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3-溴-5-氯喹啉 | 1416440-62-4

中文名称
3-溴-5-氯喹啉
中文别名
——
英文名称
3-bromo-5-chloroquinoline
英文别名
3-Bromo-5-chloroquinoline
3-溴-5-氯喹啉化学式
CAS
1416440-62-4
化学式
C9H5BrClN
mdl
——
分子量
242.502
InChiKey
DNPKBKRTVUSVRU-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:
    311.8±22.0 °C(Predicted)
  • 密度:
    1.673±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2933499090

SDS

SDS:b7a8ca28a6ee50ad205b05dd1072b4fb
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反应信息

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文献信息

  • [EN] 1, 4-SUBSTITUTED PIPERIDINE DERIVATIVES<br/>[FR] DÉRIVÉS DE PIPÉRIDINE 1,4-SUBSTITUÉS
    申请人:CEPHALON INC
    公开号:WO2016205633A1
    公开(公告)日:2016-12-22
    Described herein are 1,4-substituted piperidine compounds according to Formula (I) that have demonstrated activity as fatty acid synthase inhibitors. Also described herein are pharmaceutical compositions containing the described 1,4-substituted piperidine compounds, and methods of treating diseases mediated by fatty acid synthase, by administering one or more of the compounds or pharmaceutical formulations described herein. Also described herein are methods of synthesizing the compounds described, including the described 1,4-substituted piperidine compounds and synthetic intermediates useful in those syntheses.
    本文描述了按照式(I)的1,4-取代哌啶化合物,这些化合物已经表现出作为脂肪酸合成酶抑制剂的活性。本文还描述了含有所述1,4-取代哌啶化合物的药物组合物,以及通过给予所述化合物或药物配方中的一个或多个来治疗由脂肪酸合成酶介导的疾病的方法。本文还描述了合成所述化合物的方法,包括所述的1,4-取代哌啶化合物和在这些合成中有用的合成中间体。
  • 1,4-substituted piperidine derivatives
    申请人:89BIO LTD
    公开号:US10221135B2
    公开(公告)日:2019-03-05
    Described herein are 1,4-substituted piperidine compounds according to Formula I that have demonstrated activity as fatty acid synthase inhibitors. Also described herein are pharmaceutical compositions containing the described 1,4-substituted piperidine compounds, and methods of treating diseases mediated by fatty acid synthase, by administering one or more of the compounds or pharmaceutical formulations described herein. Also described herein are methods of synthesizing the compounds described, including the described 1,4-substituted piperidine compounds and synthetic intermediates useful in those syntheses.
    本文描述了根据式 I 的 1,4-取代的哌啶化合物,这些化合物已被证明具有脂肪酸合酶抑制剂的活性。本文还描述了含有所述 1,4-取代哌啶化合物的药物组合物,以及通过施用一种或多种本文所述化合物或药物制剂治疗由脂肪酸合成酶介导的疾病的方法。本文还描述了合成所述化合物的方法,包括所述 1,4-取代的哌啶化合物和用于这些合成的合成中间体。
  • 1, 4-SUBSTITUTED PIPERIDINE DERIVATIVES
    申请人:89Bio Ltd.
    公开号:EP3310441B1
    公开(公告)日:2020-07-29
  • 1,4-SUBSTITUTED PIPERIDINE DERIVATIVES
    申请人:Cephalon, Inc.
    公开号:US20160368874A1
    公开(公告)日:2016-12-22
    Described herein are 1,4-substituted piperidine compounds according to Formula I that have demonstrated activity as fatty acid synthase inhibitors. Also described herein are pharmaceutical compositions containing the described 1,4-substituted piperidine compounds, and methods of treating diseases mediated by fatty acid synthase, by administering one or more of the compounds or pharmaceutical formulations described herein. Also described herein are methods of synthesizing the compounds described, including the described 1,4-substituted piperidine compounds and synthetic intermediates useful in those syntheses.
  • 1,4-Substituted Piperidine Derivatives
    申请人:89BIO LTD
    公开号:US20210230116A1
    公开(公告)日:2021-07-29
    Described herein are 1,4-substituted piperidine compounds according to Formula I that have demonstrated activity as fatty acid synthase inhibitors. Also described herein are pharmaceutical compositions containing the described 1,4-substituted piperidine compounds, and methods of treating diseases mediated by fatty acid synthase, by administering one or more of the compounds or pharmaceutical formulations described herein. Also described herein are methods of synthesizing the compounds described, including the described 1,4-substituted piperidine compounds and synthetic intermediates useful in those syntheses.
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