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(E)-N'-(4-methoxybenzylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide | 1284268-03-6

中文名称
——
中文别名
——
英文名称
(E)-N'-(4-methoxybenzylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide
英文别名
3-(4-chlorophenyl)-N-[(E)-(4-methoxyphenyl)methyleneamino]-1H-pyrazole-5-carboxamide;3-(4-chlorophenyl)-N-[(E)-(4-methoxyphenyl)methylideneamino]-1H-pyrazole-5-carboxamide
(E)-N'-(4-methoxybenzylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide化学式
CAS
1284268-03-6
化学式
C18H15ClN4O2
mdl
——
分子量
354.796
InChiKey
PQTVEBFPTXVCRX-RGVLZGJSSA-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

  • 密度:
    1.32±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    79.4
  • 氢给体数:
    2
  • 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:
    (E)-N'-(4-methoxybenzylidene)-3-(4-chlorophenyl)-1H-pyrazole-5-carbohydrazide氯乙酰氯三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 2.5h, 以47%的产率得到(+/-)-trans-N-(3-chloro-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl)-3-(4-chlorophenyl)-1H-pyrazole-5-carboxamide
    参考文献:
    名称:
    Synthesis, antitubercular and antimicrobial evaluation of 3-(4-chlorophenyl)-4-substituted pyrazole derivatives
    摘要:
    As a part of our research to develop novel antitubercular and antimicrobial agents, a series of 3-(4-chlorophenyl)-4-substituted pyrazoles have been synthesised. These compounds were tested for antitubercular activity in vitro against Mycobacterium tuberculosis H37Rv strain using the BACTEC 460 radiometric system, antifungal activity against a pathogenic strain of fungi and antibacterial activity against grampositive and gram-negative organisms. Among them tested, many compounds showed good to excellent antimicrobial and antitubercular activity. The results suggest that hydrazones, 2-azetidinones and 4-thiazolidinones bearing a core pyrazole scaffold would be potent antimicrobial and antitubercular agents. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.05.063
  • 作为产物:
    参考文献:
    名称:
    Synthesis, antitubercular and antimicrobial evaluation of 3-(4-chlorophenyl)-4-substituted pyrazole derivatives
    摘要:
    As a part of our research to develop novel antitubercular and antimicrobial agents, a series of 3-(4-chlorophenyl)-4-substituted pyrazoles have been synthesised. These compounds were tested for antitubercular activity in vitro against Mycobacterium tuberculosis H37Rv strain using the BACTEC 460 radiometric system, antifungal activity against a pathogenic strain of fungi and antibacterial activity against grampositive and gram-negative organisms. Among them tested, many compounds showed good to excellent antimicrobial and antitubercular activity. The results suggest that hydrazones, 2-azetidinones and 4-thiazolidinones bearing a core pyrazole scaffold would be potent antimicrobial and antitubercular agents. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.05.063
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