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4-[3-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-phenol | 748771-37-1

中文名称
——
中文别名
——
英文名称
4-[3-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-phenol
英文别名
4-[3-(4-Fluorophenyl)-1,2,4-oxadiazol-5-yl]phenol;4-[3-(4-fluorophenyl)-1,2,4-oxadiazol-5-yl]phenol
4-[3-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-phenol化学式
CAS
748771-37-1
化学式
C14H9FN2O2
mdl
——
分子量
256.236
InChiKey
CNMXFUVEVGUGOF-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):
    3.4
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    59.2
  • 氢给体数:
    1
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    1-(3-氯丙基)-4-甲基哌嗪4-[3-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-phenolpotassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 1-(3-{4-[3-(4-Fluoro-phenyl)-[1,2,4]oxadiazol-5-yl]-phenoxy}-propyl)-4-methyl-piperazine
    参考文献:
    名称:
    Synthesis and structure–activity relationships of 3,5-diarylisoxazoles and 3,5-diaryl-1,2,4-oxadiazoles, novel classes of small molecule interleukin-8 (IL-8) receptor antagonists
    摘要:
    A novel series of 3,5-diarylisoxazole and 3,5-diaryl-1,2,4-oxadiazole IL-8 antagonists has been identified. These compounds exhibit activity in an IL-8 binding assay as well as in a functional assay of IL-8 induced elastase release from neutrophils. In addition, one of the compounds exhibits oral activity in a rat adjuvant arthritis model. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.05.080
  • 作为产物:
    参考文献:
    名称:
    Synthesis and structure–activity relationships of 3,5-diarylisoxazoles and 3,5-diaryl-1,2,4-oxadiazoles, novel classes of small molecule interleukin-8 (IL-8) receptor antagonists
    摘要:
    A novel series of 3,5-diarylisoxazole and 3,5-diaryl-1,2,4-oxadiazole IL-8 antagonists has been identified. These compounds exhibit activity in an IL-8 binding assay as well as in a functional assay of IL-8 induced elastase release from neutrophils. In addition, one of the compounds exhibits oral activity in a rat adjuvant arthritis model. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.05.080
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