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1,3-dicyclohexyl-1-tetrathiafulvalenyl-urea

中文名称
——
中文别名
——
英文名称
1,3-dicyclohexyl-1-tetrathiafulvalenyl-urea
英文别名
N-cyclohexyl-N-(cyclohexylcarbamoyl)-2-(1,3-dithiol-2-ylidene)-1,3-dithiole-4-carboxamide
1,3-dicyclohexyl-1-tetrathiafulvalenyl-urea化学式
CAS
——
化学式
C20H26N2O2S4
mdl
——
分子量
454.703
InChiKey
QXTYQFUDDBXEPC-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):
    6
  • 重原子数:
    28
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    151
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    tetrathiafulvalene-4-carboxylic acidN,N'-二环己基碳二亚胺4-二甲氨基吡啶 、 2-(6-hydroxyhexyloxy)-3-methoxy-6,7,10,11-tetrahexyloxytriphenylene 作用下, 以 四氢呋喃 为溶剂, 反应 24.0h, 以94%的产率得到1,3-dicyclohexyl-1-tetrathiafulvalenyl-urea
    参考文献:
    名称:
    Synthesis and Characterisation of Tetrathiafulvalenyl- and Ferrocenyl-Triphenylenes
    摘要:
    The synthesis, electrochemistry and mesogenic properties of novel tetrathiafulvalenyl- and ferrocenyl-triphenylenes are described. In all cases the juxtaposition of the hexa-alkyloxytriphenylene with a tetrathiafulvalene or ferrocene unit failed to give rise to derivatives displaying a discotic mesophase. Solution electrochemistry of derivatives 7 and 13 has revealed an interaction occurs between the dicationic state of the TTF moiety and the triphenylene nucleus. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(00)00250-7
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文献信息

  • Synthesis and Characterisation of Tetrathiafulvalenyl- and Ferrocenyl-Triphenylenes
    作者:Graeme Cooke、Abdulla Radhi、Neville Boden、Richard J Bushby、Zhibao Lu、Sarah Brown、Sarah L Heath
    DOI:10.1016/s0040-4020(00)00250-7
    日期:2000.5
    The synthesis, electrochemistry and mesogenic properties of novel tetrathiafulvalenyl- and ferrocenyl-triphenylenes are described. In all cases the juxtaposition of the hexa-alkyloxytriphenylene with a tetrathiafulvalene or ferrocene unit failed to give rise to derivatives displaying a discotic mesophase. Solution electrochemistry of derivatives 7 and 13 has revealed an interaction occurs between the dicationic state of the TTF moiety and the triphenylene nucleus. (C) 2000 Elsevier Science Ltd. All rights reserved.
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