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1-甲基-5-(三氟甲基)-1H-吲哚-2-羧酸 | 1257092-36-6

中文名称
1-甲基-5-(三氟甲基)-1H-吲哚-2-羧酸
中文别名
——
英文名称
1-methyl-5-(trifluoromethyl)-1H-indole-2-carboxylic acid
英文别名
1-methyl-5-(trifluoromethyl)indole-2-carboxylic acid
1-甲基-5-(三氟甲基)-1H-吲哚-2-羧酸化学式
CAS
1257092-36-6
化学式
C11H8F3NO2
mdl
MFCD18839099
分子量
243.185
InChiKey
BJHNBAXVLXMLIM-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):
    2.9
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.181
  • 拓扑面积:
    42.2
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

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文献信息

  • CONDENSED HETEROCYCLIC COMPOUNDS AND PESTICIDES
    申请人:Nissan Chemical Industries, Ltd.
    公开号:US20180022760A1
    公开(公告)日:2018-01-25
    To provide novel pesticides, especially insecticides or acaricides. A condensed heterocyclic compound represented by the formula (1) or its salt or an N-oxide thereof: wherein D substituted with —S(O) n R 1 is a ring represented by any one of D1, D2 and D3, Q is a ring represented by any one of Q1, Q2, Q3 and Q4, R 1 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, (C 1 -C 6 ) alkyl optionally substituted with R 1a , C 2 -C 6 alkenyl, C 2 -C 6 haloalkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkynyl, C 3 -C 6 cycloalkyl, C 3 -C 6 halocycloalkyl, C 3 -C 6 cycloalkyl (C 1 -C 6 ) alkyl, C 3 -C 6 halocycloalkyl (C 1 -C 6 ) alkyl or hydroxy (C 1 -C 6 ) alkyl, R 1a is C 1 -C 8 alkoxycarbonyl, and n is an integer of 0, 1 or 2.
    提供新型杀虫剂,特别是杀虫剂杀螨剂。由式(1)表示的缩合杂环化合物或其盐或其N-氧化物: 其中D被—S(O)nR1取代,是由D1、D2和D3中的任何一个表示的环,Q是由Q1、Q2、Q3和Q4中的任何一个表示的环,R1是C1-C6烷基,C1-C6卤代烷基,(C1-C6)烷基,可选地取代R1a,C2-C6烯基,C2-C6卤代烯基,C2-C6炔基,C2-C6卤代炔基,C3-C6环烷基,C3-C6卤代环烷基,C3-C6环烷基(C1-C6)烷基,C3-C6卤代环烷基(C1-C6)烷基或羟基(C1-C6)烷基,R1a是C1-C8烷氧羰基,n是0、1或2的整数。
  • ARYL SUBSTITUTED CARBOXAMIDE DERIVATIVES AS CALCIUM OR SODIUM CHANNEL BLOCKERS
    申请人:Inoue Tadashi
    公开号:US20120101105A1
    公开(公告)日:2012-04-26
    The present invention relates to aryl substituted carboxamide derivatives of formula (I) or a pharmaceutically acceptable salt thereof, which have blocking activities of T-type calcium channels or voltage gated sodium channels as the tetrodotoxin-sensitive (TTX-S) blockers such as Na v1.3 and Na v1.7 , and which are useful in the treatment or prevention of disorders and diseases in which T-type calcium channels or voltage gated sodium channels are involved. The invention also relates to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which T-type calcium channels or voltage gated sodium channels are involved.
    本发明涉及公式(I)或其药学上可接受的盐的芳基取代羧酰胺衍生物,其具有T型通道或电压门控通道的阻滞活性,如Nav1.3和Nav1.7等Tetrodotoxin敏感(TTX-S)阻滞剂,并且在涉及T型通道或电压门控通道的疾病或疾病的治疗或预防中有用。本发明还涉及包含这些化合物的制药组合物以及在涉及T型通道或电压门控通道的疾病或疾病的预防或治疗中使用这些化合物和组合物的用途。
  • Condensed heterocyclic compounds and pesticides
    申请人:NISSAN CHEMICAL CORPORATION
    公开号:US10464950B2
    公开(公告)日:2019-11-05
    To provide novel pesticides, especially insecticides or acaricides. A condensed heterocyclic compound represented by the formula (1) or its salt or an N-oxide thereof: wherein D substituted with —S(O)nR1 is a ring represented by any one of D1, D2 and D3, Q is a ring represented by any one of Q1, Q2, Q3 and Q4, R1 is C1-C6 alkyl, C1-C6 haloalkyl, (C1-C6) alkyl optionally substituted with R1a, C2-C6 alkenyl, C2-C6 haloalkenyl, C2-C6 alkynyl, C2-C6 haloalkynyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 cycloalkyl (C1-C6) alkyl, C3-C6 halocycloalkyl (C1-C6) alkyl or hydroxy (C1-C6) alkyl, R1a is C1-C8 alkoxycarbonyl, and n is an integer of 0, 1 or 2.
    提供新型杀虫剂,特别是杀虫剂杀螨剂。 一种由式(1)代表的缩合杂环化合物或其盐或其 N-氧化物: C2-C6 卤代烯基、C2-C6 烷基、C2-C6 卤代炔基、C3-C6 环烷基、C3-C6 卤代环烷基、C3-C6 环(C1-C6)烷基、C3-C6 卤代环(C1-C6)烷基或羟基(C1-C6)烷基,R1a 是 C1-C8 烷氧羰基,n 是 0、1 或 2 的整数。
  • CONDENSED HETEROCYCLIC COMPOUND AND NOXIOUS ORGANISM CONTROL AGENT
    申请人:Nissan Chemical Corporation
    公开号:EP3257853B1
    公开(公告)日:2021-11-10
  • THERAPEUTIC INHIBITORY COMPOUNDS
    申请人:LifeSci Pharmaceuticals, Inc.
    公开号:US20170029406A1
    公开(公告)日:2017-02-02
    Provided herein are heterocyclic derivative compounds and pharmaceutical compositions comprising said compounds that are useful for inhibiting plasma kallikrein. Furthermore, the subject compounds and compositions are useful for the treatment of diseases wherein the inhibition of plasma kallikrein inhibition has been implicated, such as angioedema and the like.
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