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4-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)vinyl)-6-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-7-yl)vinyl)thieno[3,4-d]-1,3-dithiol-2-one | 1196714-98-3

中文名称
——
中文别名
——
英文名称
4-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)vinyl)-6-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-7-yl)vinyl)thieno[3,4-d]-1,3-dithiol-2-one
英文别名
4,6-bis[(E)-2-(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)ethenyl]thieno[3,4-d][1,3]dithiol-2-one
4-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)vinyl)-6-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-7-yl)vinyl)thieno[3,4-d]-1,3-dithiol-2-one化学式
CAS
1196714-98-3
化学式
C21H14O5S5
mdl
——
分子量
506.669
InChiKey
MNCOTAGYLFMXPO-ZPUQHVIOSA-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:
    31
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    189
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    1,1'-[(4,6-thieno[3,4-d]-1,3-dithiol-2-one-diyl)bismethylene]bis[triphenylphoshonium chloride] 、 3,4-乙撑基二氧甲醛噻吩potassium tert-butylate溶剂黄146 作用下, 以 四氢呋喃氯仿 为溶剂, 以38%的产率得到4-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-5-yl)vinyl)-6-((E)-2-(2,3-dihydrothieno[3,4-b]-1,4-dioxin-7-yl)vinyl)thieno[3,4-d]-1,3-dithiol-2-one
    参考文献:
    名称:
    Synthesis of Trithienylenevinylenes Bearing Dithiocarbonate Groups and Their Dithiophene−Tetrathiafulvalene Derivatives
    摘要:
    A series of conjugated trithienylenevinylene compounds bearing dithiocarbonate groups were prepared by Wittig reactions. Dithiophene-tetrithiafulvalene (DT-TTF) derivatives can be readily prepared through trialkylphosphite-mediated coupling reactions of these trithienylenevinylene materials. All compounds were characterized by NMR, FT-IR, UV-vis, and mass spectroscopy.
    DOI:
    10.1021/jo901574v
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文献信息

  • Synthesis of Trithienylenevinylenes Bearing Dithiocarbonate Groups and Their Dithiophene−Tetrathiafulvalene Derivatives
    作者:Xin Chen、Norma R. de Tacconi、Ronald L. Elsenbaumer
    DOI:10.1021/jo901574v
    日期:2009.12.4
    A series of conjugated trithienylenevinylene compounds bearing dithiocarbonate groups were prepared by Wittig reactions. Dithiophene-tetrithiafulvalene (DT-TTF) derivatives can be readily prepared through trialkylphosphite-mediated coupling reactions of these trithienylenevinylene materials. All compounds were characterized by NMR, FT-IR, UV-vis, and mass spectroscopy.
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