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8,17-Dioxa-1,10-diazapentacyclo[11.5.3.34,10.016,20.07,23]tetracosa-4(24),5,7(23),13(21),14,16(20)-hexaene | 1130299-93-2

中文名称
——
中文别名
——
英文名称
8,17-Dioxa-1,10-diazapentacyclo[11.5.3.34,10.016,20.07,23]tetracosa-4(24),5,7(23),13(21),14,16(20)-hexaene
英文别名
8,17-dioxa-1,10-diazapentacyclo[11.5.3.34,10.016,20.07,23]tetracosa-4(24),5,7(23),13(21),14,16(20)-hexaene
8,17-Dioxa-1,10-diazapentacyclo[11.5.3.34,10.016,20.07,23]tetracosa-4(24),5,7(23),13(21),14,16(20)-hexaene化学式
CAS
1130299-93-2
化学式
C20H22N2O2
mdl
——
分子量
322.407
InChiKey
DQFQPBWKKHIWQK-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):
    3.3
  • 重原子数:
    24
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    24.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • One-step synthesis of a new heterocyclophane family
    作者:Rodolfo Quevedo、Bárbara Moreno-Murillo
    DOI:10.1016/j.tetlet.2008.12.023
    日期:2009.2
    New macrocyclic compounds having two benzoxazine subunits joined by two ethylene bridges have been prepared by Mannich condensation of the appropriate 4-hydi-oxyphenylethylamine with an excess of formaldehyde. This is a general method for synthesising a new family of heterocyclophanes. (C) 2008 Elsevier Ltd. All rights reserved.
  • Intrinsic Fluorescence of 1,3-Benzoxazinephanes
    作者:Rodolfo Quevedo、Cesar A. Sierra
    DOI:10.3987/com-11-12324
    日期:——
    A new 1,3-benzoxazine nuclei-based fluorescent system is presented. The photophysical aspects are briefly discussed. The results suggested that the presence of oxazinic methylenes is necessary for fluorescence to be present.
  • A structural study of the intermolecular interactions of tyramine in the solid state and in solution
    作者:Rodolfo Quevedo、Nelson Nuñez-Dallos、Klaus Wurst、Álvaro Duarte-Ruiz
    DOI:10.1016/j.molstruc.2012.07.013
    日期:2012.12
    The nature of the interactions between tyramine units was investigated in the solid state and in solution. Crystals of tyramine in its free base form were analyzed by Fourier transform infrared (FT-IR) spectroscopy and single-crystal X-ray diffraction (XRD). The crystal structure shows a linear molecular organization held together by "head-to-tail" intermolecular hydrogen bonds between the amino groups and the phenolic hydroxyl groups. These chains are arranged in double layers that can geometrically favor the formation of templates in solution, which may facilitate macrocyclization reactions to form azacyclophane-type compounds. Computational calculations using the PM6-DH+ method and electrospray ionization mass spectrometry (ESI-HRMS) reveal that the formation of a hydrogen-bonded tyramine dimer is favored in solution. (C) 2012 Elsevier B.V. All rights reserved.
  • 1H- and 13C-NMR spectroscopic study of intermolecular interactions between tyrosine-derived azacyclophanes and aromatic rings
    作者:Rodolfo Quevedo
    DOI:10.1016/j.molstruc.2020.127777
    日期:2020.5
    Abstract This article analyses intermolecular interactions in solution between l -tyrosine-derived pentacyclic azacyclophanes and some aromatic compounds (p-tert-butylphenol, 2-tert-butyl-4-methoxyphenol and benzene). The results showed that these azacyclophanes formed complexes with aromatic compounds, in a 1:1 ratio, by means of pi-stacking.
    摘要 本文分析了l-酪氨酸衍生的五环氮杂环芳烃与一些芳香族化合物(对叔丁基苯酚、2-叔丁基-4-甲氧基苯酚和苯)在溶液中的分子间相互作用。结果表明,这些氮杂环芳烃通过π-堆积与芳香族化合物以1:1的比例形成复合物。
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