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3-甲氧基-5-甲基苯乙酮 | 43113-94-6

中文名称
3-甲氧基-5-甲基苯乙酮
中文别名
1-(3-甲氧基-5-甲基-苯基)-乙酮
英文名称
3-methoxy-5-methylacetophenone
英文别名
3-Methoxy-5-methyl-acetophenon;1-(3-Methoxy-5-methylphenyl)ethanone
3-甲氧基-5-甲基苯乙酮化学式
CAS
43113-94-6
化学式
C10H12O2
mdl
——
分子量
164.204
InChiKey
UXJJSOPJKWZHHY-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):
    1.9
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2914509090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H315,H319,H335

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    磷酰基乙酸三乙酯3-甲氧基-5-甲基苯乙酮 在 sodium hydride 、 lithium aluminium tetrahydride 作用下, 以 四氢呋喃乙醚 为溶剂, 反应 9.5h, 生成 3-(3-methoxy-(E)-5-methylphenyl)but-2-en-1-ol 、
    参考文献:
    名称:
    The First Total Synthesis of (±)-γ-Herbertenol, a Herbertene Isolated from a Non-Herbertus Source
    摘要:
    芳香性倍半萜(±)-γ-赫贝特醇的结构通过全合成得到了确认,该化合物是从非赫贝特斯来源分离出的首个赫贝坦,合成过程中采用了克莱森重排和环闭合复分解反应。
    DOI:
    10.1055/s-2006-950355
  • 作为产物:
    参考文献:
    名称:
    The First Total Synthesis of (±)-γ-Herbertenol, a Herbertene Isolated from a Non-Herbertus Source
    摘要:
    芳香性倍半萜(±)-γ-赫贝特醇的结构通过全合成得到了确认,该化合物是从非赫贝特斯来源分离出的首个赫贝坦,合成过程中采用了克莱森重排和环闭合复分解反应。
    DOI:
    10.1055/s-2006-950355
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文献信息

  • FLUORINATED SULFONATE ESTERS OF ARYL KETONES FOR NON-IONIC PHOTO-ACID GENERATORS
    申请人:International Business Machines Corporation
    公开号:US20180046077A1
    公开(公告)日:2018-02-15
    Non-ionic photo-acid generating (PAG) compounds were prepared that contain an aryl ketone group having a perfluorinated substituent alpha to the ketone carbonyl. The non-polymeric PAGs release a sulfonic acid when exposed to high energy radiation such as deep UV or extreme UV light. The photo-generated sulfonic acid has a low diffusion rate in an exposed resist layer subjected to a post-exposure bake (PEB) at 100° C. to 150° C., resulting in formation of good line patterns after development. At higher temperatures, the PAGs can also undergo a thermal reaction to form a sulfonic acid. The perfluorinated substituent provides improved thermal stability and hydrolytic/nucleophilic stability.
    非离子型光生酸(PAG)化合物被制备出来,它们含有一个含有全氟取代基的芳酮基团,该取代基位于酮羰基的α位置。这些非聚合PAGs在暴露于高能辐射,如深紫外或极紫外光时,会释放出磺酸。在100°C至150°C的后曝光烘烤(PEB)下,光生成的磺酸在暴露的抵抗层中具有较低的扩散速率,从而在开发后形成良好的线条图案。在较高温度下,PAGs也可以通过热反应形成磺酸。全氟取代基提供了改善的热稳定性和水解/亲核稳定性。
  • ISOQUINOLINE COMPOUNDS, A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:LES LABORATOIRES SERVIER
    公开号:US20170137385A1
    公开(公告)日:2017-05-18
    A compound of formula (I): wherein the substituents are as defined in the description. Medicinal products containing the same which are useful in treating or preventing pathologies which are the result of activation of the RhoA/ROCK pathway and phosphorylation of the myosin light chain.
    式(I)的化合物:其中取代基如描述中所定义。含有相同化合物的药品,可用于治疗或预防由RhoA/ROCK途径的激活和肌球蛋白轻链的磷酸化所导致的病理。
  • CHEMICAL COMPOUNDS
    申请人:Campbell Leonie
    公开号:US20080171734A1
    公开(公告)日:2008-07-17
    The invention relates to a novel group of compounds of Formula (I) or a salt thereof: wherein R 1 , A and HET-1 are as described in the specification, which may be useful in the treatment or prevention of a disease or medical condition mediated through glucokinase (GLK) such as type 2 diabetes. The invention also relates to pharmaceutical compositions comprising said compounds, methods of treatment of diseases mediated by GLK using said compounds and methods for preparing compounds of Formula (I).
    这项发明涉及一类新型化合物,其化学式为(I)或其盐:其中R1、A和HET-1如规范中所述,可能在通过葡萄糖激酶(GLK)介导的疾病或医疗状况的治疗或预防中有用,例如2型糖尿病。该发明还涉及包括所述化合物的药物组合物,使用所述化合物治疗由GLK介导的疾病的方法,以及制备化合物(I)的方法。
  • NON-IONIC LOW DIFFUSING PHOTO-ACID GENERATORS
    申请人:International Business Machines Corporation
    公开号:US20180044284A1
    公开(公告)日:2018-02-15
    Non-ionic photo-acid generating (PAG) compounds were prepared that contain an aryl ketone group. The disclosed non-polymeric PAGs release a strong sulfonic acid when exposed to high energy radiation such as deep UV or extreme UV light. The photo-generated sulfonic acid has a low diffusion rate in an exposed resist layer subjected to a post-exposure bake (PEB) at 100° C. to 150° C., resulting in formation of good line patterns after development. At higher temperatures, the PAGs undergo a thermal reaction to form a sulfonic acid.
    制备了含芳基酮基团的非离子光酸发生(PAG)化合物。揭示的非聚合物PAG在暴露于高能辐射(如深紫外或极紫外光)时释放出强磺酸。光生磺酸在经过后曝光烘烤(PEB)处理(在100°C至150°C下)的受暴露光阻层中具有低扩散速率,从而在显影后形成良好的线条图案。在较高温度下,PAG会发生热反应形成磺酸。
  • Chemical Compounds
    申请人:Martin Nathaniel George
    公开号:US20080318968A1
    公开(公告)日:2008-12-25
    The invention relates to a novel group of compounds of Formula (I) or a salt thereof: wherein R 1 , R 2 , R 3 , n, A and HET-1 are as described in the specification, which may be useful in the treatment or prevention of a disease or medical condition mediated through glucokinase (GLK) such as type 2 diabetes. The invention also relates to pharmaceutical compositions comprising said compounds, methods of treatment of diseases mediated by GLK using said compounds and methods for preparing compounds of Formula (I).
    本发明涉及一类新的化合物组,其公式为(I)或其盐: 其中R1、R2、R3、n、A和HET-1如规范所述,可能在治疗或预防通过葡萄糖激酶(GLK)介导的疾病或医疗状况,如2型糖尿病中有用。本发明还涉及包括上述化合物的制药组合物,使用上述化合物治疗GLK介导的疾病的方法以及制备公式(I)化合物的方法。
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