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4-Fluoro-benzoic acid 3-isopropoxy-4-piperazin-1-yl-phenyl ester | 194738-01-7

中文名称
——
中文别名
——
英文名称
4-Fluoro-benzoic acid 3-isopropoxy-4-piperazin-1-yl-phenyl ester
英文别名
——
4-Fluoro-benzoic acid 3-isopropoxy-4-piperazin-1-yl-phenyl ester化学式
CAS
194738-01-7
化学式
C20H23FN2O3
mdl
——
分子量
358.413
InChiKey
PPGQLZTUDNKWTJ-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):
    3.24
  • 重原子数:
    26.0
  • 可旋转键数:
    5.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    50.8
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

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
  • 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:
    4-Fluoro-benzoic acid 3-isopropoxy-4-piperazin-1-yl-phenyl estersodium hydroxidesodium carbonate 作用下, 以 乙醇乙酸乙酯 为溶剂, 生成 1-[3-[[4-[2-(1-methoxyethoxy)-4-hydroxyphenyl]-1-piperazinyl]methyl]benzoyl]piperidine
    参考文献:
    名称:
    The synthesis and evaluation of the major metabolites of mazapertine
    摘要:
    Several of the key metabolites of mazapertine, a novel antipyschotic agent, were prepared in order to firmly establish their chemical structure and to obtain samples for biological testing, Hydroxymazapertine 3 was synthesized via a multi-step procedure starting from 5-fluoro-2-nitrophenol (8). Alcohol 4 was originally proposed for one of the major metabolites, but the confirmed structure after synthesis was isomer 20. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0960-894x(97)00336-3
  • 作为产物:
    描述:
    3-isopropoxy-4-nitrophenol 在 palladium on activated charcoal 氢气三乙胺 作用下, 以 乙酸乙酯 为溶剂, 生成 4-Fluoro-benzoic acid 3-isopropoxy-4-piperazin-1-yl-phenyl ester
    参考文献:
    名称:
    The synthesis and evaluation of the major metabolites of mazapertine
    摘要:
    Several of the key metabolites of mazapertine, a novel antipyschotic agent, were prepared in order to firmly establish their chemical structure and to obtain samples for biological testing, Hydroxymazapertine 3 was synthesized via a multi-step procedure starting from 5-fluoro-2-nitrophenol (8). Alcohol 4 was originally proposed for one of the major metabolites, but the confirmed structure after synthesis was isomer 20. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0960-894x(97)00336-3
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