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benzyl(2,3,5,6-tetrafluorophenyl)sulfane | 1376608-47-7

中文名称
——
中文别名
——
英文名称
benzyl(2,3,5,6-tetrafluorophenyl)sulfane
英文别名
3-Benzylsulfanyl-1,2,4,5-tetrafluorobenzene;3-benzylsulfanyl-1,2,4,5-tetrafluorobenzene
benzyl(2,3,5,6-tetrafluorophenyl)sulfane化学式
CAS
1376608-47-7
化学式
C13H8F4S
mdl
——
分子量
272.266
InChiKey
CKCJNDIYEBXIEL-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):
    4.3
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    25.3
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    benzyl(2,3,5,6-tetrafluorophenyl)sulfane三氯异氰尿酸溶剂黄146 作用下, 以 乙腈 为溶剂, 反应 2.0h, 以80%的产率得到2,3,5,6-tetrafluorobenzenesulfonyl chloride
    参考文献:
    名称:
    [EN] 2-ARYLSULFONAMIDO-N-ARYLACETAMIDE DERIVATIZED STAT3 INHIBITORS
    [FR] INHIBITEURS DE STAT3 DÉRIVÉS DE 2-ARYLSULFONAMIDO-N-ARYLACÉTAMIDE
    摘要:
    本公开提供了含有2-芳基磺酰胺基-N-芳基乙酰胺衍生的Stat3抑制剂及其某些药用盐的制药组合物,以及它们的使用方法。
    公开号:
    WO2018136935A1
  • 作为产物:
    描述:
    硫代乙酸苄酯五氟苯potassium carbonateL-脯氨酸 、 copper(I) bromide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 以58%的产率得到benzyl(2,3,5,6-tetrafluorophenyl)sulfane
    参考文献:
    名称:
    Regioselective C–S bond formation accomplished by copper-catalyzed regioselective C–F substitution of perfluoroarenes with aryl thioacetates or benzyl thioacetate
    摘要:
    Practical and straightforward method for regioselective C-S bond formation accomplished by copper-catalyzed regioselective C-F substitution of electron-deficient perfluoroarenes with aryl thioacetates or benzyl thioacetate has been developed. Because of its high reaction efficiency, good chemoselectivity and regioselectivity, and excellent functional-group compatibility, this protocol provides a useful and operationally simple access to polyfluoroaryl thioethers used for drugs and material chemistry. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.03.091
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文献信息

  • Synthesis of polyfluorinated aromatic ethers and thioethers by synergistic cleavage of C-B bond and C-F bond of B(C6F5)3
    作者:Cui-Cui Ma、Xing-Xing Zhu、Li Liu、Jian-Jun Dai、Jun Xu、Hua-Jian Xu
    DOI:10.1016/j.tetlet.2021.153387
    日期:2021.10
    A concise and efficient method for the synthesis of polyfluorinated aromatic ethers and thioethers by synergistic cleavage of C-B bond and C-F bond of B(C6F5)3 is reported. The reaction could proceed smoothly with excellent functional-group compatibility. In addition, the transformation represents the first general application of B(C6F5)3 as reaction partners in cross-coupling reaction.
    报道了一种通过协同裂解 B(C 6 F 5 ) 3的 CB 键和 CF 键合成多氟芳族醚和硫醚的简洁有效的方法。反应可以顺利进行,具有良好的官能团相容性。此外,该转变代表了 B(C 6 F 5 ) 3作为交叉偶联反应中的反应伙伴的首次普遍应用。
  • [EN] 2-ARYLSULFONAMIDO-N-ARYLACETAMIDE DERIVATIZED STAT3 INHIBITORS<br/>[FR] INHIBITEURS DE STAT3 DÉRIVÉS DE 2-ARYLSULFONAMIDO-N-ARYLACÉTAMIDE
    申请人:UNIV HAWAII
    公开号:WO2018136935A1
    公开(公告)日:2018-07-26
    The present disclosure provides pharmaceutical compositions comprising 2-arylsulfonamido-N-arylacetamide derivatized Stat3 inhibitors and certain pharmaceutically acceptable salts thereof, and methods of their use.
    本公开提供了含有2-芳基磺酰胺基-N-芳基乙酰胺衍生的Stat3抑制剂及其某些药用盐的制药组合物,以及它们的使用方法。
  • Regioselective C–S bond formation accomplished by copper-catalyzed regioselective C–F substitution of perfluoroarenes with aryl thioacetates or benzyl thioacetate
    作者:Qizhong Zhou、Bin Zhang、Tieqi Du、Haining Gu、Huajiang Jiang、Rener Chen
    DOI:10.1016/j.tet.2012.03.091
    日期:2012.6
    Practical and straightforward method for regioselective C-S bond formation accomplished by copper-catalyzed regioselective C-F substitution of electron-deficient perfluoroarenes with aryl thioacetates or benzyl thioacetate has been developed. Because of its high reaction efficiency, good chemoselectivity and regioselectivity, and excellent functional-group compatibility, this protocol provides a useful and operationally simple access to polyfluoroaryl thioethers used for drugs and material chemistry. (C) 2012 Elsevier Ltd. All rights reserved.
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