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1,4-Bis[[4-(4-methylphenyl)sulfanylphenyl]sulfanyl]benzene | 1151766-62-9

中文名称
——
中文别名
——
英文名称
1,4-Bis[[4-(4-methylphenyl)sulfanylphenyl]sulfanyl]benzene
英文别名
1,4-bis[[4-(4-methylphenyl)sulfanylphenyl]sulfanyl]benzene
1,4-Bis[[4-(4-methylphenyl)sulfanylphenyl]sulfanyl]benzene化学式
CAS
1151766-62-9
化学式
C32H26S4
mdl
——
分子量
538.822
InChiKey
VSUFPPHKUGRMOH-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):
    10.9
  • 重原子数:
    36
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    101
  • 氢给体数:
    0
  • 氢受体数:
    4

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

  • 作为产物:
    描述:
    1,4-bis((4-bromophenyl)thio)benzene4-甲苯硫酚吡啶喹啉copper(I) oxide 作用下, 反应 24.0h, 以5%的产率得到1,4-Bis[[4-(4-methylphenyl)sulfanylphenyl]sulfanyl]benzene
    参考文献:
    名称:
    p-Phenylene sulfide oligomers and their properties. Ar–S couplings mediated by copper or by fluorine substitutions
    摘要:
    A series of monodisperse p-phenylene sulfide oligomers were efficiently synthesized by using a bidirectional growth. A strategy combining Cu-catalyzed Ar-S couplings for small oligomers and fluorine aromatic substitutions by aryl thiolates for longer ones was put forward. The latter method is Superior to Cu-catalyzed reactions for longer oligomers. Fluorine chemistry brings some new advantages Such as solubility and reactivity, Qualitative crystallinity studies were reported according to the oligomer size and the functional series, by using a microscope equipped with a heating stage and a camera. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.02.068
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文献信息

  • p-Phenylene sulfide oligomers and their properties. Ar–S couplings mediated by copper or by fluorine substitutions
    作者:Olivier Goyot、Marc Gingras
    DOI:10.1016/j.tetlet.2009.02.068
    日期:2009.4
    A series of monodisperse p-phenylene sulfide oligomers were efficiently synthesized by using a bidirectional growth. A strategy combining Cu-catalyzed Ar-S couplings for small oligomers and fluorine aromatic substitutions by aryl thiolates for longer ones was put forward. The latter method is Superior to Cu-catalyzed reactions for longer oligomers. Fluorine chemistry brings some new advantages Such as solubility and reactivity, Qualitative crystallinity studies were reported according to the oligomer size and the functional series, by using a microscope equipped with a heating stage and a camera. (C) 2009 Elsevier Ltd. All rights reserved.
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