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1-(2-氯乙基)环己-1,4-二烯 | 343927-33-3

中文名称
1-(2-氯乙基)环己-1,4-二烯
中文别名
——
英文名称
1-(2-chloroethyl)-1,4-cyclohexadiene
英文别名
1-(2-chloroethyl)cyclohexa-1,4-diene;2'-chloroethyl-1,4-cyclohexadiene
1-(2-氯乙基)环己-1,4-二烯化学式
CAS
343927-33-3
化学式
C8H11Cl
mdl
——
分子量
142.628
InChiKey
PUQBCDWVBMEVOV-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:
    187.3±19.0 °C(Predicted)
  • 密度:
    1.018±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,2-二甲基咪唑1-(2-氯乙基)环己-1,4-二烯甲苯 为溶剂, 反应 24.0h, 以88%的产率得到1-(2-Cyclohexa-1,4-dienyl-ethyl)-2,3-dimethyl-3H-imidazol-1-ium; chloride
    参考文献:
    名称:
    A Versatile Ruthenium Precursor for Biphasic Catalysis and Its Application in Ionic Liquid Biphasic Transfer Hydrogenation:  Conventional vs Task-Specific Catalysts
    摘要:
    The synthesis of a novel imidazolium-tagged ruthenium complex, which represents a versatile precursor for aqueous and ionic liquid biphasic catalysis, is reported. Its utility is demonstrated in the highly enantioselective ionic liquid biphasic transfer hydrogenation of acetophenone and is compared to conventional (untagged) complexes.
    DOI:
    10.1021/ja048886k
  • 作为产物:
    描述:
    1-(2'-hydroxyethyl)-1,4-cyclohexadiene四氯化碳三苯基膦 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以91%的产率得到1-(2-氯乙基)环己-1,4-二烯
    参考文献:
    名称:
    A Versatile Ruthenium Precursor for Biphasic Catalysis and Its Application in Ionic Liquid Biphasic Transfer Hydrogenation:  Conventional vs Task-Specific Catalysts
    摘要:
    The synthesis of a novel imidazolium-tagged ruthenium complex, which represents a versatile precursor for aqueous and ionic liquid biphasic catalysis, is reported. Its utility is demonstrated in the highly enantioselective ionic liquid biphasic transfer hydrogenation of acetophenone and is compared to conventional (untagged) complexes.
    DOI:
    10.1021/ja048886k
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文献信息

  • Synthesis of Imidazolium-Tethered Ruthenium(II)-Arene Complexes and Their Application in Biphasic Catalysis
    作者:Tilmann J. Geldbach、Gábor Laurenczy、Rosario Scopelliti、Paul J. Dyson
    DOI:10.1021/om050849u
    日期:2006.1.1
    Reaction of RUCl3 with 1-[2-(1,4-cyclohexadiene-1-yl)alkyl]-3-methylimidazolium chloride (alkyl = ethyl, butyl) and 1-[2-(1,4-cyclohexadiene-1-yl)ethyl]-2,3-dimethylimidazolium chloride affords a series of dimeric ruthenium complexes of the type [RuCl2(eta(6)-arene)](2)Cl-2. Treatment of these dimeric salts with phosphine ligands leads to the highly water-soluble monomeric complexes [RuCl2PR3(eta(6)-arene)]Cl (PR3 = PPh3, PCY3). Reaction of [RUCl2(eta-1-(2-benzylethyl)-3-butylimidazolium)]Cl with Ag2O gives rise to a eta(6)-arene-carbene chelate complex. The phosphine complexes have been tested as catalysts in the hydrogenation of styrene immobilized in water or an ionic liquid and in the aqueous reduction Of CO2/ CO32-. A carbonate-hydride complex has been identified as intermediate by high-pressure NMR measurements. The solid-state structures of several of the new imidazolium-functionalized arene complexes including the arene-carbene chelate complex are reported.
  • 1-vinylbenzene 1,2- and 3,4-oxides
    作者:Tadashi Watabe、Akira Hiratsuka、Toshiko Aizawa、Tadashi Sawahata
    DOI:10.1016/s0040-4039(00)87055-0
    日期:1982.1
  • WATABE TADASHI; HIRATSUKA AKIRA; AIZAWA TOSHIKO; SAWAHATA TADASHI, TETRAHEDRON LETT., 1982, 23, NO 11, 1185-1188
    作者:WATABE TADASHI、 HIRATSUKA AKIRA、 AIZAWA TOSHIKO、 SAWAHATA TADASHI
    DOI:——
    日期:——
  • A Versatile Ruthenium Precursor for Biphasic Catalysis and Its Application in Ionic Liquid Biphasic Transfer Hydrogenation:  Conventional vs Task-Specific Catalysts
    作者:Tilmann J. Geldbach、Paul J. Dyson
    DOI:10.1021/ja048886k
    日期:2004.7.1
    The synthesis of a novel imidazolium-tagged ruthenium complex, which represents a versatile precursor for aqueous and ionic liquid biphasic catalysis, is reported. Its utility is demonstrated in the highly enantioselective ionic liquid biphasic transfer hydrogenation of acetophenone and is compared to conventional (untagged) complexes.
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