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3-bromo-8-quinolinol-5-sulfonic acid | 374563-05-0

中文名称
——
中文别名
——
英文名称
3-bromo-8-quinolinol-5-sulfonic acid
英文别名
3,6-Bromo-8-quinolinol-5-sulfonic acid;3-bromo-8-hydroxyquinoline-5-sulfonic acid
3-bromo-8-quinolinol-5-sulfonic acid化学式
CAS
374563-05-0
化学式
C9H6BrNO4S
mdl
——
分子量
304.121
InChiKey
WPKUSFKZEYQGMN-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):
    1.3
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    95.9
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 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:
    3-bromo-8-quinolinol-5-sulfonic acid氢氧化钾N-溴代丁二酰亚胺(NBS) 作用下, 以 为溶剂, 反应 0.5h, 以56%的产率得到3,7-dibromo-8-quinolinol-5-sulfonic acid
    参考文献:
    名称:
    Preparation and Fungitoxicity of Some Dibromo-8-quinolinols
    摘要:
    2,5-, 3,5-, 3,6-, 3,7-, 4,5-, 5,6-, 5,7-, and 6,7-dibromo-8-quinolinols were prepared and tested against six fungi (Aspergillus niger, Aspergillus oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes) in Sabouraud dextrose broth. Most of the compounds were strongly antifungal, inhibiting five of the fungi below 1 mug/cm(3), but were somewhat less fungitoxic than the corresponding chloro analogues. M. cirinelloides was not inhibited by any of the compounds except 4,5-dibromo-8-quinolinol. This high level of fungitoxicity is attributed to intramolecular synergism.
    DOI:
    10.1007/s007060170071
  • 作为产物:
    描述:
    3-bromo-8-quinolinol硫酸 作用下, 以89%的产率得到3-bromo-8-quinolinol-5-sulfonic acid
    参考文献:
    名称:
    Preparation and Fungitoxicity of Some Dibromo-8-quinolinols
    摘要:
    2,5-, 3,5-, 3,6-, 3,7-, 4,5-, 5,6-, 5,7-, and 6,7-dibromo-8-quinolinols were prepared and tested against six fungi (Aspergillus niger, Aspergillus oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes) in Sabouraud dextrose broth. Most of the compounds were strongly antifungal, inhibiting five of the fungi below 1 mug/cm(3), but were somewhat less fungitoxic than the corresponding chloro analogues. M. cirinelloides was not inhibited by any of the compounds except 4,5-dibromo-8-quinolinol. This high level of fungitoxicity is attributed to intramolecular synergism.
    DOI:
    10.1007/s007060170071
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文献信息

  • Preparation and Fungitoxicity of Some Dibromo-8-quinolinols
    作者:Herman Gershon、Donald D. Clarke、John J. McMahon、Muriel Gershon
    DOI:10.1007/s007060170071
    日期:2001.7
    2,5-, 3,5-, 3,6-, 3,7-, 4,5-, 5,6-, 5,7-, and 6,7-dibromo-8-quinolinols were prepared and tested against six fungi (Aspergillus niger, Aspergillus oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes) in Sabouraud dextrose broth. Most of the compounds were strongly antifungal, inhibiting five of the fungi below 1 mug/cm(3), but were somewhat less fungitoxic than the corresponding chloro analogues. M. cirinelloides was not inhibited by any of the compounds except 4,5-dibromo-8-quinolinol. This high level of fungitoxicity is attributed to intramolecular synergism.
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