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6-(2,5-Dichlorophenyl)-3,4-diphenyl-2-(2-pyridyl)pyrazolo[3,4-d]pyridazin-7-one

中文名称
——
中文别名
——
英文名称
6-(2,5-Dichlorophenyl)-3,4-diphenyl-2-(2-pyridyl)pyrazolo[3,4-d]pyridazin-7-one
英文别名
6-(2,5-dichlorophenyl)-3,4-diphenyl-2-pyridin-2-ylpyrazolo[3,4-d]pyridazin-7-one
6-(2,5-Dichlorophenyl)-3,4-diphenyl-2-(2-pyridyl)pyrazolo[3,4-d]pyridazin-7-one化学式
CAS
——
化学式
C28H17Cl2N5O
mdl
——
分子量
510.382
InChiKey
OHEFYKLXLDEWOS-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):
    6.9
  • 重原子数:
    36
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    63.4
  • 氢给体数:
    0
  • 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

反应信息

  • 作为产物:
    参考文献:
    名称:
    Antibacterial and antifungal activities of new pyrazolo[3,4-d]pyridazin derivatives
    摘要:
    Several new pyrazolo[3,4-d]pyridazin derivatives were prepared by the reaction of two new 1H-pyrazole-3-carboxylic acids and various hydrazines. The compounds were tested for antimicrobial activities against Gram-negative, Gram-positive bacteria and fungi. The compounds named as 7e, f had the highest antimicrobial activities against Gram-negative, Gram-positive bacteria and fungi with minimum inhibitory concentrations in the range of 0.31 to < 0.0024 mg ml(-1). (c) 2005 Elsevier SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2004.12.001
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文献信息

  • Antibacterial and antifungal activities of new pyrazolo[3,4-d]pyridazin derivatives
    作者:Esvet Akbas、Ismet Berber
    DOI:10.1016/j.ejmech.2004.12.001
    日期:2005.4
    Several new pyrazolo[3,4-d]pyridazin derivatives were prepared by the reaction of two new 1H-pyrazole-3-carboxylic acids and various hydrazines. The compounds were tested for antimicrobial activities against Gram-negative, Gram-positive bacteria and fungi. The compounds named as 7e, f had the highest antimicrobial activities against Gram-negative, Gram-positive bacteria and fungi with minimum inhibitory concentrations in the range of 0.31 to < 0.0024 mg ml(-1). (c) 2005 Elsevier SAS. All rights reserved.
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