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25,27-Bis(3-bromopropoxy)-5,11,17,23-tetratert-butyl-26,28-dimethoxy-2,8,14,20-tetrathiapentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3,5,7(28),9,11,13(27),15(26),16,18,21(25),22-dodecaene | 1042437-47-7

中文名称
——
中文别名
——
英文名称
25,27-Bis(3-bromopropoxy)-5,11,17,23-tetratert-butyl-26,28-dimethoxy-2,8,14,20-tetrathiapentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3,5,7(28),9,11,13(27),15(26),16,18,21(25),22-dodecaene
英文别名
25,27-bis(3-bromopropoxy)-5,11,17,23-tetratert-butyl-26,28-dimethoxy-2,8,14,20-tetrathiapentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3,5,7(28),9,11,13(27),15(26),16,18,21(25),22-dodecaene
25,27-Bis(3-bromopropoxy)-5,11,17,23-tetratert-butyl-26,28-dimethoxy-2,8,14,20-tetrathiapentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3,5,7(28),9,11,13(27),15(26),16,18,21(25),22-dodecaene化学式
CAS
1042437-47-7
化学式
C48H62Br2O4S4
mdl
——
分子量
991.09
InChiKey
KHFBZPXOWNQPMV-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):
    17.1
  • 重原子数:
    58
  • 可旋转键数:
    14
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    138
  • 氢给体数:
    0
  • 氢受体数:
    8

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

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文献信息

  • Synthesis, Structure and Electrochemical Behavior of a Novel Redox-Active Thiacalix[4]arene-Tetrathiafulvalene Assembly
    作者:Bang-Tun Zhao、Wen-Bo Guo、Pu-Zhou Hu
    DOI:10.3987/com-10-11965
    日期:——
    A novel redox-active thiacalix[4]arene-tetrathiafulvalene assembly 5 was carried out through triethyl phosphite-mediated cross-coupling of the corresponding two 1,3-dithiole-2-(thi)ones (3 and 4). The structure of thiacalix[4]arene-tetrathiafulvalene assembly 5 was identified by X-ray diffraction analysis. Meanwhile, the preliminary electrochemical properties of 5 was investigated by cyclic voltammetry (CV) and two one-electron quasi-reversible waves with redox potentials are observed.
  • Synthesis and electrochemical behavior of a model redox-active thiacalix[4]arene-tetrathiafulvalene assembly
    作者:Bang-Tun Zhao、Zhen Zhou、Zhen-Ning Yan、Esmah Belhadj、Franck Le Derf、Marc Sallé
    DOI:10.1016/j.tetlet.2010.08.116
    日期:2010.11
    Syntheses of the first bisthiacalix[4]arenes systems bridged by a tetrathiafulvalene (TTF) framework have been carried out through triethyl phosphite-mediated dechalcogenation dimerization of the corresponding 1,3-dithiole-2-ones. The cyclic voltammograms of the resulting bisthiacalix[4]arenes tethered by an electroactive TTF unit are provided, and exhibit an electrochemical response in the case of
    通过四硫富瓦烯(TTF)骨架桥接的第一个bisthiacalix [4]芳烃体系的合成已通过亚磷酸三乙酯介导的相应的1,3-二硫代-2-酮的脱硫二聚作用进行。提供了由电活性TTF单元束缚的生成的bisthiacalix [4]芳烃的循环伏安图,在引入Ag +的情况下,表现出电化学响应。
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