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4-fluorocarbonyltetrathiafulvalene | 255870-35-0

中文名称
——
中文别名
——
英文名称
4-fluorocarbonyltetrathiafulvalene
英文别名
2-(1,3-Dithiol-2-ylidene)-1,3-dithiole-4-carbonyl fluoride
4-fluorocarbonyltetrathiafulvalene化学式
CAS
255870-35-0
化学式
C7H3FOS4
mdl
——
分子量
250.363
InChiKey
YUQQXBDFWJRMDA-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

物化性质

  • 沸点:
    270.9±40.0 °C(Predicted)
  • 密度:
    1.750±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    118
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    1-十六烷醇4-fluorocarbonyltetrathiafulvalene4-二甲氨基吡啶 作用下, 以 二氯甲烷 为溶剂, 反应 12.0h, 以93%的产率得到[2,2']Bi[[1,3]dithiolylidene]-4-carboxylic acid hexadecyl ester
    参考文献:
    名称:
    Fluorocarbonyltetrathiafulvalene: an effective building block for the production of tetrathiafulvalene esters and amides
    摘要:
    4-Fluorocarbonyltetrathiafulvalene has been synthesised under mild conditions, and has been reacted with alcohols and amides to furnish esters and amides in near quantitative yield. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(99)01804-3
  • 作为产物:
    描述:
    tetrathiafulvalene-4-carboxylic acid吡啶三聚氟氰 作用下, 以 二氯甲烷 为溶剂, 反应 1.5h, 以83%的产率得到4-fluorocarbonyltetrathiafulvalene
    参考文献:
    名称:
    Fluorocarbonyltetrathiafulvalene: an effective building block for the production of tetrathiafulvalene esters and amides
    摘要:
    4-Fluorocarbonyltetrathiafulvalene has been synthesised under mild conditions, and has been reacted with alcohols and amides to furnish esters and amides in near quantitative yield. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(99)01804-3
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文献信息

  • Synthesis and Characterisation of Tetrathiafulvalenyl- and Ferrocenyl-Triphenylenes
    作者:Graeme Cooke、Abdulla Radhi、Neville Boden、Richard J Bushby、Zhibao Lu、Sarah Brown、Sarah L Heath
    DOI:10.1016/s0040-4020(00)00250-7
    日期:2000.5
    The synthesis, electrochemistry and mesogenic properties of novel tetrathiafulvalenyl- and ferrocenyl-triphenylenes are described. In all cases the juxtaposition of the hexa-alkyloxytriphenylene with a tetrathiafulvalene or ferrocene unit failed to give rise to derivatives displaying a discotic mesophase. Solution electrochemistry of derivatives 7 and 13 has revealed an interaction occurs between the dicationic state of the TTF moiety and the triphenylene nucleus. (C) 2000 Elsevier Science Ltd. All rights reserved.
  • An electrochemically tuneable cyclodextrin-based molecular adapter
    作者:Graeme Cooke、Patrice Woisel、François Delattre、Marc Bria、James F. Garety、Shanika Gunatiliaka Hewage、Gouher Rabani
    DOI:10.1016/j.tetlet.2006.06.116
    日期:2006.9
    We report the synthesis of a cyclodextrin-based molecular adapter which has the propensity to form an electrochemically tuneable ternary complex with cyclophanes 2 or 3 and ferrocene 4 in non-aqueous and aqueous environments, respectively. (c) 2006 Elsevier Ltd. All rights reserved.
  • Fluorocarbonyltetrathiafulvalene: an effective building block for the production of tetrathiafulvalene esters and amides
    作者:Graeme Cooke、Vincent M. Rotello、Abdulla Radhi
    DOI:10.1016/s0040-4039(99)01804-3
    日期:1999.12
    4-Fluorocarbonyltetrathiafulvalene has been synthesised under mild conditions, and has been reacted with alcohols and amides to furnish esters and amides in near quantitative yield. (C) 1999 Elsevier Science Ltd. All rights reserved.
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同类化合物

甲酰四硫富瓦烯 环己酮,2-[二(甲硫基)亚甲基]- 5-乙基-2-甲基-噻吩-3-酮 4-羟基-2,5-二甲基噻吩-3(2H)-酮 4-乙基硫烷基-丁-3-烯-2-酮 4,4-二甲基-1,1-双(甲基硫代)-1-戊烯-3-酮 3-[双(甲基磺酰基)亚甲基]-2,4-戊二酮 3,3-双(甲硫基)-2-氰基丙烯酸乙酯 2-氰基-3,3-双(甲基硫代)丙烯酰胺 2-氰-3,3-二(甲硫基)丙烯酸甲酯 2-氯-3-氧代-2,3-二氢-2-噻吩羧酸甲酯 2-氨基-4,5-二氢-3-噻吩甲酰胺 2-乙酰基-3-氨基-3-甲基硫代丙烯腈 2-丙烯酸,3-(十六烷基硫代)-,甲基酯,(Z)- 2-(环丙基羰基)-3,3-二(甲基硫代)丙烯腈 2-(1,3-二噻戊环-2-亚基)环戊酮 2-(1,3-二噻戊环-2-亚基)环己酮 2,2-二甲基噻吩-3-酮 1-己烯-3-酮,1,1-二(甲硫基)-2-硝基- 1,3-二硫杂环戊烯-4-羧酸 (3Z)-1,1,1-三氟-4-(甲硫基)-3-丁烯-2-酮 (3E)-4-(甲硫基)-3-戊烯-2-酮 (2Z)-[3-(2-溴乙基)-4-氧代-1,3-噻唑烷-2-亚基]乙酸乙酯 (2Z)-2-(3-乙基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2Z)-(3-甲基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2E)-2-(4-氧代噻唑烷-2-亚基)乙酸丁酯 2-[bis(methylthio)methylene]-5-([13C]-methyl)cyclohexanone 2-Cyan-2-(2,3,4,5,6,7-hexahydrobenzothiazol-2-yliden)essigsaeuremethylester 2-(chlorodifluoromethylcarbonylmethylene)-1,3-thiazolidine 2,3-bis((S)-2-dodecyloxy-propanylthio)-6-(carboxy)tetrathiafulvalene 3-Amino-2-cyan-3-(ethylthio)acrylsaeuremethylester 5-dimethylaminomethylene-3-ethoxycarbonyl-2-methyl-4-oxo-4,5-dihydrothiophene 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-dithiolane 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-oxathiolane (Z)-4-(1-Butylthio)-but-3-en-2-one methyl 3-(butylthio)acrylate 3-Methylamino-3-methylmercapto-2-cyan-acrylsaeure-methylester 2-sec-butoxy-3,5-dimethylthiotetronic acid ethyl 2-amino-4-hydroxy-5-methyl-4-(trifluoromethyl)-4,5-dihydrothiophene-3-carboxylate cyano-(3-ethyl-4-oxo-thiazolidin-2-yliden)-acetic acid allyl ester 2‑(3,3‑dimethyl‑2‑oxobutylidene)‑1,3‑thiazolidin‑4‑one isopropyl 1,3-dithiol-2-ylidenemethylsulfonylacetate (E)-5-(furan-2-yl)-1,1-bis(methylthio)penta-1,4-dien-3-one ethyl 3-cyclohexylamino-3-methylthio-2-cyanoacrylate ethyl 2-ethoxy-4,5-dihydrothiophene-3-carboxylate 2,4-dimethyl-2,3-dihydro-thiophen-3-one isopropyl 2-(1,3-dithiol-2-ylidene)-2-(N-cyclohexylcarbamoyl)acetate 4,4-bis(methylthio)but-3-en-2-one-1,1,1,3-d4 N-(2-aminoethyl)-benzo[b]thieno[2,3-c]pyridine-3-carboamide.hydrochloride 3-(1,3-dithiolan-2-ylidene)butan-2-one