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4-{[(E)-1-(4-Fluoro-benzyl)-1H-benzoimidazol-2-ylimino]-methyl}-2-methoxy-phenol | 144836-20-4

中文名称
——
中文别名
——
英文名称
4-{[(E)-1-(4-Fluoro-benzyl)-1H-benzoimidazol-2-ylimino]-methyl}-2-methoxy-phenol
英文别名
——
4-{[(E)-1-(4-Fluoro-benzyl)-1H-benzoimidazol-2-ylimino]-methyl}-2-methoxy-phenol化学式
CAS
144836-20-4
化学式
C22H18FN3O2
mdl
——
分子量
375.402
InChiKey
UPWOKWKWTGADRX-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):
    4.69
  • 重原子数:
    28.0
  • 可旋转键数:
    5.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    59.64
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    1-substituted 2-benzylaminobenzimidazole derivatives: compounds with H1-antihistaminic activity
    摘要:
    The preparation of 1-substituted 2-benzylaminobenzimidazole derivatives 13-24 is described. Although these compounds have a different structure from the general structure I of antihistamines, they showed some antihistaminic activity (pA2:5-7) when tested in vitro on guinea pig ileum. The introduction of an additional basic centre as in the Mannich bases 25-27 did not cause any improvement of activity. All the compounds tested proved to be inactive in in vivo induced passive cutaneous anaphylaxis (PCA) and cutaneous vasopermeability in rats.
    DOI:
    10.1016/0223-5234(92)90153-r
  • 作为产物:
    描述:
    香草醛1-(4-氟苯基甲基)-2-氨基苯并咪唑甲苯 为溶剂, 反应 15.0h, 以49%的产率得到4-{[(E)-1-(4-Fluoro-benzyl)-1H-benzoimidazol-2-ylimino]-methyl}-2-methoxy-phenol
    参考文献:
    名称:
    1-substituted 2-benzylaminobenzimidazole derivatives: compounds with H1-antihistaminic activity
    摘要:
    The preparation of 1-substituted 2-benzylaminobenzimidazole derivatives 13-24 is described. Although these compounds have a different structure from the general structure I of antihistamines, they showed some antihistaminic activity (pA2:5-7) when tested in vitro on guinea pig ileum. The introduction of an additional basic centre as in the Mannich bases 25-27 did not cause any improvement of activity. All the compounds tested proved to be inactive in in vivo induced passive cutaneous anaphylaxis (PCA) and cutaneous vasopermeability in rats.
    DOI:
    10.1016/0223-5234(92)90153-r
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