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Dimethyl-tetrathiafulvalen | 54397-96-5

中文名称
——
中文别名
——
英文名称
Dimethyl-tetrathiafulvalen
英文别名
4,4'-Dimethyltetrathiafulvalene;(2Z)-4-methyl-2-(4-methyl-1,3-dithiol-2-ylidene)-1,3-dithiole
Dimethyl-tetrathiafulvalen化学式
CAS
54397-96-5
化学式
C8H8S4
mdl
——
分子量
232.416
InChiKey
KTUWYNVNQFNGBX-FPLPWBNLSA-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

物化性质

  • 沸点:
    258.1±40.0 °C(Predicted)
  • 密度:
    1.445±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    101
  • 氢给体数:
    0
  • 氢受体数:
    4

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:
    参考文献:
    名称:
    Fabre, Jean-Marc; Torreilles, Eliane; Vigroux, Michel, Journal of Chemical Research, Miniprint, 1980, # 11, p. 4572 - 4592
    摘要:
    DOI:
  • 作为产物:
    描述:
    三乙胺 作用下, 以 乙腈 为溶剂, 生成 Dimethyl-tetrathiafulvalen
    参考文献:
    名称:
    Fabre, Jean-Marc; Torreilles, Eliane; Vigroux, Michel, Journal of Chemical Research, Miniprint, 1980, # 11, p. 4572 - 4592
    摘要:
    DOI:
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文献信息

  • Bis- and tetrakis-(diphenylphosphino) tetrathiafulvalenes as precursors of redox-active organic—inorganic polymeric networks
    作者:M. Fourmigué、C.E. Uzelmeier、K. Boubekeur、S.L. Bartley、K.R. Dunbar
    DOI:10.1016/s0022-328x(96)06637-5
    日期:1997.2
    Lithiation of the (Z)-, (E)-dimethyltetrathiafulvalene mixture and subsequent reaction with ClPPh2 afford (Z)- and (E)-dimethyl-bis(diphenylphosphino)tetrathiafulvalene which are separated by fractional recrystallization. The identity of(Z)-P-2 has been ascertained by its X-ray crystal structure determination. By similar methods, tetrakis(diphenylphosphino)tetrathiafulvalene (P-4) is obtained from the tetrathiafulvalene tetralithium derivative. Cyclic voltammetry experiments reveal that the new compounds oxidize reversibly in two one-electron steps to the radical cation and dication. Reaction of o-P-2 with the dinuclear complex [Rh-2(NCCH3)(10)](BF4)(4) has been investigated and found to produce the square-planar Rh(I) compound [(o-P-2)(2)Rh][BF4]. The identity of the product has been confirmed by X-ray crystallography, FAB-MS, elemental analysis, and NMR spectroscopy. Several reactions of solvated cations were also performed, all of which appear to lead to products with o-P-2 and P-4 ligands.
  • Noncoupling synthesis of tetrathiafulvalenes
    作者:R. R. Schumaker、V. Y. Lee、E. M. Engler
    DOI:10.1021/jo00177a041
    日期:1984.2
  • POLYMER, SEMICONDUCTOR FILM, ELECTRODE, ELECTRODE ACTIVE MATERIAL, ELECTROCHEMICAL ELEMENT AND ELECTRICITY STORAGE DEVICE
    申请人:Panasonic Corporation
    公开号:EP2308912B1
    公开(公告)日:2016-01-06
  • US8481674B2
    申请人:——
    公开号:US8481674B2
    公开(公告)日:2013-07-09
  • Fabre, Jean-Marc; Torreilles, Eliane; Vigroux, Michel, Journal of Chemical Research, Miniprint, 1980, # 11, p. 4572 - 4592
    作者:Fabre, Jean-Marc、Torreilles, Eliane、Vigroux, Michel、Ciral, Louis
    DOI:——
    日期:——
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同类化合物

四硫杂富瓦烯-D4 四硫富瓦烯 四(戊硫代)四硫富瓦烯 四(十八烷基硫代)四硫富瓦烯 四(乙硫基)四硫富瓦烯[有机电子材料] 双(亚乙基二硫醇)四硫代富瓦烯 双(三亚甲基二硫代)四硫富瓦烯 [1,3]二噻唑并[4,5-d]-1,3-二噻唑,2,5-二(1,3-二硫醇-2-亚基)- 5-甲基二硫杂环戊烯-3-硫酮 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-羧酸乙酯 5-氨基-3-硫代氧基-3H-(1,2)二硫杂环戊烯-4-甲腈 5,6-二氢-4H-环戊并[1,2]二硫代-3-硫酮 4,4’,5-三甲基四硫富瓦烯 4-甲基二硫杂环戊烯-3-硫酮 4-新戊基-3H-1,2-二硫杂环戊烯-3-硫酮 4,5-二甲基-3H-1,2-二硫醇-3-酮 4,5,6,7-四氢苯并[1,2]二硫-3-硫酮 4,4’-二甲基连四硫富瓦烯 4,4,5,5,6,6,7,7-八氢二苯并四硫富瓦烯 3H-1,2-二硫杂环戊二烯-3-酮 3H-1,2-二硫杂环戊二烯-3-硫酮 2-(4,5-二甲基-1,3-二硫杂环戊烯-2-亚基)-4,5-二甲基-1,3-二硫杂环戊烯 2,3,6,7-四(2-氰乙基硫代)四硫富瓦烯 1,3-二噻唑,2-[4,5-二(癸基硫代)-1,3-二硫醇-2-亚基]-4,5-二(癸基硫代)- (四甲基硫)四硫富瓦烯 2,3,6,7-tetrakis[2-(2-methoxyethoxy)ethylsulfanyl]tetrathiafulvalene 2,3-bis[2-(2-methoxyethoxy)ethylsulfanyl]-6,7-bis(methylsulfanyl)tetrathiafulvalene (5S,6S,5'S,6'S)-5,5',6,6'-tetramethyl-bis(ethylenedithio)tetrathiafulvalene 2,5-bis(4,5-ethylenedithio-1,3-dithiol-2-ylidene)-1,3,4,6-tetrathiapentalene 2,3,6,7-Tetrakis(1-octyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-dodecyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-pentyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-hexyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-propoxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-decyloxymethyl)tetrathiafulvalene 2,3,6,7-Tetrakis(1-heptyloxymethyl)tetrathiafulvalene 2,6-bis(thioacetopentadecylamido)-3,7-bis(methylthiotetrathiafulvalene) 2,7-bis(thioacetopentadecylamido)-3,6-bis(methylthiotetrathiafulvalene) ethane 1,2-dithiol 2,3,6,7-Tetrakis(1-tetradecyloxymethyl)tetrathiafulvalene 2-Isopropyliden-1,3-dithiol-4,5-dicarbonitril 4,5-bis(butylthio)tetrathiafulvalene 2,3-dicyano-6,7-bis(butylthio)tetrathiafulvalene Tetrabutylammonium-(3-thioxo-3H-1,2-dithiol-5-thiolat) 5,6-dihydro-5-dimethoxymethyl-2-(5',6'-dihydro-1,3-dithiolo[4,5-b]-1,4-dithiin-2'-ylidene)-1,3-dithiolo[4,5-b]-1,4-dithiin 3H-1,2-dithiole 2,2'-(But-2-en-1,4-diyliden)bis[1,3-dithiol-4,5-dicarbonitril] 3-methylsulfanyl-[1,2]dithiolylium; iodide 2,2'-(Dodeca-2,4,6,8,10-pentaen-1,12-diyliden)bis[1,3-dithiol-4,5-dicarbonitril] (E,E)-1,6-bis[4,5-bis(methylsulfanyl)-1,3-dithiol-2-ylidene]hexa-2,4-diene