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4-Aethyl-1,2-dimethylimidazol | 37455-69-9

中文名称
——
中文别名
——
英文名称
4-Aethyl-1,2-dimethylimidazol
英文别名
4-ethyl-1,2-dimethyl-1H-imidazole;4-Ethyl-1,2-dimethylimidazole
4-Aethyl-1,2-dimethylimidazol化学式
CAS
37455-69-9
化学式
C7H12N2
mdl
——
分子量
124.186
InChiKey
GEFNFZTUZOXURZ-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):
    1.2
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • 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

文献信息

  • [EN] CXCR4 RECEPTOR ANTAGONISTS<br/>[FR] ANTAGONISTES DU RÉCEPTEUR CXCR4
    申请人:PROXIMAGEN LTD
    公开号:WO2012049277A1
    公开(公告)日:2012-04-19
    The compounds of formula (I) are antagonists of the CXCR4 receptor Wherein R1 , X, Y and R2 are as defined in the claims.
    式(I)的化合物是CXCR4受体的拮抗剂,其中R1、X、Y和R2如权利要求中所定义。
  • SUBSTITUTED N-HETEROCYCLYL- AND N-HETEROARYL-TETRAHYDROPYRIMIDINONES AND THE SALTS THEREOF, AND THE USE OF SAME AS HERBICIDAL ACTIVE SUBSTANCES
    申请人:Bayer Aktiengesellschaft
    公开号:US20200390100A1
    公开(公告)日:2020-12-17
    The present invention relates to substituted N-heterocyclyl- and N-heteroaryltetrahydropyrimidinones of the general formula (I) or salts thereof, where the radicals in the general formula (I) correspond to the definitions given in the description, and to the use thereof as herbicides, in particular for controlling broad-leaved weeds and/or weed grasses in crops of useful plants and/or as plant growth regulators for influencing the growth of crops of useful plants.
    本发明涉及通式(I)或其盐的取代N-杂环烷基和N-杂芳基四氢嘧啶酮,其中通式(I)中的基团对应于描述中给出的定义,并将其用作除草剂,特别是用于控制作物中的阔叶杂草和/或杂草草,并/或作为植物生长调节剂,以影响作物的生长。
  • TRICYCLIC HETEROCYCLIC COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF
    申请人:Babu Srinivasan
    公开号:US20110201593A1
    公开(公告)日:2011-08-18
    The invention provides novel compounds of formula I having the general formula: wherein R 1 , R 2 , R 3 , X and Y are as described herein. Accordingly, the compounds may be provided in pharmaceutically acceptable compositions and used for the treatment of immunological or hyperproliferative disorders.
    本发明提供了具有以下一般式的新化合物I: 其中R1、R2、R3、X和Y如本文所述。因此,这些化合物可以在药学上可接受的组合物中提供,并用于治疗免疫或过度增生性疾病。
  • CARBON DIOXIDE ABSORBENTS
    申请人:Lee Ki Chun
    公开号:US20110214566A1
    公开(公告)日:2011-09-08
    The present invention relates to a carbon dioxide absorbent. In particular, the present invention relates to a carbon dioxide absorbent comprising an ionic liquid, amine and glycol. Since the carbon dioxide absorbent of the present invention can retain excellent CO 2 absorption capacity despite repetitive regenerations at low temperature, it can reduce energy consumption and a loss of absorbents used, and therefore, can be effectively used for a process of collecting carbon dioxide from exhaust gas and natural gas and separating the same.
    本发明涉及一种二氧化碳吸收剂。具体而言,本发明涉及一种包含离子液体、胺和乙二醇二氧化碳吸收剂。由于本发明的二氧化碳吸收剂可以在低温下重复再生并保持优异的CO2吸收能力,因此可以降低能源消耗和吸收剂的损失,因此可以有效地用于收集废气和天然气中的二氧化碳并将其分离的过程。
  • QUINOLINONE-PYRAZOLONE M1 RECEPTOR POSITIVE ALLOSTERIC MODULATORS
    申请人:Beshore Douglas C.
    公开号:US20120196845A1
    公开(公告)日:2012-08-02
    The present invention is directed to quinolinone-pyrazolone compounds of formula (I) which are M1 receptor positive allosteric modulators and that are useful in the treatment of diseases in which the M1 receptor is involved, such as Alzheimer's disease, schizophrenia, pain or sleep disorders. The invention is also directed to pharmaceutical compositions comprising the compounds, and to the use of the compounds and compositions in the treatment of diseases mediated by the M1 receptor.
    本发明涉及公式(I)的喹啉酮-吡唑酮化合物,它们是M1受体正向变构调节剂,可用于治疗M1受体参与的疾病,如阿尔茨海默病、精神分裂症、疼痛或睡眠障碍。本发明还涉及包括上述化合物的制药组合物,以及在治疗M1受体介导的疾病中使用上述化合物和组合物的方法。
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