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[2-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]methanamine | 690253-15-7

中文名称
——
中文别名
——
英文名称
[2-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]methanamine
英文别名
[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]methanamine
[2-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]methanamine化学式
CAS
690253-15-7
化学式
C11H11NS8
mdl
——
分子量
413.743
InChiKey
RSEYNDXYBXTPFG-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):
    4.1
  • 重原子数:
    20
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    228
  • 氢给体数:
    1
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    异烟酸[2-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]methanamine对甲苯磺酰氯 作用下, 以 吡啶 为溶剂, 以80%的产率得到N-[[2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]methyl]pyridine-4-carboxamide
    参考文献:
    名称:
    Synthesis and reactivity of amino-substituted BEDT-TTF donors as building blocks for bifunctional materials
    摘要:
    The first two amino-substituted BEDT-TTF derivatives. aminomethyl-ET (AMET) and aminoethyl-ET (AEET), have been prepared; the critical step in both cases was a hetero Diels-Alder reaction with 1,3-dithiole-2,4,5-trithione. AEET shows expected reactivity towards electrophiles whereas AM ET will not react with aryl acid chlorides or sulfonyl chlorides, but amides of AMET can be produced by DCC Coupling and mixed anhydride methods. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.02.016
  • 作为产物:
    描述:
    C-(5,6,5',6'-Tetrahydro-[2,2']bi[[1,3]dithiolo[4,5-b][1,4]dithiinylidene]-5-yl)-methylamine; compound with trifluoro-acetic acid 在 sodium hydroxide 作用下, 以 四氢呋喃 为溶剂, 以100%的产率得到[2-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-5-yl]methanamine
    参考文献:
    名称:
    Synthesis and reactivity of amino-substituted BEDT-TTF donors as building blocks for bifunctional materials
    摘要:
    The first two amino-substituted BEDT-TTF derivatives. aminomethyl-ET (AMET) and aminoethyl-ET (AEET), have been prepared; the critical step in both cases was a hetero Diels-Alder reaction with 1,3-dithiole-2,4,5-trithione. AEET shows expected reactivity towards electrophiles whereas AM ET will not react with aryl acid chlorides or sulfonyl chlorides, but amides of AMET can be produced by DCC Coupling and mixed anhydride methods. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.02.016
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文献信息

  • Synthesis and reactivity of amino-substituted BEDT-TTF donors as building blocks for bifunctional materials
    作者:Jon-Paul Griffiths、Anna A. Arola、Glynn Appleby、John D. Wallis
    DOI:10.1016/j.tetlet.2004.02.016
    日期:2004.3
    The first two amino-substituted BEDT-TTF derivatives. aminomethyl-ET (AMET) and aminoethyl-ET (AEET), have been prepared; the critical step in both cases was a hetero Diels-Alder reaction with 1,3-dithiole-2,4,5-trithione. AEET shows expected reactivity towards electrophiles whereas AM ET will not react with aryl acid chlorides or sulfonyl chlorides, but amides of AMET can be produced by DCC Coupling and mixed anhydride methods. (C) 2004 Elsevier Ltd. All rights reserved.
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