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3-(3-trifluoromethylphenyl)-piperidine hydrochloride | 64321-43-3

中文名称
——
中文别名
——
英文名称
3-(3-trifluoromethylphenyl)-piperidine hydrochloride
英文别名
3-(m-trifluoromethylphenyl)-piperidine hydrochloride;hydron;3-[3-(trifluoromethyl)phenyl]piperidine;chloride
3-(3-trifluoromethylphenyl)-piperidine hydrochloride化学式
CAS
64321-43-3
化学式
C12H14F3N*ClH
mdl
MFCD01756638
分子量
265.706
InChiKey
RUABMLQEAISSGG-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):
    3.03
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    12
  • 氢给体数:
    2
  • 氢受体数:
    4

SDS

SDS:671ed0e58725d8126a1dbf856042662d
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反应信息

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文献信息

  • [EN] 2,3-DIHYDROBENZO(1,4) DIOXIN-2-YLMETHYL DERIVATIVES AS ALPHA2C ANTAGONISTS FOR USE IN THE TREATMENT OF PERIPHERIC AND CENTRAL NERVOUS SYSTEM DISEASES<br/>[FR] DÉRIVÉS DE 2,3-DIHYDROBENZO[1,4] DIOXIN-2-YLMÉTHYLE UTILISÉS EN TANT QU'ANTAGONISTES DES ALPHA2C POUR TRAITER DES MALADIES DES SYSTÈMES NERVEUX PÉRIPHÉRIQUE ET CENTRAL
    申请人:ORION CORP
    公开号:WO2009013390A1
    公开(公告)日:2009-01-29
    Compounds of formula (I), wherein X, Z, R1-R4, and m are as defined in the claims, exhibit alpha2C antagonistic activity and are thus useful for the treatment of diseases and conditions of the peripheric system and the central nervous system (CNS).
    式(I)的化合物,其中X、Z、R1-R4和m如权利要求中所定义,具有α2C拮抗活性,因此可用于治疗外周系统和中枢神经系统(CNS)的疾病和症状。
  • [EN] [3-HETEROARYL-2-TRIFLUOROMETHYL-PROPYL]-PIPERIDIN-1-YLE OR -MORPHOLIN-4-YLE COMPOUNDS AS TRPA1 ANTAGONISTS FOR THE TREATMENT OF RESPIRATORY DISEASES<br/>[FR] COMPOSÉS [3-HÉTÉROARYL-2-TRIFLUOROMÉTHYL-PROPYL]-PIPÉRIDIN-1-YLE OU -MORPHOLIN-4-YLE EN TANT QU'ANTAGONISTES DE TRPA1 POUR LE TRAITEMENT DE MALADIES RESPIRATOIRES
    申请人:HOFFMANN LA ROCHE
    公开号:WO2014072325A1
    公开(公告)日:2014-05-15
    The invention is concerned with the compounds of formula (I) and pharmaceutically acceptable salts thereof. In addition, the present invention relates to methods of manufacturing and using the compounds of formula (I) as well as pharmaceutical compositions containing such compounds. The compounds of formula (I) are antagonists of the TRPA1 channel and may be useful in treating inflammatory diseases and disorders associated with that channel.
    本发明涉及公式(I)的化合物及其药用可接受的盐。此外,本发明涉及制造和使用公式(I)化合物的方法,以及含有这种化合物的药物组合物。公式(I)化合物是TRPA1通道的拮抗剂,可能对治疗与该通道相关的炎症性疾病和紊乱有用。
  • Method for using m-trifluoromethylphenyl-piperidines
    申请人:Roussel Uclaf
    公开号:US04259337A1
    公开(公告)日:1981-03-31
    Novel m-trifluoromethylphenyl-piperidines of the formula ##STR1## wherein R is selected from the group consisting of hydrogen, branched or straight chain alkyl of 1 to 5 carbon atoms, alkenyl of 3 to 5 carbon atoms, alkynyl of 3 to 5 carbon atoms and phenyl alkyl of 1 to 3 alkyl carbon atoms and their non-toxic, pharmaceutically acceptable acid addition salts having antidepressive, anorexigenic and antiparkinsonian activity and their preparation and novel intermediates formed therein.
    化合物的名称为新型m-三氟甲基苯基哌啶,其化学式为##STR1##其中R选择自氢、1至5个碳原子的支链或直链烷基、3至5个碳原子的烯基、3至5个碳原子的炔基和1至3个烷基碳原子的苯基烷基,以及其无毒、药用可接受的酸盐,具有抗抑郁、厌食和抗帕金森病活性,以及其制备和形成的新型中间体。
  • 2,3-DIHYDROBENZO(1,4) DIOXIN-2-YLMETHYL DERIVATIVES AS ALPHA2C ANTAGONISTS FOR USE IN THE TREATMENT OF PERIPHERIC AND CENTRAL NERVOUS SYSTEME DISEASES
    申请人:Din Belle David
    公开号:US20120035210A9
    公开(公告)日:2012-02-09
    Compounds of formula I wherein X, Z, R 1 -R 4 , and m are as defined in the claims, exhibit alpha2C antagonistic activity, and are thus useful as alpha2C antagonists. Methods for the treatment of diseases and conditions of the peripheric system and the central nervous system are also disclosed.
    式I的化合物,其中X、Z、R1-R4和m如权利要求所定义,表现出α2C拮抗活性,因此可用作α2C拮抗剂。还公开了治疗外周系统和中枢神经系统疾病和病症的方法。
  • 2,3-DIHYDROBENZO(1,4) DIOXIN-2-YLMETHYL DERIVATIVES AS ALPHA2C ANTAGONISTS FOR USE IN THE TREATMENT OF PERIPHERIC AND CENTRAL NERVOUS SYSTEM DISEASES
    申请人:ORION CORPORATION
    公开号:US20130281486A1
    公开(公告)日:2013-10-24
    Compounds of formula I wherein X, Z, R 1 -R 4 , and m are as defined in the claims, exhibit alpha2C antagonistic activity, and are thus useful as alpha2C antagonists. Methods for the treatment of diseases and conditions of the peripheric system and the central nervous system are also disclosed.
    式(I)的化合物,其中X、Z、R1-R4和m如权利要求中所定义,表现出α2C拮抗活性,因此可用作α2C拮抗剂。还公开了治疗外周系统和中枢神经系统疾病和病况的方法。
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