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25-benzyloxy-1,4,11,14,21,30-hexaoxa-<4>-(1,2)-benzeno-<4>-(1,2)-benzeno-<2>-(2,6)-pyridino-<2>-(1,2)-benzenophane | 171000-41-2

中文名称
——
中文别名
——
英文名称
25-benzyloxy-1,4,11,14,21,30-hexaoxa-<4>-(1,2)-benzeno-<4>-(1,2)-benzeno-<2>-(2,6)-pyridino-<2>-(1,2)-benzenophane
英文别名
——
25-benzyloxy-1,4,11,14,21,30-hexaoxa-<4>-(1,2)-benzeno-<4>-(1,2)-benzeno-<2>-(2,6)-pyridino-<2>-(1,2)-benzenophane化学式
CAS
171000-41-2
化学式
C36H33NO7
mdl
——
分子量
591.661
InChiKey
JHUDGQXBEDVVSZ-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):
    7.05
  • 重原子数:
    44.0
  • 可旋转键数:
    3.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    77.5
  • 氢给体数:
    0.0
  • 氢受体数:
    8.0

反应信息

  • 作为反应物:
    描述:
    25-benzyloxy-1,4,11,14,21,30-hexaoxa-<4>-(1,2)-benzeno-<4>-(1,2)-benzeno-<2>-(2,6)-pyridino-<2>-(1,2)-benzenophane 在 palladium on activated charcoal 氢气 作用下, 以 乙酸乙酯 为溶剂, 25.0 ℃ 、303.97 kPa 条件下, 反应 4.0h, 以73%的产率得到1,4,11,14,21,30-hexaoxa-<4>-(1,2)-benzeno-<4>-(1,2)-benzeno-<2>-(2,6)-4-pyridino-<2>-(1,2)-benzenophane
    参考文献:
    名称:
    Benzo condensed crown ethers containing 1,8-naphthyridine or 4-pyridone units - synthesis and complex formation with organic guest molecules
    摘要:
    New crown compounds 3-5 comprising beside o-phenylene groups 1,8-naphthyridine or 4-pyridone groups as characteristic building units are synthesized. They form numerous stoichiometric crystalline complexes with uncharged organic molecules including alcohols, nitro compounds and other dipolar-aprotic solvents, as well as cyclic ethers and aromatic hydrocarbons. Properties of complex formation and host-guest stoichiometries are discussed making a comparison with parent host analogues.
    DOI:
    10.1002/prac.19953370198
  • 作为产物:
    参考文献:
    名称:
    Benzo condensed crown ethers containing 1,8-naphthyridine or 4-pyridone units - synthesis and complex formation with organic guest molecules
    摘要:
    New crown compounds 3-5 comprising beside o-phenylene groups 1,8-naphthyridine or 4-pyridone groups as characteristic building units are synthesized. They form numerous stoichiometric crystalline complexes with uncharged organic molecules including alcohols, nitro compounds and other dipolar-aprotic solvents, as well as cyclic ethers and aromatic hydrocarbons. Properties of complex formation and host-guest stoichiometries are discussed making a comparison with parent host analogues.
    DOI:
    10.1002/prac.19953370198
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