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

ethyl 2-isonicotinoyl-3-oxobutanoate | 958256-05-8

中文名称
——
中文别名
——
英文名称
ethyl 2-isonicotinoyl-3-oxobutanoate
英文别名
3-oxo-2-(pyridine-4-carbonyl)-butyric acid ethyl ester;Ethyl 2-isonicotinoyl-3-oxobutanoate;ethyl 3-oxo-2-(pyridine-4-carbonyl)butanoate
ethyl 2-isonicotinoyl-3-oxobutanoate化学式
CAS
958256-05-8
化学式
C12H13NO4
mdl
——
分子量
235.24
InChiKey
UREKUPPBQRSXTD-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):
    0.9
  • 重原子数:
    17
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    73.3
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

点击查看最新优质反应信息

文献信息

  • PYRAZOL DERIVATIVES
    申请人:Aebi Johannes
    公开号:US20090029963A1
    公开(公告)日:2009-01-29
    The invention is concerned with novel pyrazol derivatives of formula (I), wherein R 1 , R 2 , R 3 , R 4 , X and Y are as defined herein, as well as physiologically acceptable salts thereof. These compounds are antagonists of CCR-2 receptor and/or CCR-5 receptor and can be used as medicaments.
    这项发明涉及式(I)的新型吡唑衍生物, 其中 R 1 ,R 2 ,R 3 ,R 4 ,X和Y如本文所定义,以及其生理上可接受的盐。这些化合物是CCR-2受体和/或CCR-5受体的拮抗剂,可用作药物。
  • SmCl<sub>3</sub>-Catalyzed <i>C-</i>Acylation of 1,3-Dicarbonyl Compounds and Malononitrile
    作者:Quansheng Shen、Wen Huang、Jialiang Wang、Xigeng Zhou
    DOI:10.1021/ol701961z
    日期:2007.10.1
    A recyclable, convenient, and efficient catalytic system for C-acylation of 1,3-dicarbonyl compounds and malononitrile with acid chlorides has been developed, giving moderate to excellent yields under mild conditions. This is the first catalytic example of such reactions. In addition, by applying this protocol as the key step, 3,5-disubstituted-1H-pyrazole-4-carboxylate can easily be synthesized in
    已开发出一种可回收,方便且有效的催化体系,用于用酰氯对1,3-二羰基化合物和丙二腈进行C-酰化,在温和条件下产生中等至极好的收率。这是这种反应的第一个催化实例。另外,通过将该方案用作关键步骤,可以轻松地以一锅法高收率合成3,5-二取代-1H-吡唑-4-羧酸酯。
  • Pyrazol derivatives
    申请人:Hoffmann-La Roche Inc.
    公开号:US07977358B2
    公开(公告)日:2011-07-12
    The invention is concerned with novel pyrazol derivatives of formula (I), wherein R1, R2, R3, R4, X and Y are as defined herein, as well as physiologically acceptable salts thereof. These compounds are antagonists of CCR-2 receptor and/or CCR-5 receptor and can be used as medicaments.
    本发明涉及公式(I)的新型吡唑衍生物,其中R1、R2、R3、R4、X和Y的定义如本文所述,以及其生理上可接受的盐。这些化合物是CCR-2受体和/或CCR-5受体的拮抗剂,可用作药物。
  • Heterocyclic compounds
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US08865717B2
    公开(公告)日:2014-10-21
    The present invention provides a compound useful as an agent for the prophylaxis or treatment of neurodegenerative disease and the like, or a salt thereof. The present invention relates to a compound represented by the formula wherein each symbol is as defined in the specification, or a salt thereof.
    本发明提供一种化合物及其盐,可用作神经退行性疾病的预防或治疗剂。该化合物的结构式如下所示,其中每个符号的定义在规范中给出。
  • 1-ARYLCARBONYL-4-OXY-PIPERIDINE COMPOUNDS USEFUL FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US20140228373A1
    公开(公告)日:2014-08-14
    The present invention provides a compound useful as an agent for the prophylaxis or treatment of neurodegenerative disease and the like, or a salt thereof. The present invention relates to a compound represented by the formula (I) wherein each symbol is as defined in the specification, or a salt thereof.
    本发明提供了一种化合物及其盐,可用作预防或治疗神经退行性疾病等的药剂。本发明涉及一种由式(I)表示的化合物,其中每个符号如规范中定义的,或其盐。
查看更多