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4-Bromotetrafluorothiophenol | 173441-75-3

中文名称
——
中文别名
——
英文名称
4-Bromotetrafluorothiophenol
英文别名
4-bromotetrafluorobenzenethiol;4-bromo-2,3,5,6-tetrafluorobenzenethiol;4-Bromo-2,3,5,6-tetrafluorobenzene-thiol
4-Bromotetrafluorothiophenol化学式
CAS
173441-75-3
化学式
C6HBrF4S
mdl
——
分子量
261.038
InChiKey
TUOPQRPSDZNMBQ-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:
    203.6±35.0 °C(Predicted)
  • 密度:
    1.932±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    1
  • 氢给体数:
    1
  • 氢受体数:
    5

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-Bromotetrafluorothiophenol硝酸 作用下, 反应 8.12h, 生成 Perfluoro-2,3-dihydrobenzothiophene-1-oxide
    参考文献:
    名称:
    含氟有机硫的化合物。二。全氟-2,3-二氢苯并[ b ]噻吩的合成及其某些化学性质的研究
    摘要:
    全氟-2,3-二氢苯并[ b ]噻吩(I)和一些全氟茚满,是通过在碘存在下,将许多4-取代的四氟噻吩酚与四氟乙烯进行共水解而获得的。已经研究了硫化物I与某些亲核试剂和氧化剂的相互作用。已经合成了多氟-2,3-二氢苯并噻吩的5-和6-取代的衍生物。
    DOI:
    10.1016/0022-1139(95)03294-n
  • 作为产物:
    描述:
    溴五氟苯吡啶potassium hydrosulfide 作用下, 以 乙二醇 为溶剂, 反应 0.25h, 生成 4-Bromotetrafluorothiophenol
    参考文献:
    名称:
    含氟有机硫的化合物。二。全氟-2,3-二氢苯并[ b ]噻吩的合成及其某些化学性质的研究
    摘要:
    全氟-2,3-二氢苯并[ b ]噻吩(I)和一些全氟茚满,是通过在碘存在下,将许多4-取代的四氟噻吩酚与四氟乙烯进行共水解而获得的。已经研究了硫化物I与某些亲核试剂和氧化剂的相互作用。已经合成了多氟-2,3-二氢苯并噻吩的5-和6-取代的衍生物。
    DOI:
    10.1016/0022-1139(95)03294-n
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文献信息

  • Cu(I)/Chiral Bisoxazoline‐Catalyzed Enantioselective Doyle‐Kirmse Reaction of Allenyl Sulfides with <i>α</i> ‐Diazoesters
    作者:Kang Wang、Shu‐Sen Li、Jianbo Wang
    DOI:10.1002/chem.202200170
    日期:2022.4.12
    A Cu(I)/chiral bisoxazoline-catalyzed enantioselective Doyle-Kirmse reaction of polyfluoroaryl allenyl sulfides with α-diazoesters, generating chiral tertiary homopropargylic sulfides in good enantioselectivities under mild conditions.
    Cu(I)/手性双恶唑啉催化的多氟芳基烯基硫化物与α-重氮酯的对映选择性 Doyle-Kirmse 反应,在温和条件下生成具有良好对映选择性的手性叔丙炔丙基硫化物。
  • METHOD FOR PRODUCING STRUCTURE WHEREIN AROMATIC POLYMER IS BONDED TO BASE, STRUCTURE HAVING AROMATIC POLYMER CHAIN BONDED TO CONDUCTIVE BASE, AND ELECTRONIC DEVICE COMPRISING THE STRUCTURE
    申请人:Tanaka Kenta
    公开号:US20100069603A1
    公开(公告)日:2010-03-18
    Disclosed is a method for efficiently producing a structure wherein an aromatic polymer is bonded to a base. Also disclosed is such a structure wherein the base is electrically conductive. Specifically disclosed is a method for producing a structure, which comprises a step for polycondensing an aromatic compound represented by the formula (I) below in the presence of a polymerization catalyst and a base having a group represented by the formula (II) below. MY n Ar—X  (I) (In the formula (I), Ar represents a divalent group composed of an aromatic ring; X represents a halogen atom or the like; Y represents an oxygen atom, a sulfur atom, an imino group or the like; n represents 0 or 1; and M represents a hydrogen atom, —B(OQ 1 ) 2 (wherein Q 1 represents a hydrogen atom, a hydrocarbon group or the like) or the like.) —Ar a —(X a ) p (II) (In the formula (II), Ar a represents a group having a valence of (p+1) and composed of an aromatic ring; X a represents a halogen atom or a monovalent group expressed as —SO 3 Q a (wherein Q a represents a substituted or unsubstituted hydrocarbon group); p represents an integer not less than 1, and when p is an integer not less than 2, the plurality of X a 's may be the same as or different from each other.)
    公开了一种高效生产芳香族聚合物与基体结合的结构的方法。还公开了这样一种结构,其中基体具有电导性。具体公开了一种生产结构的方法,该方法包括在聚合催化剂和具有以下式子(II)中表示的基团的碱存在下,聚合表示为以下式子(I)的芳香族化合物的步骤。MYnAr—X  (I)(在式(I)中,Ar表示由芳香族环组成的二价基团;X表示卤素原子或类似物;Y表示氧原子、硫原子、亚胺基或类似物;n表示0或1;M表示氢原子,-B(OQ1)2(其中Q1表示氢原子、碳氢基团或类似物)或类似物。)—Ara—(Xa)p(II)(在式(II)中,Ararepresents具有(p+1)价且由芳香族环组成的基团;Xarepresents卤素原子或表示为-SO3Qa的一价基团(其中Qarepresents取代或未取代的碳氢基团);p表示不小于1的整数,当p为不小于2的整数时,Xa的多个可以相同也可以不同。)
  • Synthesis of chloropolyfluoroarenes from polyfluoroarenethiols and PCl5
    作者:P. V. Nikul’shin、А. M. Maksimov、V. Е. Platonov
    DOI:10.1134/s1070428016020068
    日期:2016.2
    Replacement of the thiol group in polyfluoroarenethiols with chlorine was performed by treating with PCl5 as chlorinating agent. By heating in ampules at 200-220A degrees C polyfluoro- and polyfluorochloroarenethiols with PCl5 mono- and dichloropolyfluoroarenes and also 1,2,4-trifluorotrichlorobenzene were synthesized. Dichloropolyfluoroarenes contain chlorine atoms in ortho- and para-positions.
  • Reaction of polyfluoroarenesulfonyl bromides with allyl bromide. Synthesis of allyl polyfluoroaryl sulfones
    作者:R. A. Bredikhin、A. M. Maksimov、V. E. Platonov
    DOI:10.1134/s1070428011030080
    日期:2011.3
    Reactions of polyfluoroarenesulfonyl bromides 4-XC6F4SO2Br (X = F, H, Cl, Br, CF3) with allyl bromide gave 84-94% of the corresponding allyl polyfluoroaryl sulfones.
  • Fluoroorganic sulphur-containing compounds. II. The synthesis of perfluoro-2,3-dihydrobenzo[b]thiophene and an investigation of some of its chemical properties
    作者:V.E. Platonov、A.M. Maksimov、P.I. Maslovsky
    DOI:10.1016/0022-1139(95)03294-n
    日期:1995.11
    Perfluoro-2,3-dihydrobenzo[b] thiophene (I), along with some quantities of perfluoroindane, has been obtained by copyrolysis of a number of 4-substituted tetrafluorothiophenols with tetrafluoroethylene in the presence of iodine. The interaction of sulphide I with some nucleophilic and oxidizing agents has been studied. The 5-and 6-substituted derivatives of polyfluoro-2,3-dihydrobenzothiophene have
    全氟-2,3-二氢苯并[ b ]噻吩(I)和一些全氟茚满,是通过在碘存在下,将许多4-取代的四氟噻吩酚与四氟乙烯进行共水解而获得的。已经研究了硫化物I与某些亲核试剂和氧化剂的相互作用。已经合成了多氟-2,3-二氢苯并噻吩的5-和6-取代的衍生物。
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