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4-bromo-5-(1-fluoroethenyl)-3-methylthiophene-2-carboxaldehyde

中文名称
——
中文别名
——
英文名称
4-bromo-5-(1-fluoroethenyl)-3-methylthiophene-2-carboxaldehyde
英文别名
4-bromo-5-(1'-fluorovinyl)-3-methyl 2-carboxaldehydethiophene;4-bromo-5-(1-fluorovinyl)-3-methylthiophene-2-carbaldehyde;4-Bromo-5-(1-fluoroethenyl)-3-methylthiophene-2-carbaldehyde
4-bromo-5-(1-fluoroethenyl)-3-methylthiophene-2-carboxaldehyde化学式
CAS
——
化学式
C8H6BrFOS
mdl
——
分子量
249.103
InChiKey
IMYCIOWDONUZTO-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):
    3.2
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    45.3
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • Substituted thiophenes with antibacterial activity
    申请人:Berge John
    公开号:US20050009833A1
    公开(公告)日:2005-01-13
    Novel substituted thiophenes that are inhibitors of bacterial methionyl t-RNA synthetase (MRS) are disclosed. Also disclosed are method for their preparation and their use in therapy as anti-bacterial agents.
    本发明揭示了一种替代噻吩的小说抑制细菌甲酰-tRNA合成酶(MRS)的化合物。同时,本发明还揭示了它们的制备方法以及它们作为抗菌药物在治疗中的应用。
  • 2-NH-heteroarylimidazoles with antibacterial activity
    申请人:Berge John
    公开号:US20060014748A1
    公开(公告)日:2006-01-19
    Compounds of formula (I): are inhibitors of bacterial methionyl tRNA synthetase and are of use in treating bacterial infections.
    公式(I)的化合物是细菌甲酸tRNA合成酶抑制剂,可用于治疗细菌感染。
  • 2-NH-HETEROARYLIMIDAZOLES WITH ANTIBACTERIAL ACTIVITY
    申请人:Berge John
    公开号:US20070213362A1
    公开(公告)日:2007-09-13
    A method of inhibiting MetRS activity comprises administering to a patient in need thereof a MetRS inhibiting effective amount of a compound of the formula (I). A method of treating a resistant or multiply-resistant E. faecalis infection, a resistant or multiply-resistant S. aureus infection, and/or a resistant or multiply-resistant S. epidermidis infection comprises administering to a patient in need thereof an antibacterially effective amount of a compound of the formula (I).
    一种抑制MetRS活性的方法包括向需要治疗的患者投予化合物(I)的抑制剂有效量。一种治疗耐药或多重耐药E. faecalis感染,耐药或多重耐药S. aureus感染和/或耐药或多重耐药S. epidermidisinfection的方法包括向需要治疗的患者投予化合物(I)的抗菌有效量。
  • Transition Metal Catalyzed Cross-Coupling Of 1-Halo-1-Haloalkene Compounds
    申请人:Guiles Joseph W.
    公开号:US20080194842A1
    公开(公告)日:2008-08-14
    Methods for introducing a 1-halo-1-haloalkene compound onto an aromatic or heteroaromatic ring are provided, including processes for the production of certain 1-halovinyl aryl or heteroaryl derivatives in which the 1-halovinyl group is either 1-fluoro or 1-chlorovinyl and the aromatic species phenyl or thiophene, the processes including coupling an arylmagnesium species with a dihalo olefin in the presence of a nickel or iron catalyst.
    提供了将1-卤代-1-卤代化合物引入芳香或杂芳环上的方法,包括生产某些1-卤代乙烯基芳基或杂芳基衍生物的过程,其中1-卤代乙烯基团为1-乙烯基或1-乙烯基,芳基物种为基或噻吩,该过程包括在催化剂存在下将芳基物种与二卤代烃偶联的步骤。
  • Transition metal catalyzed cross-coupling of 1-halo-1-haloalkene compounds
    申请人:Guiles Joseph W.
    公开号:US20090054667A1
    公开(公告)日:2009-02-26
    Methods for introducing a 1-halo-1-haloalkene compound onto an aromatic or heteroaromatic ring are provided, including processes for the production of certain 1-halovinyl aryl or heteroaryl derivatives in which the 1-halovinyl group is either 1-fluoro or 1-chlorovinyl and the aromatic species phenyl or thiophene, the processes including coupling an arylmagnesium species with a dihalo olefin in the presence of a nickel or iron catalyst.
    提供了一种将1-卤代化合物引入芳香环或杂环芳烃的方法,包括生产某些1-卤代乙烯基芳基或杂芳基衍生物的过程,其中1-卤代乙烯基团是1-乙烯基或1-乙烯基,芳香物种是噻吩,该过程包括在催化剂存在下将芳基物种与二卤代烃偶联。
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