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methyl 2-[hydroxy(mesitylacetyl)amino]-2-methyl-3-phenylpropanoate | 596806-81-4

中文名称
——
中文别名
——
英文名称
methyl 2-[hydroxy(mesitylacetyl)amino]-2-methyl-3-phenylpropanoate
英文别名
Methyl 2-[hydroxy-[2-(2,4,6-trimethylphenyl)acetyl]amino]-2-methyl-3-phenylpropanoate
methyl 2-[hydroxy(mesitylacetyl)amino]-2-methyl-3-phenylpropanoate化学式
CAS
596806-81-4
化学式
C22H27NO4
mdl
——
分子量
369.461
InChiKey
AHBVHMATYMCAPT-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):
    4
  • 重原子数:
    27
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    66.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    methyl 2-[hydroxy(mesitylacetyl)amino]-2-methyl-3-phenylpropanoatepotassium tert-butylate 、 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 3.0h, 生成 5-Benzyl-4-hydroxy-1-methoxymethoxy-5-methyl-3-(2,4,6-trimethyl-phenyl)-1,5-dihydro-pyrrol-2-one
    参考文献:
    名称:
    Synthesis and insecticidal activity of novel N-oxydihydropyrroles: 4-hydroxy-3-mesityl-1-methoxymethoxy derivatives with various substituents at the 5-position
    摘要:
    This paper reports the synthesis and insecticidal activity of a series of novel 4-hydroxy-3-mesityl-1-methoxymethoxy-1,5-dihydro-2H-pyrrol-2-one derivatives, in which the substituents at the 5-position were varied with a number of alkyl and spirocycloalkyl groups. Investigation of the structure-activity relationships revealed that small alkyl and spirocyclohexyl groups had a favorable effect on the insecticidal activity of these agents against Myzus persicae. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(02)00474-1
  • 作为产物:
    参考文献:
    名称:
    Synthesis and insecticidal activity of novel N-oxydihydropyrroles: 4-hydroxy-3-mesityl-1-methoxymethoxy derivatives with various substituents at the 5-position
    摘要:
    This paper reports the synthesis and insecticidal activity of a series of novel 4-hydroxy-3-mesityl-1-methoxymethoxy-1,5-dihydro-2H-pyrrol-2-one derivatives, in which the substituents at the 5-position were varied with a number of alkyl and spirocycloalkyl groups. Investigation of the structure-activity relationships revealed that small alkyl and spirocyclohexyl groups had a favorable effect on the insecticidal activity of these agents against Myzus persicae. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(02)00474-1
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