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4,6-bis[3-(bromomethyl)-1H-pyrazol-1-yl]pyrimidine | 1439863-93-0

中文名称
——
中文别名
——
英文名称
4,6-bis[3-(bromomethyl)-1H-pyrazol-1-yl]pyrimidine
英文别名
4,6-Bis[3-(bromomethyl)pyrazol-1-yl]pyrimidine
4,6-bis[3-(bromomethyl)-1H-pyrazol-1-yl]pyrimidine化学式
CAS
1439863-93-0
化学式
C12H10Br2N6
mdl
——
分子量
398.06
InChiKey
FNEODOMXNREJEP-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):
    2
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    61.4
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    五溴化磷 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 12.0h, 以46 mg的产率得到4,6-bis[3-(bromomethyl)-1H-pyrazol-1-yl]pyrimidine
    参考文献:
    名称:
    Nucleophilic Substitution on Polyfluorinated Pyridine and Pyrimidine Rings for Construction of Lanthanide Ligands
    摘要:
    The use of nucleophilic substitution of fluoride attached to azaaromatics has been used to provide polypyrazolyl-substituted pyridine and pyrimidine ligands of potential value as lanthanide ion complexants. Ester substituents on the pyrazolyl groups can be reduced to the corresponding alcohol, which can in turn be converted to the bromide, then reacted with diethyl iminodiacetate to provide highly functionalized derivatives. Base hydrolysis converts these to polyanionic ligands, although the overall process is only efficient in the case of a pyridine core. The pyridine ligand with three pyrazolate and thus six carboxylate substituents forms stable, water-soluble Eu(III) and Tb(III) complexes displaying interesting spectroscopic properties with excited state lifetimes of about 1.6 ms and 1.0 ms, respectively, and quantum yields in the 4.5% to 13% range in water. Uncoordinated carboxylate groups in these complexes can be used for their grafting to polyacrylate polymer beads.
    DOI:
    10.1055/s-0032-1318219
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