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Piperidine, 1-[2-[4-(2H-1-benzopyran-2-yl)phenoxy]ethyl]- | 189290-20-8

中文名称
——
中文别名
——
英文名称
Piperidine, 1-[2-[4-(2H-1-benzopyran-2-yl)phenoxy]ethyl]-
英文别名
1-[2-[4-(2H-chromen-2-yl)phenoxy]ethyl]piperidine
Piperidine, 1-[2-[4-(2H-1-benzopyran-2-yl)phenoxy]ethyl]-化学式
CAS
189290-20-8
化学式
C22H25NO2
mdl
——
分子量
335.446
InChiKey
BHVFELWJKSAVQZ-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):
    4.8
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    21.7
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2',4-dihydroxychalcone 在 sodium tetrahydroborate 、 potassium carbonate 作用下, 以 乙醇丙酮 为溶剂, 生成 Piperidine, 1-[2-[4-(2H-1-benzopyran-2-yl)phenoxy]ethyl]-
    参考文献:
    名称:
    Synthesis and post-coital contraceptive activity of a new series of substituted 2,3-diaryl-2H-1-benzopyrans
    摘要:
    A series of substituted 2,3-diaryl-2H-1-benzopyrans have been synthesized and screened for their post-coital contraceptive activity in rats. Most of the compounds showed 100% inhibition in a single day schedule at a dose level of 1.0 mg/kg. Compound 32 was found to be the most active with a minimum effective dose (MED) of 0.2 mg/kg in single day testing. Further, it also showed high antiestrogenic activity and is devoid of any agonistic activity.
    DOI:
    10.1016/s0223-5234(97)87540-x
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文献信息

  • Synthesis and post-coital contraceptive activity of a new series of substituted 2,3-diaryl-2H-1-benzopyrans
    作者:K Hajela、RS Kapil
    DOI:10.1016/s0223-5234(97)87540-x
    日期:1997.1
    A series of substituted 2,3-diaryl-2H-1-benzopyrans have been synthesized and screened for their post-coital contraceptive activity in rats. Most of the compounds showed 100% inhibition in a single day schedule at a dose level of 1.0 mg/kg. Compound 32 was found to be the most active with a minimum effective dose (MED) of 0.2 mg/kg in single day testing. Further, it also showed high antiestrogenic activity and is devoid of any agonistic activity.
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