摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-(trifluoromethyl)pyrazine-2-carboxylic acid | 1060812-74-9

中文名称
——
中文别名
——
英文名称
6-(trifluoromethyl)pyrazine-2-carboxylic acid
英文别名
——
6-(trifluoromethyl)pyrazine-2-carboxylic acid化学式
CAS
1060812-74-9
化学式
C6H3F3N2O2
mdl
MFCD13189474
分子量
192.097
InChiKey
XSTQESYINDCIJM-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

物化性质

  • 沸点:
    274.6±40.0 °C(Predicted)
  • 密度:
    1.575±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    63.1
  • 氢给体数:
    1
  • 氢受体数:
    7

安全信息

  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] CYCLOBUTYL SUBSTITUTED PYRROLOPYRIDINE AND PYRROLOPYRIMIDINE DERIVATIVES AS JAK INHIBITORS<br/>[FR] DÉRIVÉS PYRROLOPYRIDINE ET PYRROLOPYRIMIDINE À SUBSTITUTION CYCLOBUTYLE UTILISÉS COMME INHIBITEURS DES JAK
    申请人:INCYTE CORP
    公开号:WO2012068450A1
    公开(公告)日:2012-05-24
    The present invention provides cyclobutyl substituted pyrrolopyrimidines and pyrrolopyridines of Formula I: wherein X, Y, Z, L, A, R5, n and m are defined above, as well as their compositions and methods of use, that modulate the activity of Janus kinases (JAKs) and are useful in the treatment of diseases related to the activity of JAKs including, for example, inflammatory disorders, autoimmune disorders, cancer, and other diseases.
    本发明提供了式I的环丁基取代的吡咯嘧啶吡咯吡啶:其中X、Y、Z、L、A、R5、n和m如上定义,以及它们的组合物和使用方法,用于调节Janus激酶(JAKs)的活性,并且在治疗与JAKs活性相关的疾病中是有用的,例如炎症性疾病、自身免疫疾病、癌症和其他疾病。
  • [EN] IMIDAZOPYRIDAZINES AS MODULATORS OF IL-17<br/>[FR] IMIDAZOPYRIDAZINES EN TANT QUE MODULATEURS DE L'IL-17
    申请人:JANSSEN BIOTECH INC
    公开号:WO2021222404A1
    公开(公告)日:2021-11-04
    The present application discloses compounds having the following formula: (I), or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4 and R5 are defined in the specification, as well as methods of making and using the compounds disclosed herein for treating or ameliorating an IL-17 mediated syndrome, disorder and/or disease.
    本申请公开了具有以下公式(I)的化合物,或其药用可接受的盐,其中R1、R2、R3、R4和R5在说明书中定义,以及制造和使用所公开化合物的方法,用于治疗或改善IL-17介导的综合征、紊乱和/或疾病。
  • PIPERIDIN-4-YL AZETIDINE DERIVATIVES AS JAK1 INHIBITORS
    申请人:Huang Taisheng
    公开号:US20110224190A1
    公开(公告)日:2011-09-15
    The present invention provides piperidin-4-yl azetidine derivatives, as well as their compositions and methods of use, that modulate the activity of Janus kinase 1 (JAK1) and are useful in the treatment of diseases related to the activity of JAK1 including, for example, inflammatory disorders, autoimmune disorders, cancer, and other diseases.
    本发明提供了哌啶-4-基氮杂环丙烷生物,以及它们的组合物和使用方法,这些衍生物调节Janus激酶1(JAK1)的活性,并且在治疗与JAK1活性相关的疾病方面具有用处,例如炎症性疾病、自身免疫性疾病、癌症和其他疾病。
  • NOVEL COMPOUNDS
    申请人:HEIMANN Annekatrin
    公开号:US20130158042A1
    公开(公告)日:2013-06-20
    This invention relates to compounds of formula I their use as positive allosteric modulators of mGlu5 receptor activity, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of neurological and psychiatric disorders associated with glutamate dysfunction such as schizophrenia or cognitive decline such as dementia or cognitive impairment. R 1 , R 2 , R 3 , R 4 , Q have meanings given in the description.
    这项发明涉及公式I的化合物,它们作为mGlu5受体活性的正向变构调节剂的用途,含有这些化合物的药物组合物,以及将其用作治疗和/或预防与谷酸功能障碍相关的神经和精神障碍,如精神分裂症或认知功能下降,如痴呆症或认知障碍的药剂的方法。R1,R2,R3,R4,Q在描述中给出了含义。
  • [EN] PYRAZINE DERIVATIVES<br/>[FR] DÉRIVÉS DE PYRAZINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2014072257A1
    公开(公告)日:2014-05-15
    The present invention relates to compounds of formula (I), wherein R1R2 are hydrogen, lower alkyl, lower alkoxy, lower alkyl substituted by halogen, lower alkoxy substituted by halogen, cycloalkyl, OCH2-cycloalkyl or heterocycloalkyl which is optionally substituted by halogen, with the proviso that one of R1 and R2 is hydrogen, or R1 and R2 form together with the carbon atom to which they are attach a phenyl ring, which may be optionally substituted by lower alkyl; R3/R4 are hydrogen, halogen or cyano; with the proviso that one of R3 and R4 is hydrogen; or to a pharmaceutically suitable acid addition salt thereof, to all racemic mixtures, all their corresponding enantiomers and/or optical isomers, which may be used for the treatment of depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), stress-related disorders, psychotic disorders, schizophrenia, neurological diseases, Parkinson's disease, neurodegenerative disorders, Alzheimer's disease, epilepsy, migraine, hypertension, substance abuse, metabolic disorders, eating disorders, diabetes, diabetic complications, obesity, dyslipidemia, disorders of energy consumption and assimilation, disorders and malfunction of body temperature homeostasis, disorders of sleep and circadian rhythm, and cardiovascular disorders.
    本发明涉及式(I)的化合物,其中R1R2为氢、较低的烷基、较低的烷氧基、受卤素取代的较低烷基、受卤素取代的较低烷氧基、环烷基、OCH2-环烷基或杂环烷基,该杂环烷基可以选择性地受卤素取代,但R1和R2中的一个为氢,或者R1和R2与它们连接的碳原子一起形成苯环,该苯环可以选择性地受较低烷基取代;R3/R4为氢、卤素或基;但R3和R4中的一个为氢;或其药学上适宜的酸盐,所有的外消旋混合物,它们对应的对映体和/或光学异构体,可用于治疗抑郁症、焦虑症、躁郁症、注意缺陷多动障碍(ADHD)、与压力有关的疾病、精神疾病、精神分裂症、神经系统疾病、帕森病、神经退行性疾病、阿尔茨海默病、癫痫、偏头痛、高血压、物质滥用、代谢紊乱、进食障碍、糖尿病、糖尿病并发症、肥胖症、血脂异常、能量消耗和吸收障碍、体温稳态障碍、睡眠和昼夜节律障碍,以及心血管疾病。
查看更多