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6-Bromo-3-(3,5-dibromo-4-hydroxyphenyl)-7-methoxychromen-4-one | 1233944-00-7

中文名称
——
中文别名
——
英文名称
6-Bromo-3-(3,5-dibromo-4-hydroxyphenyl)-7-methoxychromen-4-one
英文别名
——
6-Bromo-3-(3,5-dibromo-4-hydroxyphenyl)-7-methoxychromen-4-one化学式
CAS
1233944-00-7
化学式
C16H9Br3O4
mdl
——
分子量
504.957
InChiKey
YTIRJYMPGJRFNL-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):
    4.9
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    脒基硫脲6-Bromo-3-(3,5-dibromo-4-hydroxyphenyl)-7-methoxychromen-4-onesodium methylate 作用下, 以 甲醇 为溶剂, 反应 5.0h, 以54%的产率得到1-[4-(5-bromo-2-hydroxy-4-methoxyphenyl)-5-(3,5-dibromo-4-hydroxyphenyl)pyrimidin-2-yl]thiourea
    参考文献:
    名称:
    One-Step Synthesis of 1-(4,5-Diphenylpyrimidin-2-yl)thiourea
    摘要:
    AbstractA simple and straightforward methodology toward the synthesis of novel 1‐(4,5‐diphenylpyrimidin‐2‐yl)thiourea has been developed by a one‐step reaction of isoflavones with amidinothiourea. A series of 16 new compounds was synthesized. All compounds were characterized by FT‐IR, NMR, and elemental analysis. The structure of a typical compound was established by X‐ray diffraction. A variety of substrates can participate in the process with good yields and high purities, making this methodology suitable for library synthesis in drug discovery.
    DOI:
    10.1002/hlca.200900438
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文献信息

  • One-Step Synthesis of 1-(4,5-Diphenylpyrimidin-2-yl)thiourea
    作者:Wen-Yong Han、Zun-Ting Zhang、Ying-Chun Zhang、Dong Xue、Gang Li
    DOI:10.1002/hlca.200900438
    日期:——
    AbstractA simple and straightforward methodology toward the synthesis of novel 1‐(4,5‐diphenylpyrimidin‐2‐yl)thiourea has been developed by a one‐step reaction of isoflavones with amidinothiourea. A series of 16 new compounds was synthesized. All compounds were characterized by FT‐IR, NMR, and elemental analysis. The structure of a typical compound was established by X‐ray diffraction. A variety of substrates can participate in the process with good yields and high purities, making this methodology suitable for library synthesis in drug discovery.
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