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

methyl 2-oxo-1-(2’-methoxycarbonylethyl)cyclohexanecarboxylate | 106421-32-3

中文名称
——
中文别名
——
英文名称
methyl 2-oxo-1-(2’-methoxycarbonylethyl)cyclohexanecarboxylate
英文别名
3-(1-ethoxycarbonyl-2-oxo-cyclohexyl)-propionic acid methyl ester;(+/-)-1-(2-Methoxycarbonyl-aethyl)-2-oxo-cyclohexancarbonsaeure-aethylester;3-(1-Aethoxycarbonyl-2-oxo-cyclohexyl)-propionsaeure-methylester;Ethyl 1-(3-methoxy-3-oxopropyl)-2-oxocyclohexanecarboxylate;ethyl 1-(3-methoxy-3-oxopropyl)-2-oxocyclohexane-1-carboxylate
methyl 2-oxo-1-(2’-methoxycarbonylethyl)cyclohexanecarboxylate化学式
CAS
106421-32-3
化学式
C13H20O5
mdl
——
分子量
256.299
InChiKey
VSOXFDZMBJAVCX-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:
    170-180 °C(Press: 5 Torr)
  • 密度:
    1.116±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.4
  • 重原子数:
    18
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.77
  • 拓扑面积:
    69.7
  • 氢给体数:
    0
  • 氢受体数:
    5

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

点击查看最新优质反应信息

文献信息

  • Development of new DMAP-related organocatalysts for use in the Michael addition reaction of β-ketoesters in water
    作者:Kyungmin Ko、Keiji Nakano、Shigeru Watanabe、Yoshiyasu Ichikawa、Hiyoshizo Kotsuki
    DOI:10.1016/j.tetlet.2009.04.025
    日期:2009.7
    A general and efficient protocol for the Michael addition reactions of β-ketoesters in pure water has been developed. The reactions are successfully catalyzed by newly designed DMAP-related organocatalysts such as 4-(didecylamino)pyridine, and the desired Michael adducts are obtained in good to high yields
    已经开发出一种在纯水中进行β-酮酸酯的迈克尔加成反应的通用有效方案。通过新设计的DMAP相关有机催化剂(例如4-(十二烷基氨基)吡啶)成功催化了反应,并以高收率或高收率获得了所需的迈克尔加合物
  • A study on the phase transfer catalysed Michael addition
    作者:Enrique Díez-Barra、Antonio de la Hoz、Sonia Merino、Ana Rodríguez、Prado Sánchez-Verdú
    DOI:10.1016/s0040-4020(97)10391-x
    日期:1998.2
    Solvent-free and liquid-liquid PTC conditions have been used for the Michael addition of several enolates to methyl vinyl ketone, chalcone and methyl acrylate. The solvent-free technique affords high yields whereas the liquid-liquid procedure is less efficient but allows enantioselective reactions.
    已经使用无溶剂和液-液PTC条件将几种烯酸酯迈克尔加成到甲基乙烯基酮,查尔酮和丙烯酸甲酯中。无溶剂技术可提供高收率,而液-液法效率较低,但允许对映选择性反应。
  • Efficient Organocatalytic Michael Addition Reaction of β−Ketoesters under High Pressure
    作者:Hiyoshizo Kotsuki、Maya Moritaka、Keiji Nakano
    DOI:10.3987/com-13-12818
    日期:——
    The Michael addition reaction of beta-ketoesters was efficiently promoted by a cooperative dual catalyst system composed by DMAP and thiourea A under high-pressure conditions (0.8 GPa) in toluene. The expected relatively congested adducts of 1,5-dicarbonyl compounds were prepared in high to excellent yield.
  • Banerjee; Bhattacharyya, Journal of the Indian Chemical Society, 1958, vol. 35, p. 467,473
    作者:Banerjee、Bhattacharyya
    DOI:——
    日期:——
查看更多