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1-(4-Bromophenyl)-4-(4-fluorophenyl)-2-methyl-pyrrole-3-carboxylic acid

中文名称
——
中文别名
——
英文名称
1-(4-Bromophenyl)-4-(4-fluorophenyl)-2-methyl-pyrrole-3-carboxylic acid
英文别名
1-(4-bromophenyl)-4-(4-fluorophenyl)-2-methylpyrrole-3-carboxylic acid
1-(4-Bromophenyl)-4-(4-fluorophenyl)-2-methyl-pyrrole-3-carboxylic acid化学式
CAS
——
化学式
C18H13BrFNO2
mdl
——
分子量
374.209
InChiKey
VKEFJNOGSWOURX-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):
    4.7
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    42.2
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    描述:
    Ethyl 1-(4-bromophenyl)-4-(4-fluorophenyl)-2-methylpyrrole-3-carboxylatesodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 10.0h, 以78%的产率得到1-(4-Bromophenyl)-4-(4-fluorophenyl)-2-methyl-pyrrole-3-carboxylic acid
    参考文献:
    名称:
    Research on antibacterial and antifungal agents. VIII. synthesis and antimicrobial activity of 1,4-diarylpyrroles
    摘要:
    The synthesis and the antimicrobial activity of 1,4-diarylpyrroles are reported. The obtained data in comparison with pyrrolnitrin show that many acid derivatives 4 exhibit a selective activity against some strains of Candida spp and poor activity against strains of Candida albicans. All ester derivatives 3 are inactive. The results obtained are discussed on the basis of structure-activity relationships.
    DOI:
    10.1016/0223-5234(92)90092-f
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文献信息

  • Research on antibacterial and antifungal agents. VIII. synthesis and antimicrobial activity of 1,4-diarylpyrroles
    作者:GC Porretta、M Biava、R Fioravanti、M Fischetti、C Melino、F Venza、P Bolle、B Tita
    DOI:10.1016/0223-5234(92)90092-f
    日期:1992.10
    The synthesis and the antimicrobial activity of 1,4-diarylpyrroles are reported. The obtained data in comparison with pyrrolnitrin show that many acid derivatives 4 exhibit a selective activity against some strains of Candida spp and poor activity against strains of Candida albicans. All ester derivatives 3 are inactive. The results obtained are discussed on the basis of structure-activity relationships.
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