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2-(4-decyloxyphenyl)-4-hydroxy-3-oxo-3,4-dihydroquinoxalin-1-oxide | 488853-25-4

中文名称
——
中文别名
——
英文名称
2-(4-decyloxyphenyl)-4-hydroxy-3-oxo-3,4-dihydroquinoxalin-1-oxide
英文别名
3-(4-decoxyphenyl)-1-hydroxy-4-oxidoquinoxalin-4-ium-2-one
2-(4-decyloxyphenyl)-4-hydroxy-3-oxo-3,4-dihydroquinoxalin-1-oxide化学式
CAS
488853-25-4
化学式
C24H30N2O4
mdl
——
分子量
410.513
InChiKey
QBOIBZYNPGORBO-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):
    5.3
  • 重原子数:
    30
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    78.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    N-(2-nitrosophenyl)hydroxylamine4-decyloxyphenylglyoxal乙醇 为溶剂, 反应 0.5h, 以40%的产率得到2-(4-decyloxyphenyl)-4-hydroxy-3-oxo-3,4-dihydroquinoxalin-1-oxide
    参考文献:
    名称:
    Langmuir-blodgett films of hydroxamic acid of the quinoxalinone series
    摘要:
    Amphiphilic hydroxamic acid 2-(4-decyloxyphenyl)-4-hydroxy-3-oxo-3,4-dihydroquinoxalin-1-oxide was synthesized. The conditions of the formation of hydroxamic acid and its lead, europium, cadmium, and copper salt monomolecular layers were studied. Multimolecular systems were prepared by the Langmuir Blodgett method from various solvents, including chloroform, carbon tetrachloride, and toluene. The films were characterized by small angle X-ray scattering, UV and IR spectroscopy, ellipsometry, and atomic-force microscopy. The UV data and monolayer compression isotherms showed changes in the state of hydroxamic acid in various solvents in the presence of light and in the dark. The suggestion was made that changes in solutions were related to aggregation phenomenon.
    DOI:
    10.1134/s0036024409040232
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