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vinylenedithiotetrathiafulvalene | 118148-32-6

中文名称
——
中文别名
——
英文名称
vinylenedithiotetrathiafulvalene
英文别名
2-[1,3]dithiol-2-ylidene-[1,3]dithiolo[4,5-b][1,4]dithiine;1,3-Dithiolo[4,5-b][1,4]dithiin, 2-(1,3-dithiol-2-ylidene)-;2-(1,3-dithiol-2-ylidene)-[1,3]dithiolo[4,5-b][1,4]dithiine
vinylenedithiotetrathiafulvalene化学式
CAS
118148-32-6
化学式
C8H4S6
mdl
——
分子量
292.516
InChiKey
COMIIMNCMGOMMB-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):
    3.7
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    152
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

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文献信息

  • Electrophilic halogenation of thioethers: 5-chloro- and 5,6-dichloro-5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dithiine-2-one and an efficient synthesis of vinylenedithiotetrathiafulvalene (VDT-TTF)
    作者:Olivier J. Dautel、Jan Larsen、Marc Fourmigué
    DOI:10.1039/b001996h
    日期:——
    The SO2Cl2 chlorination of 5,6-dihydro-1,3-dithiolo[4,5-b]- [1,4]dithiine-2-one affords the corresponding mono- and trans-di-chloro derivatives which eliminate HCl upon treatment with KF/18-crown-6 or LiBr/HMPA, offering an easy route to the unsaturated vinylenedithiotetrathiafulvalene (VDT-TTF).
    5,6-二氢-1,3-二戊环[4,5-b]- [1,4]二环戊烯-2-酮的SO2Cl2化反应可得到相应的单和反式二生物,这些衍生物在用KF/18-冠-6或LiBr/HMPA处理时可消除HCl,从而为不饱和乙烯基四硫富瓦烯(VDT-TTF)提供了一条简单途径。
  • PAPAVASSILIOU, G. C.;MOUSDIS, G. A.;YIANNOPOULOS, S. Y.;KAKOUSSIS, V. C.;+, SYNTH. MET., 27,(1988) N-4, C. B373-B378
    作者:PAPAVASSILIOU, G. C.、MOUSDIS, G. A.、YIANNOPOULOS, S. Y.、KAKOUSSIS, V. C.、+
    DOI:——
    日期:——
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同类化合物

提亚鲁布林A 乙烯基 3-硝基-2,5-二苯基-1,4-二噻英 3,6-二苯基二噻英 2-溴-5-硝基-3,6-二苯基-1,4-二噻英 2-乙烯基-4H-1,3-二噻英 2-[4-(6-丙-1-炔基二噻英-3-基)丁-1,3-二炔基]环氧乙烷 2,5-二苯基-1,4-二噻英 2,5-二溴-3,6-二苯基-1,4-二噻英 2,3-二硫杂二环[2.2.2]辛-5-烯 2,3,5,6-四氰基-[1,4]-二噻硫 1,2-二硫杂-4,5-二甲基-4-环己烯 1,2-二噻英-3,6-二胺 [1,4]dithiin-1,4-dioxide 3,6-dihydro-3-methyl-1,2-dithiin (+/-)-diborn-2-eno<2,3-c;3',2'-e><1,2>dithiine 4,5-dimethyl-3H,6H-1,2-dithiin 1-oxide 3,6-bis<(isobutyryloxy)methyl>-1,2-dithiin 3,6-bis<<(cyclopropylcarbonyl)oxy>methyl>-1,2-dithiin 3-<<(cyclopentylcarbonyl)oxy>methyl>-6-(hydroxymethyl)-1,2-dithiin 3-<(acetyloxy)methyl>-6-(hydroxymethyl)-1,2-dithiin 3-<<(cyclopropylcarbonyl)oxy>methyl>-6-(hydroxymethyl)-1,2-dithiin 3,6-bis<<(cyclopentylcarbonyl)oxy>methyl>-1,2-dithiin 3,6-bis(formyl)-1,2-dithiin 3,6-bis<(acetyloxy)methyl>-1,2-dithiin 2-(2'-<3',4'-dihydro-2H-thiopyranyl>)-4H-<1,3>-dithiin 3,6-bis<(propionyloxy)methyl>-1,2-dithiin 1,2,4,5-Benzotetrathiole 1-Methyl-2,5-diphenyl-1,4-dithiin-1-ium tetrafluoroborate vinylenedithiotetrathiafulvalene 2,3,5,6-Tetramethyl-[1,4]dithiine 2,5-Diphenyl-6-bromo-3-nitro-1,4-dithiin-4-sulphoxide 3,6-Bis-(4-butyl-phenyl)-[1,2]dithiine 1,4-Dithiin-tetracarboxamid 3,6-bis(trimethylsilyl)-1,2-dithiin 3,6-di[2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl]oxymethyl-1,2-dithiin 1,2,3,4,6,7,8,9-Octahydro-thianthrene ((2S,4S)-pentane-2,4-dithio)((1'R,5'R)-6',6'-dimethyl-bicyclo[3.1.1]heptene-2',3'-dithio)tetrathiafulvalene (ethylenedithio)((1R,5R)-6,6-dimethyl-bicyclo[3.1.1]heptene-2,3-dithio)tetrathiafulvalene octafluoro-2,7-dithiatricyclo<6.2.0.03,6>deca-1(8),3(6)-diene 2,5-Dimethyl-3,6-diphenyl-[1,4]dithiin 2,5-Di(t-butyl)-1,4-dithiin 2,6-di(2-thienyl)-1,4-dithiin 3,6-bis(tert-butyl)-1,2-dithiin 2,3-(2,3-dithiabutane-1,4-diyl)-6,7-bis(methylsulfanyl)tetrathiafulvalene 4-methyl-2-propenyl-4H-1,3-dithiin 2,3-dithiabicyclo<2.2.1>hept-5-ene 2,3-Bis(2-cyanoethylthio)-6,7-bis(2,3-dithiabutane-1,4-diyl)tetrathiafulvalene 3-(Acetamido)methyl-6-[(tert-butyldimethylsilyloxy)methyl]-1,2-dithiin 3-<<(tert-butyldimethylsilyl)oxy>methyl>-6-(2-cyanoethen-1-yl)-1,2-dithiin