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β-chloroethyl 2-thienyl sulfide | 55697-87-5

中文名称
——
中文别名
——
英文名称
β-chloroethyl 2-thienyl sulfide
英文别名
(2-Chlorethyl)-(2-thienyl)-sulfid;2-(β-Chlorethylmercapto)-thiophen;1-chloro-2-(thien-2-ylthio)ethane;2-(2-chloroethylthio)thiophene;2-(2-chloro-ethylsulfanyl)-thiophene;1-chloro-2-(2-thienylthio)ethane;Thiophene, 2-[(2-chloroethyl)thio]-;2-(2-chloroethylsulfanyl)thiophene
β-chloroethyl 2-thienyl sulfide化学式
CAS
55697-87-5
化学式
C6H7ClS2
mdl
——
分子量
178.707
InChiKey
QGMBRBQQSIWZPS-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:
    118-120 °C(Press: 2.5 Torr)
  • 密度:
    1.2811 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    53.5
  • 氢给体数:
    0
  • 氢受体数:
    2

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

点击查看最新优质反应信息

文献信息

  • Use of azacyclic or azabicyclic thiadiazole compounds for treating anxiety
    申请人:ELI LILLY AND COMPANY
    公开号:EP0774256A1
    公开(公告)日:1997-05-21
    The present invention provides a method for treating anxiety in humans using azacyclic or azabicyclic thiadiazole compounds.
    本发明提供了一种治疗人类焦虑症的方法,使用氮杂环或氮杂双环噻二唑化合物。
  • Heterocyclic compounds and their preparation and use
    申请人:ELI LILLY AND COMPANY
    公开号:EP0709381A1
    公开(公告)日:1996-05-01
    The present invention relates to therapeutically active azacyclic or azabicyclic compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds. The novel compounds are useful in treating diseases in the central nervous system caused by malfunctioning of the muscarinic cholinergic system, and are of formula I or the quarternized form thereof
    本发明涉及具有治疗活性的氮杂环或氮杂双环化合物、制备方法以及包含这些化合物的药物组合物。这些新型化合物可用于治疗因毒蕈碱胆碱能系统功能失调而引起的中枢神经系统疾病,它们是式 I 或其醌化形式
  • ——
    作者:O. V. Alekminskaya、N. V. Russavskaya、N. A. Korchevin、E. N. Deryagina
    DOI:10.1023/a:1015397313038
    日期:——
    A convenient preparative synthesis of bis(organylthio)alkanes was developed. It is based on alkylation with dihaloalkanes of solutions of diorganyl disulfides in the basic reductive system hydrazine hydrate-alkali. The generation of organylthiolate anions from disulfides and the subsequent reaction of the anions with dihaloalkanes are performed in one reaction vessel without isolation of intermediate alkali metal thiolates. At the same time, the reactions of diphenyl or dithienyl disulfides with dihaloalkanes result in substitution with the thiolate anions of only one halogen atom to give the corresponding unsymmetrical sulfides. In certain cases in the presence of excess alkali the latter sulfides are dehalogenated to form alkyl vinyl sulfides.
  • ——
    作者:N. V. Russavskaya、N. A. Korchevin、O. V. Alekminskaya、E. N. Sukhomazova、E. P. Levanova、E. N. Deryagina
    DOI:10.1023/a:1022540002086
    日期:——
    Reaction of thiols with dihaloalkanes in the system hydrazine hydrate-base leads to alkyl(chloroalkyl) sulfides with different positions of the chlorine atom with respect to sulfur. The developed one-step procedure for the synthesis of such unsymmetrical sulfides is most suitable for arenethiols and alkanethiols having a long polymethylene chain. The reaction mechanism is discussed.
  • ETIENNE A.; BAILLS G.; LONCHAMBON G.; DESMAZIERES B., C. R. ACAD. SCI., 1979, C 288, NO 19, 493-498
    作者:ETIENNE A.、 BAILLS G.、 LONCHAMBON G.、 DESMAZIERES B.
    DOI:——
    日期:——
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