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

2-环丙基-1-甲基-1H-咪唑 | 871507-60-7

中文名称
2-环丙基-1-甲基-1H-咪唑
中文别名
——
英文名称
2-cyclopropyl-1-methyl-1H-imidazole
英文别名
2-cyclopropyl-1-methylimidazole
2-环丙基-1-甲基-1H-咪唑化学式
CAS
871507-60-7
化学式
C7H10N2
mdl
——
分子量
122.17
InChiKey
CVWGFCNSHOZVQS-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:
    259.3±9.0 °C(Predicted)
  • 密度:
    1.19±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • HETEROARYL CARBOXAMIDE COMPOUNDS AS INHIBITORS OF RIPK2
    申请人:Boehringer Ingelheim International GmbH
    公开号:US20180072717A1
    公开(公告)日:2018-03-15
    The present invention relates to compounds of formula (I): or pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , X, Y, and HET are as defined herein. The invention also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes
    本发明涉及以下式(I)的化合物: 或其药学上可接受的盐,其中R 1 ,R 2 ,X,Y和HET如本文所定义。该发明还涉及包含这些化合物的药物组合物,使用这些化合物治疗各种疾病和紊乱的方法,制备这些化合物的过程以及在这些过程中有用的中间体。
  • Process for making cytokine inhibiting compounds containing 4- and 5-imidazolyl rings and the intermediates thereof
    申请人:Boehringer Ingelheim International GmbH
    公开号:US07858804B2
    公开(公告)日:2010-12-28
    Disclosed are processes for making compounds containing 4- and 5-imidazolyl rings, also disclosed are the intermediates useful in the processes disclosed herein.
    本发明揭示了制备含有4-和5-咪唑基环的化合物的过程,同时揭示了在本发明中有用的中间体。
  • INHIBITORS OF POLO-LIKE KINASE
    申请人:Galemmo Robert A.
    公开号:US20110212942A1
    公开(公告)日:2011-09-01
    The present invention provides compounds having a structure according to Formula (I): or a salt or solvate thereof, wherein ring A, X, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are defined herein. The invention further provides pharmaceutical compositions including the compounds of the invention and methods of making and using the compounds and compositions of the invention, e.g., in the treatment and prevention of various disorders, such as Parkinson's disease.
    本发明提供了具有以下式子(I)结构的化合物,或其盐或溶剂化物,其中环A,X,R1,R2,R3,R4,R5和R6在此被定义。本发明还提供了包括本发明化合物的制药组合物以及使用本发明化合物和组合物的方法,例如在治疗和预防各种疾病,如帕森病中的应用。
  • Process for Making Cytokine Inhibiting Compounds Containing 4- and 5-Imidazolyl Rings and the Intermediates Thereof
    申请人:Frutos Rogelio Perez
    公开号:US20090137815A1
    公开(公告)日:2009-05-28
    Disclosed are processes for making compounds containing 4- and 5-imidazolyl rings, also disclosed are the inter-mediates useful in the processes disclosed herein.
    本发明揭示了制备含有4-和5-咪唑基环的化合物的过程,同时也揭示了本发明中有用的中间体。
  • SUBSTITUTED IMIDAZOLE SALT COMPOUNDS, PREPARATION METHOD THEREFOR, PHARMACEUTICAL COMPOSITION THEREOF, AND APPLICATIONS THEREOF
    申请人:Xiamen Vivohealths Technology Co., Ltd.
    公开号:EP3608312A1
    公开(公告)日:2020-02-12
    Disclosed in the invention are a type of compounds having aldolase selective inhibitory activity, a method for the preparation thereof, a pharmaceutical composition comprising the same, and use of these compounds in the manufacture of a medicament for inhibiting triglyceride and cholesterol synthesis, for reducing fatty acid synthesis, for preventing and/or treating obesity and type II diabetes, for preventing and/or treating tumor, for preventing and/or treating Parkinson's disease, for preventing and/or treating Alzheimer's disease or for prolonging the lifespan of mammals:
    本发明公开了一种具有醛缩酶选择性抑制活性的化合物、其制备方法、包含这些化合物的药物组合物,以及这些化合物在制造用于抑制甘油三酯胆固醇合成、减少脂肪酸合成、预防和/或治疗肥胖症和II型糖尿病、预防和/或治疗肿瘤、预防和/或治疗帕森病、预防和/或治疗阿尔茨海默病或延长哺乳动物寿命的药物中的用途:
查看更多