkyl-substituted aluminacyclopentanes from alpha-olefins, metallic magnesium, and EtAlCl2 in the presence of catalytic amounts of CP2ZrCl2. The hydrolysis and deuterolysis products of the 3,4-dialkyl-substituted aluminacyclopentanes obtained are only in the trans configuration.
  • Synthesis and transformations of metallocycles. 9. Regioselective and stereoselective synthesis of al-substitutedtrans-3,4-dialkylaluminocyclopentanes catalyzed by (?5-C5H5)2ZrCl2
    作者:U. M. Dzhemilev、A. G. Ibragimov、A. B. Morozov、R. R. Muslukhov、G. A. Tolstikov
    DOI:10.1007/bf00866593
    日期:1992.6
    A new stereoselective method is developed for the synthesis of 1-chloro-, 1-alkoxy-, and 1-N,N-dialkylaminoalumino-cyclopentanes from alpha-olefins, metallic magnesium, and aluminum halides (AlCl3, RO-AlCl2, R2N-AlCl2) in the presence of catalytic amounts of Cp2ZrCl2 (Cp = eta5-C5H5). The products from hydrolysis and deuterolysis of the Al-substituted 3,4-dialkylaluminocyclopentanes (ACP) have the threo configuration.
  • Synthesis and reactions of metallocycles. 6. Stereoselective synthesis of 3,4-dialkyl-substituted aluminocyclopentanes by cyclometallation of ?-olefins using trialkylalanes in the presence of Cp2ZrCl2
    作者:U. M. Dzhemilev、A. G. Ibragimov、A. B. Morozov、L. M. Khalilov、R. R. Muslukhov、G. A. Tolstikov
    DOI:10.1007/bf00961366
    日期:1991.5
    An efficient method has been developed for the synthesis of a new class of organo-aluminum compounds, trans-3,4-dialkyl-substituted aluminocyclopentanes, via the cyclometallation of alpha-olefins using R3Al in the presence of catalytic amounts of Cp2ZrCl2. Hydrolysis, deuterolysis, and oxidation of the resulting aluminocyclopentanes generate the corresponding transformation products having exclusively the threo-configuration.
  • DZHEMILEV, U. M.;IBRAGIMOV, A. G.;MOROZOV, A. B.;XALILOV, L. M.;MUSLUXOV,+, IZV. AN CCCP. CEP. XIM.,(1991) N, S. 1141-1144
    作者:DZHEMILEV, U. M.、IBRAGIMOV, A. G.、MOROZOV, A. B.、XALILOV, L. M.、MUSLUXOV,+
    DOI:——
    日期:——
  • Regio- and stereoselective synthesis for a novel class of organoaluminium compounds — substituted aluminacyclopentanes and aluminacyclopentenes assis
    作者:U.M. Dzhemilev、A.G. Ibragimov
    DOI:10.1016/0022-328x(94)88022-0
    日期:1994.2
    A novel regio- and stereoselective method has been developed for the catalytic cyclometallation of olefins and acetylenes with alkylalanes in the presence of Cp(2)ZrCl(2), to give in one stage high yields of 3-substituted aluminacyclopentanes and aluminacyclopentenes. Applications of these reactions to a wide range of linear and cyclic olefins and to those containing functional substituents have been studied. The transformation of the aluminacyclopentanes thus produced, into five-membered heterocycles, mono- and di-substituted cyclobutanes and cyclopropanes, has been demonstrated.
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