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4,4',6,6'-tetra(diethoxyphosphorylmethyl)-2-(thieno[3,4-d]-1,3-dithiol-2-ylidene)thieno[3,4-d]-1,3-dithiole | 1173657-66-3

中文名称
——
中文别名
——
英文名称
4,4',6,6'-tetra(diethoxyphosphorylmethyl)-2-(thieno[3,4-d]-1,3-dithiol-2-ylidene)thieno[3,4-d]-1,3-dithiole
英文别名
2-[4,6-Bis[[diethoxy(oxido)phosphaniumyl]methyl]thieno[3,4-d][1,3]dithiol-2-ylidene]-4,6-bis[[diethoxy(oxido)phosphaniumyl]methyl]thieno[3,4-d][1,3]dithiole;2-[4,6-bis[[diethoxy(oxido)phosphaniumyl]methyl]thieno[3,4-d][1,3]dithiol-2-ylidene]-4,6-bis[[diethoxy(oxido)phosphaniumyl]methyl]thieno[3,4-d][1,3]dithiole
4,4',6,6'-tetra(diethoxyphosphorylmethyl)-2-(thieno[3,4-d]-1,3-dithiol-2-ylidene)thieno[3,4-d]-1,3-dithiole化学式
CAS
1173657-66-3
化学式
C30H48O12P4S6
mdl
——
分子量
916.995
InChiKey
ZLPBKNBBGPHADS-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
  • 重原子数:
    52
  • 可旋转键数:
    24
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    324
  • 氢给体数:
    0
  • 氢受体数:
    18

反应信息

  • 作为产物:
    描述:
    4,6-bis(chloromethyl)thieno[3,4-d]-1,3-dithiol-2-one亚磷酸三乙酯 反应 4.0h, 以32%的产率得到4,4',6,6'-tetra(diethoxyphosphorylmethyl)-2-(thieno[3,4-d]-1,3-dithiol-2-ylidene)thieno[3,4-d]-1,3-dithiole
    参考文献:
    名称:
    Synthesis of thieno[3,4-d]-1,3-dithiol-2-one derivatives
    摘要:
    A series of mono-substituted and bis-substituted derivatives of thieno [3,4-d]-1,3-dithiol-2-one were prepared through halogenation, chloromethylation, and subsequent nucleophilic substitution reactions. Compounds were characterized by NMR, FT-IR, and HRMS. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.03.225
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文献信息

  • Synthesis of thieno[3,4-d]-1,3-dithiol-2-one derivatives
    作者:Xin Chen、Ronald L. Elsenbaumer
    DOI:10.1016/j.tetlet.2009.03.225
    日期:2009.7
    A series of mono-substituted and bis-substituted derivatives of thieno [3,4-d]-1,3-dithiol-2-one were prepared through halogenation, chloromethylation, and subsequent nucleophilic substitution reactions. Compounds were characterized by NMR, FT-IR, and HRMS. (C) 2009 Elsevier Ltd. All rights reserved.
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