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6-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,4-dihydro-1H-1,4-diazepinium perchlorate | 1354972-96-5

中文名称
——
中文别名
——
英文名称
6-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,4-dihydro-1H-1,4-diazepinium perchlorate
英文别名
6-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1H-1,4-diazepin-4-ium;perchlorate
6-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,4-dihydro-1H-1,4-diazepinium perchlorate化学式
CAS
1354972-96-5
化学式
C14H18N2O3*ClHO4
mdl
——
分子量
362.767
InChiKey
QYGKWRGHTIMJRY-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):
    -4.95
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    128
  • 氢给体数:
    2
  • 氢受体数:
    8

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis and Characterization of New Derivatives of 1,4-Diazepinium Salts
    摘要:
    Novel 6-aryl-1,4-diazepinium and 3-aryl-hexahydro-1H-benzo-[b-1,4]diazepinium salts (with aryl and heteroaryl=1-quinilinio, 3,5-dimethylpyridinio, 4-phenyl phenyl, 3,4,5-trimethoxyphenyl, and 1,4-phenylene) were synthesized mostly by reactions of 1,2-diamines with 3-aryl and 3-heteroaryl-1,5-diazapentadienium salts. The ultraviolet spectral behavior of these compounds was examined in acetonitrile. Elemental analysis, infrared, H-1 NMR, C-13 NMR, and mass spectra confirmed the molecular structure of the newly synthesized compounds.
    DOI:
    10.1080/00397911.2010.518332
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文献信息

  • Synthesis and Characterization of New Derivatives of 1,4-Diazepinium Salts
    作者:A. M. Mehranpour、S. Hashemnia、Z. Shayan
    DOI:10.1080/00397911.2010.518332
    日期:2011.12.1
    Novel 6-aryl-1,4-diazepinium and 3-aryl-hexahydro-1H-benzo-[b-1,4]diazepinium salts (with aryl and heteroaryl=1-quinilinio, 3,5-dimethylpyridinio, 4-phenyl phenyl, 3,4,5-trimethoxyphenyl, and 1,4-phenylene) were synthesized mostly by reactions of 1,2-diamines with 3-aryl and 3-heteroaryl-1,5-diazapentadienium salts. The ultraviolet spectral behavior of these compounds was examined in acetonitrile. Elemental analysis, infrared, H-1 NMR, C-13 NMR, and mass spectra confirmed the molecular structure of the newly synthesized compounds.
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