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4-(2-cyanoethylthio)-5-methoxycarbonyl-1,3-dithiol-2-one | 191932-41-9

中文名称
——
中文别名
——
英文名称
4-(2-cyanoethylthio)-5-methoxycarbonyl-1,3-dithiol-2-one
英文别名
Methyl 5-(2-cyanoethylsulfanyl)-2-oxo-1,3-dithiole-4-carboxylate
4-(2-cyanoethylthio)-5-methoxycarbonyl-1,3-dithiol-2-one化学式
CAS
191932-41-9
化学式
C8H7NO3S3
mdl
——
分子量
261.346
InChiKey
CHCATQSBRVLIBB-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):
    1.8
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    143
  • 氢给体数:
    0
  • 氢受体数:
    7

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

  • 作为反应物:
    描述:
    4-(2-cyanoethylthio)-5-methoxycarbonyl-1,3-dithiol-2-one亚磷酸三乙酯 作用下, 以 为溶剂, 反应 20.0h, 以72%的产率得到2,6(7)-bis[(2-cyanoethyl)thio]-3,7(6)-bis(methoxycarbonyl)tetrathiafulvalene
    参考文献:
    名称:
    Geometrically Constrained Tetrathiafulvalenophanes:  Synthesis and Characterization
    摘要:
    The synthesis of tetrathiafulvalenophanes 4b, 4c, 5, 9, and 10 employing two fundamentally different strategies is reported. Macrocycle 9 was obtained as a mixture of cis and trans isomers and was crystallized to afford two distinct crystals types: a red type consisting of the cis isomer and a yellow type consisting of the trans isomer. The crystal structures of cis-9 and trans-9, determined by X-ray diffraction, revealed that the cis-form possesses a planar TTF moiety while the trans-form has a distorted TTF unit. The electrochemical properties of the new tetrathiafulvalenophanes are reported.
    DOI:
    10.1021/jo970326z
  • 作为产物:
    描述:
    4-<(2-cyanoethyl)thio>-5-(methoxycarbonyl)-1,3-dithiole-2-thionemercury(II) diacetate 作用下, 以 氯仿溶剂黄146 为溶剂, 反应 2.0h, 以86%的产率得到4-(2-cyanoethylthio)-5-methoxycarbonyl-1,3-dithiol-2-one
    参考文献:
    名称:
    Geometrically Constrained Tetrathiafulvalenophanes:  Synthesis and Characterization
    摘要:
    The synthesis of tetrathiafulvalenophanes 4b, 4c, 5, 9, and 10 employing two fundamentally different strategies is reported. Macrocycle 9 was obtained as a mixture of cis and trans isomers and was crystallized to afford two distinct crystals types: a red type consisting of the cis isomer and a yellow type consisting of the trans isomer. The crystal structures of cis-9 and trans-9, determined by X-ray diffraction, revealed that the cis-form possesses a planar TTF moiety while the trans-form has a distorted TTF unit. The electrochemical properties of the new tetrathiafulvalenophanes are reported.
    DOI:
    10.1021/jo970326z
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文献信息

  • Synthesis of linear oligo-TTFs and their [2]rotaxanes with cyclobis(paraquat-p-phenylene)
    作者:Dorthe Damgaard、Mogens Brøndsted Nielsen、Jesper Lau、Kenneth Bendix Jensen、Roman Zubarev、Eric Levillain、Jan Becher
    DOI:10.1039/b001868f
    日期:——
    Two linear oligo-TTFs were synthesised employing a stepwise strategy involving two different thiolate protecting groups. These linear TTFs were incorporated into donor–acceptor rotaxanes with the cyclic acceptor, cyclobis(paraquat-p-phenylene). Moreover, a prototype rotaxane based on a bis(pyrrolo)-TTF was prepared and studied.
    采用涉及两种不同硫醇酯保护基团的分步策略,合成了两种线性寡 TTF。这些线性 TTF 与环状受体环双(百草枯对苯二甲酸酯)结合成了供体-受体轮烷。此外,还制备并研究了一种基于双(吡咯)-TTF 的轮烷原型。
  • Geometrically Constrained Tetrathiafulvalenophanes:  Synthesis and Characterization
    作者:Jesper Lau、Philippe Blanchard、Amédée Riou、Michel Jubault、Michael P. Cava、Jan Becher
    DOI:10.1021/jo970326z
    日期:1997.7.1
    The synthesis of tetrathiafulvalenophanes 4b, 4c, 5, 9, and 10 employing two fundamentally different strategies is reported. Macrocycle 9 was obtained as a mixture of cis and trans isomers and was crystallized to afford two distinct crystals types: a red type consisting of the cis isomer and a yellow type consisting of the trans isomer. The crystal structures of cis-9 and trans-9, determined by X-ray diffraction, revealed that the cis-form possesses a planar TTF moiety while the trans-form has a distorted TTF unit. The electrochemical properties of the new tetrathiafulvalenophanes are reported.
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