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1,2,4,5-tetrakis[(4-pyridylsulfanyl)methyl]benzene

中文名称
——
中文别名
——
英文名称
1,2,4,5-tetrakis[(4-pyridylsulfanyl)methyl]benzene
英文别名
4-[[2,4,5-Tris(pyridin-4-ylsulfanylmethyl)phenyl]methylsulfanyl]pyridine;4-[[2,4,5-tris(pyridin-4-ylsulfanylmethyl)phenyl]methylsulfanyl]pyridine
1,2,4,5-tetrakis[(4-pyridylsulfanyl)methyl]benzene化学式
CAS
——
化学式
C30H26N4S4
mdl
——
分子量
570.827
InChiKey
PYTQMUQZVXSXJW-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):
    5.7
  • 重原子数:
    38
  • 可旋转键数:
    12
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    153
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    吡啶-4(1H)-硫酮四溴甲苯三乙胺 作用下, 以 乙腈 为溶剂, 以50%的产率得到1,2,4,5-tetrakis[(4-pyridylsulfanyl)methyl]benzene
    参考文献:
    名称:
    Syntheses and X-ray crystal structures of poly(pyridylsulfanylmethyl)arenes: new multi-armed molecules
    摘要:
    The synthesis of a series of seven new poly(pyridylsulfanylmethyl)arenes is reported. These are readily prepared from either 2- or 4-mercaptopyridine and a poly(bromomethyl)arene in the presence of triethylamine. Compounds with three, four, six and eight pyridylsulfanylmethyl arms are reported. These have been fully characterised and, in four cases, the relative orientations of the pyridylsulfanylmethyl arms have been ascertained by X-ray structural analysis. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(03)00550-7
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文献信息

  • Syntheses and X-ray crystal structures of poly(pyridylsulfanylmethyl)arenes: new multi-armed molecules
    作者:David A McMorran、Peter J Steel
    DOI:10.1016/s0040-4020(03)00550-7
    日期:2003.5
    The synthesis of a series of seven new poly(pyridylsulfanylmethyl)arenes is reported. These are readily prepared from either 2- or 4-mercaptopyridine and a poly(bromomethyl)arene in the presence of triethylamine. Compounds with three, four, six and eight pyridylsulfanylmethyl arms are reported. These have been fully characterised and, in four cases, the relative orientations of the pyridylsulfanylmethyl arms have been ascertained by X-ray structural analysis. (C) 2003 Elsevier Science Ltd. All rights reserved.
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