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1-Methoxy-2-methyl-4-(trifluoromethoxy)benzene | 887266-88-8

中文名称
——
中文别名
——
英文名称
1-Methoxy-2-methyl-4-(trifluoromethoxy)benzene
英文别名
——
1-Methoxy-2-methyl-4-(trifluoromethoxy)benzene化学式
CAS
887266-88-8
化学式
C9H9F3O2
mdl
MFCD04972926
分子量
206.16
InChiKey
UDUQEVKEBPIJJE-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:
    187.6±35.0 °C(Predicted)
  • 密度:
    1.211±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • 8-AZABICYCLO[3.2.1]OCTANE-8-CARBOXAMIDE DERIVATIVE
    申请人:Horiuchi Yoshihiro
    公开号:US20120225876A1
    公开(公告)日:2012-09-06
    Disclosed is a compound represented by formula (1) or a pharmacologically acceptable salt thereof (In the formula, A represents a group that is represented by formula (A-1); R 1a and R 1b may be the same or different and each independently represents a C 1-6 alkyl group which may be substituted by one to three halogen atoms; m and n each independently represents an integer of 0-5; X 1 represents a hydroxyl group or an aminocarbonyl group; Z 1 represents a single bond or the like; and R 2 represents an optionally substituted C 1-6 alkyl group, an optionally substituted C 6-10 aryl group or the like.)
    公开了一种由公式(1)表示的化合物或其药理可接受的盐(在公式中,A代表由公式(A-1)表示的基团;R1a和R1b可以相同或不同,每个独立地表示一个可以由一个到三个卤素原子取代的C1-6烷基;m和n各自独立地表示0-5之间的整数;X1代表羟基或氨基甲酰基;Z1代表单键等;R2代表一个可选地取代的C1-6烷基,一个可选地取代的C6-10芳基等)。
  • Nitrogen-containing heterocyclic compound and use thereof
    申请人:Ikeura Yoshinori
    公开号:US20090156572A1
    公开(公告)日:2009-06-18
    The present invention relates to a compound represented by the formula wherein ring A is a nitrogen-containing heterocycle optionally further having substituent(s), ring B is an aromatic ring optionally having substituent(s), ring C is a cyclic group optionally having substituent(s), R 1 is a hydrogen atom, a hydrocarbon group optionally having substituent(s), an acyl group, a heterocyclic group optionally having substituent(s) or an amino group optionally having substituent(s), R 2 is an optionally halogenated C 1-6 alkyl group, m and n are each an integer of 0 to 5, m+n is an integer of 2 to 5, and is a single bond or a double bond, or a salt thereof and the like. Since the compound has a superior tachykinin receptor antagonistic action, and is useful as an agent for the prophylaxis or treatment of various diseases such as lower urinary tract diseases, gastrointestinal diseases, central nervous system diseases and the like.
    本发明涉及一种由下式表示的化合物:其中环A是含氮杂环,可选择地进一步具有取代基,环B是芳香环,可选择地具有取代基,环C是环状基团,可选择地具有取代基,R1是氢原子,一个碳氢基团,可选择地具有取代基,酰基,一个杂环基团,可选择地具有取代基或一个氨基团,可选择地具有取代基,R2是可选择卤代的C1-6烷基基团,m和n分别是0到5的整数,m+n是2到5的整数,是单键或双键,或其盐等。由于该化合物具有优越的催吐肽受体拮抗作用,可用作预防或治疗多种疾病的药物,如下尿道疾病、胃肠道疾病、中枢神经系统疾病等。
  • SUBSTITUTED BICYCLIC PYRIMIDONE DERIVATIVES
    申请人:CHEREZE Nathalie
    公开号:US20090036427A1
    公开(公告)日:2009-02-05
    A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof: Wherein Y, Z, R1, R2, R3, R4, R5, R6, R7, n, m, and o are as described herein. The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β, such as Alzheimer disease.
    一种由式(I)表示的吡啶酮衍生物或其盐、溶剂或水合物:其中Y、Z、R1、R2、R3、R4、R5、R6、R7、n、m和o如所述。本发明还涉及一种药物,其包含所述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β异常活性引起的神经退行性疾病,如阿尔茨海默病。
  • Benzimidazole derivatives and their use as protein kinases inhibitors
    申请人:Berdini Valerio
    公开号:US20070135477A1
    公开(公告)日:2007-06-14
    The invention provides compounds of the formula (1): The compounds have activity against cyclin depdenent kinases, glycogen synthase kinase and Auroa kinases and are therefore useful to treat cancer and viral diseases.
    该发明提供了式(1)的化合物: 这些化合物具有对环素依赖性激酶、糖原合成酶激酶和Auroa激酶的活性,因此可用于治疗癌症和病毒性疾病。
  • DIAMINOTRIAZOLES USEFUL AS INHIBITORS OF PROTEIN KINASES
    申请人:Pierce C. Albert
    公开号:US20080014189A1
    公开(公告)日:2008-01-17
    The present invention relates to inhibitors of protein kinases. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders.
    本发明涉及蛋白激酶抑制剂。该发明还提供了包含本发明化合物的药物组合物以及使用该组合物治疗各种疾病的方法。
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