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Methyl 2-(4-chlorobenzoyl)-2-(hydroxymethyl)propanoate | 131825-43-9

中文名称
——
中文别名
——
英文名称
Methyl 2-(4-chlorobenzoyl)-2-(hydroxymethyl)propanoate
英文别名
methyl 2-methyl-2-hydroxymethyl-3-(4-chlorophenyl)-3-keto-propanoate;methyl 3-(4-chlorophenyl)-2-(hydroxymethyl)-2-methyl-3-oxopropanoate
Methyl 2-(4-chlorobenzoyl)-2-(hydroxymethyl)propanoate化学式
CAS
131825-43-9
化学式
C12H13ClO4
mdl
——
分子量
256.686
InChiKey
LNEDCSACIDUSAS-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):
    2
  • 重原子数:
    17
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 氢受体数:
    4

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
  • 下游产品
    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:
    Methyl 2-(4-chlorobenzoyl)-2-(hydroxymethyl)propanoatesodium acetate一水合肼溶剂黄146三乙胺 作用下, 以 甲醇二氯甲烷甲苯 为溶剂, 反应 10.0h, 生成 methyl 5-(4-chlorophenyl)-2-[(4-methoxyphenyl)carbamoyl]-4-methyl-3H-pyrazole-4-carboxylate
    参考文献:
    名称:
    Quantitative structure-activity relationships of insecticidal pyrazolines
    摘要:
    AbstractMethyl 3‐(4‐chlorophenyl)‐4‐methyl‐1‐[N‐(4‐substituted pheny1)carba‐moy1]‐2‐pyrazoline‐4‐carboxylates and related compounds were prepared. Their convulsant activity was determined as the minimum dose required to bring about the symptom within 1 h after injection against male adult American cockroaches, Periplaneta americana (L.). Insecticidal activity with metabolic inhibitors for oxidation and hydrolysis was measured 24 h after injection of the test compounds. Variations in each of the activities were analysed by using physicochemical substituent parameters and regression analysis. The findings indicated that the greater the hydrophobicity and the more the electron‐withdrawing property of the substituents, the higher were the activities. Variations in each of the two activities were parabolically related to the STERIMOL width parameter with an optimum value of about zero.
    DOI:
    10.1002/ps.2780420406
  • 作为产物:
    描述:
    4-氯苯丙酮吡啶苄基三甲基氢氧化铵 、 sodium hydride 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 2.0h, 生成 Methyl 2-(4-chlorobenzoyl)-2-(hydroxymethyl)propanoate
    参考文献:
    名称:
    Quantitative structure-activity relationships of insecticidal pyrazolines
    摘要:
    AbstractMethyl 3‐(4‐chlorophenyl)‐4‐methyl‐1‐[N‐(4‐substituted pheny1)carba‐moy1]‐2‐pyrazoline‐4‐carboxylates and related compounds were prepared. Their convulsant activity was determined as the minimum dose required to bring about the symptom within 1 h after injection against male adult American cockroaches, Periplaneta americana (L.). Insecticidal activity with metabolic inhibitors for oxidation and hydrolysis was measured 24 h after injection of the test compounds. Variations in each of the activities were analysed by using physicochemical substituent parameters and regression analysis. The findings indicated that the greater the hydrophobicity and the more the electron‐withdrawing property of the substituents, the higher were the activities. Variations in each of the two activities were parabolically related to the STERIMOL width parameter with an optimum value of about zero.
    DOI:
    10.1002/ps.2780420406
  • 作为试剂:
    描述:
    methyl 3-(4-chlorophenyl)-2-methyl-3-oxopropanoate聚合甲醛吡啶盐酸 在 ice 、 Brine 、 magnesium sulfateMethyl 2-(4-chlorobenzoyl)-2-(hydroxymethyl)propanoate 作用下, 以 甲醇乙醚 为溶剂, 反应 2.0h, 以affords 1100 g (100%) of a red oil, methyl 2-methyl-2-hydroxymethyl-3-(4-chlorophenyl)-3-keto-propanoate的产率得到Methyl 2-(4-chlorobenzoyl)-2-(hydroxymethyl)propanoate
    参考文献:
    名称:
    N-aryl-3-aryl-4,5-dihydro-1H-pyrazole-1-carboxamides and methods of
    摘要:
    本发明涉及一种新型的N-芳基-3-芳基-4,5-二氢-1H-吡唑-1-羧酰胺化合物,其作为杀虫剂有用,包含这些化合物的组合物,控制害虫的方法和制备这些化合物的方法。
    公开号:
    US04863947A1
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文献信息

  • US4863947A
    申请人:——
    公开号:US4863947A
    公开(公告)日:1989-09-05
  • Quantitative structure-activity relationships of insecticidal pyrazolines
    作者:Riaz Hasan、Keiichiro Nishimura、Tamio Ueno
    DOI:10.1002/ps.2780420406
    日期:1994.12
    AbstractMethyl 3‐(4‐chlorophenyl)‐4‐methyl‐1‐[N‐(4‐substituted pheny1)carba‐moy1]‐2‐pyrazoline‐4‐carboxylates and related compounds were prepared. Their convulsant activity was determined as the minimum dose required to bring about the symptom within 1 h after injection against male adult American cockroaches, Periplaneta americana (L.). Insecticidal activity with metabolic inhibitors for oxidation and hydrolysis was measured 24 h after injection of the test compounds. Variations in each of the activities were analysed by using physicochemical substituent parameters and regression analysis. The findings indicated that the greater the hydrophobicity and the more the electron‐withdrawing property of the substituents, the higher were the activities. Variations in each of the two activities were parabolically related to the STERIMOL width parameter with an optimum value of about zero.
  • N-aryl-3-aryl-4,5-dihydro-1H-pyrazole-1-carboxamides and methods of
    申请人:Rohm and Haas
    公开号:US04863947A1
    公开(公告)日:1989-09-05
    This invention relates to novel N-aryl-3-aryl-4,5-dihydro-1H-pyrazole-1-carboxamide compounds which are useful as pesticides, compositions containing those compounds, methods of controlling pests and processes for preparing these compounds.
    本发明涉及新颖的N-芳基-3-芳基-4,5-二氢-1H-吡唑-1-甲酰胺化合物,这些化合物作为农药具有实用性,包含这些化合物的组合物,控制害虫的方法以及制备这些化合物的工艺。
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