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5-(2,2,2-trifluoroethoxy)thiophene-2-carbaldehyde

中文名称
——
中文别名
——
英文名称
5-(2,2,2-trifluoroethoxy)thiophene-2-carbaldehyde
英文别名
——
5-(2,2,2-trifluoroethoxy)thiophene-2-carbaldehyde化学式
CAS
——
化学式
C7H5F3O2S
mdl
——
分子量
210.177
InChiKey
KMZOASLHNMYBAF-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):
    2.5
  • 重原子数:
    13.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    26.3
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为产物:
    描述:
    5-溴噻吩-2-甲醛2,2,2-三氟乙醇potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 20.0h, 以66%的产率得到5-(2,2,2-trifluoroethoxy)thiophene-2-carbaldehyde
    参考文献:
    名称:
    [EN] ANTIBACTERIAL AGENTS: ARYL MYXOPYRONIN DERIVATIVES
    [FR] AGENTS ANTIBACTÉRIENS : DÉRIVÉS ARYL MYXOPYRONINES
    摘要:
    该发明提供了以下公式的化合物:[公式 Ia、Ib 和 Ic] 及其盐,其中变量如规范中所述,以及包含公式 Ia-Ic 化合物的组合物、制备这种化合物的方法以及使用这种化合物的方法,例如作为细菌RNA聚合酶的抑制剂和抗菌剂。
    公开号:
    WO2013192352A1
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文献信息

  • ANTIBACTERIAL AGENTS: ARYL MYXOPYRONIN DERIVATIVES
    申请人:RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY
    公开号:US20150197512A1
    公开(公告)日:2015-07-16
    The invention provides compounds of formula la, lb and Ic: [Formula Ia, Ib, and Ic] and salts thereof, wherein variables are as described in the specification, as well as compositions comprising a compound of formula Ia-Ic, methods of making such compounds, and methods of using such compounds, e.g., as inhibitors of bacterial RNA polymerase and as antibacterial agents.
    本发明提供了公式la、lb和Ic的化合物:[公式Ia、Ib和Ic]及其盐,其中变量如规范所述,以及包含化合物Ia-Ic的组合物,制备这种化合物的方法和使用这种化合物的方法,例如作为细菌RNA聚合酶的抑制剂和抗菌剂。
  • Antibacterial agents: aryl myxopyronin derivatives
    申请人:RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY
    公开号:US09315495B2
    公开(公告)日:2016-04-19
    The invention provides compounds of formula la, lb and Ic: [Formula Ia, Ib, and Ic] and salts thereof, wherein variables are as described in the specification, as well as compositions comprising a compound of formula Ia-Ic, methods of making such compounds, and methods of using such compounds, e.g., as inhibitors of bacterial RNA polymerase and as antibacterial agents.
    本发明提供公式Ia、Ib和Ic的化合物及其盐,其中变量如说明书所述,以及包含化合物Ia-Ic的组合物、制备这样的化合物的方法和使用这样的化合物的方法,例如作为细菌RNA聚合酶的抑制剂和抗菌剂。
  • VOLTAGE-DEPENDENT T-TYPE CALCIUM CHANNEL INHIBITOR
    申请人:Nippon Chemiphar Co., Ltd.
    公开号:EP3404021A1
    公开(公告)日:2018-11-21
    A compound represented by the following General Formula (I), a tautomer or a stereoisomer of the compound, a pharmaceutically acceptable salt thereof, or a solvate thereof, is used as a voltage-dependent T-type calcium channel blocker: wherein A represents a fused ring which may have a substituent, the fused ring being composed of a 5-membered heteroaryl group or a 5-membered or 6-membered heterocyclic ring and a benzene ring or the like, the 5-membered heteroaryl group having one to three identical or different heteroatoms as a ring-constituting element(s) having at least one substituent such as an alkoxy group having 1 to 8 carbon atoms and substituted with 1 to 5 halogen atoms; R represents a hydrogen atom or the like; B represents CR5(Q1) or NQ2, herein Q1 represents a benzimidazole group which may have a substituent; Q2 represents an alkyl group having 1 to 8 carbon atoms which may have a substituent, a heteroaryl group which may have a substituent, or the like; R0, R1, R2, R3, R4, and R5 each represent a hydrogen atom or the like; and n and m each represent 0, 1, or 2, provide that n and m are not 0 and 2 at the same time.
    由以下通式(I)代表的化合物、该化合物的同系物或立体异构体、其药学上可接受的盐或其溶液可用作电压依赖性 T 型钙通道阻滞剂: 其中 A 代表可具有取代基的融合环,该融合环由 5 元杂芳基或 5 元或 6 元杂环和苯环或类似物组成,5 元杂芳基具有 1 至 3 个相同或不同的杂原子作为成环元素,具有至少一个取代基,例如具有 1 至 8 个碳原子并被 1 至 5 个卤素原子取代的烷氧基;R 代表氢原子或类似物;B 代表 CR5(Q1) 或 NQ2,其中 Q1 代表可能具有取代基的苯并咪唑基;Q2 代表可能具有取代基的具有 1 至 8 个碳原子的烷基、可能具有取代基的杂芳基或类似物;R0、R1、R2、R3、R4 和 R5 各代表氢原子或类似物;n 和 m 各代表 0、1 或 2,但 n 和 m 不能同时为 0 和 2。
  • VOLTAGE-DEPENDENT T-TYPE CALCIUM CHANNEL BLOCKER
    申请人:Nippon Chemiphar Co., Ltd.
    公开号:US20190077767A1
    公开(公告)日:2019-03-14
    A compound represented by the following General Formula (I), a tautomer or a stereoisomer of the compound, a pharmaceutically acceptable salt thereof, or a solvate thereof, is used as a voltage-dependent T-type calcium channel blocker: wherein A represents a fused ring which may have a substituent, the fused ring being composed of a 5-membered heteroaryl group or a 5-membered or 6-membered heterocyclic ring and a benzene ring or the like, the 5-membered heteroaryl group having one to three identical or different heteroatoms as a ring-constituting element(s) having at least one substituent such as an alkoxy group having 1 to 8 carbon atoms and substituted with 1 to 5 halogen atoms; R represents a hydrogen atom or the like; B represents CR5(Q1) or NQ2, herein Q1 represents a benzimidazole group which may have a substituent; Q2 represents an alkyl group having 1 to 8 carbon atoms which may have a substituent, a heteroaryl group which may have a substituent, or the like; R0, R1, R2, R3, R4, and R5 each represent a hydrogen atom or the like; and n and m each represent 0, 1, or 2, provide that n and m are not 0 and 2 at the same time.
  • US9315495B2
    申请人:——
    公开号:US9315495B2
    公开(公告)日:2016-04-19
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