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5-bromo-6-fluorobenzo[b]thiophene | 1404119-54-5

中文名称
——
中文别名
——
英文名称
5-bromo-6-fluorobenzo[b]thiophene
英文别名
5-bromo-6-fluoro-1-benzothiophene
5-bromo-6-fluorobenzo[b]thiophene化学式
CAS
1404119-54-5
化学式
C8H4BrFS
mdl
——
分子量
231.088
InChiKey
AASRSBQIWRXUBV-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):
    3.7
  • 重原子数:
    11
  • 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:
    28.2
  • 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

  • 作为反应物:
    描述:
    5-bromo-6-fluorobenzo[b]thiophene 在 sodium tetrahydroborate 、 间氯过氧苯甲酸 作用下, 以 四氢呋喃1,2-二氯乙烷 为溶剂, 反应 3.0h, 生成 5-bromo-6-fluoro-2,3-dihydrobenzo[b]thiophene 1,1-dioxide
    参考文献:
    名称:
    ANILINO-PYRAZOLE DERIVATIVES, COMPOSITIONS AND METHODS THEREOF
    摘要:
    The invention provides novel anilino-pyrazole derivatives as a cyclin-dependent kinase 2 (CDK2) inhibitors. The invention also provides pharmaceutical compositions comprising the compounds and methods thereof for treating various conditions, diseases and disorders associated with or related to CDK2 activities, or associated with abnormal cell growth, such as tumor growth and cancer.
    公开号:
    WO2023244710A1
  • 作为产物:
    描述:
    4-溴-3-氟苯硫醇磷酸potassium carbonate 作用下, 以 甲苯乙腈 为溶剂, 反应 15.0h, 生成 5-bromo-6-fluorobenzo[b]thiophene
    参考文献:
    名称:
    ANILINO-PYRAZOLE DERIVATIVES, COMPOSITIONS AND METHODS THEREOF
    摘要:
    The invention provides novel anilino-pyrazole derivatives as a cyclin-dependent kinase 2 (CDK2) inhibitors. The invention also provides pharmaceutical compositions comprising the compounds and methods thereof for treating various conditions, diseases and disorders associated with or related to CDK2 activities, or associated with abnormal cell growth, such as tumor growth and cancer.
    公开号:
    WO2023244710A1
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文献信息

  • [EN] 17a-HYDROXYLASE/C17,20-LYASE INHIBITORS<br/>[FR] INHIBITEURS DE 17?-HYDROXYLASE/C17,20-LYASE
    申请人:NOVARTIS AG
    公开号:WO2012149413A1
    公开(公告)日:2012-11-01
    The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5 and R6 are as defined herein. The compounds of the present invention have been found to be useful as 17α-hydroxylase/C17,20-lyase inhibitors.
    本发明提供了Formula (I)的化合物,或其药用可接受的盐,其中R1、R2、R3、R4、R5和R6如本文所定义。本发明的化合物被发现可用作17α-羟化酶/C17,20-裂解酶抑制剂
  • 4-AMINO-6-(HETEROCYCLIC)PICOLINATES AND 6-AMINO-2-(HETEROCYCLIC)PYRIMIDINE-4-CARBOXYLATES AND THEIR USE AS HERBICIDES
    申请人:Dow AgroSciences, LLC
    公开号:US20150126372A1
    公开(公告)日:2015-05-07
    4-Amino-6-(heterocyclic)picolinic acids and their derivatives; 6-amino-2-(heterocyclic)pyrimidine-4-carboxylates and their derivatives; and methods of using the same as herbicides.
    4-基-6-(杂环)吡啶甲酸及其衍生物;6-基-2-(杂环)嘧啶-4-羧酸酯及其衍生物;以及将其作为除草剂的方法。
  • 17a-HYDROXYLASE/C17,20-LYASE INHIBITORS
    申请人:Bock Mark Gary
    公开号:US20140228386A1
    公开(公告)日:2014-08-14
    The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are as defined herein. The compounds of the present invention have been found to be useful as 17α-hydroxylase/C 17,20 -lyase inhibitors.
    本发明提供了式(I)的化合物或其药学上可接受的盐,其中R1、R2、R3、R4、R5和R6如本文所定义。本发明的化合物已被发现可用作17α-羟化酶/C17,20-裂解酶抑制剂
  • 4-amino-6-(heterocyclic)picolinates and 6-amino-2-(heterocyclic)pyrimidine-4-carboxylates and their use as herbicides
    申请人:Dow AgroSciences, LLC
    公开号:US09278985B2
    公开(公告)日:2016-03-08
    4-Amino-6-(heterocyclic)picolinic acids and their derivatives; 6-amino-2-(heterocyclic)pyrimidine-4-carboxylates and their derivatives; and methods of using the same as herbicides.
    4-基-6-(杂环)吡啶甲酸及其衍生物;6-基-2-(杂环)嘧啶-4-羧酸盐及其衍生物;以及将其用作除草剂的方法。
  • 17α-hydroxylase/C17,20-lyase inhibitors
    申请人:Bock Mark Gary
    公开号:US09029399B2
    公开(公告)日:2015-05-12
    The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5 and R6 are as defined herein. The compounds of the present invention have been found to be useful as 17α-hydroxylase/C17,20-lyase inhibitors.
    本发明提供了式(I)的化合物或其药学上可接受的盐,其中R1、R2、R3、R4、R5和R6如本文所定义。本发明的化合物已被发现可用作17α-羟化酶/C17,20-裂解酶抑制剂
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