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2-hydroxy-3',5'-dinitroflavanone | 953129-47-0

中文名称
——
中文别名
——
英文名称
2-hydroxy-3',5'-dinitroflavanone
英文别名
——
2-hydroxy-3',5'-dinitroflavanone化学式
CAS
953129-47-0
化学式
C15H10N2O7
mdl
——
分子量
330.254
InChiKey
UWNLEQKYCVASQK-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):
    2.31
  • 重原子数:
    24.0
  • 可旋转键数:
    3.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    132.81
  • 氢给体数:
    1.0
  • 氢受体数:
    7.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-hydroxy-3',5'-dinitroflavanone对甲苯磺酸 作用下, 以 二甲基亚砜 为溶剂, 以59%的产率得到3',5'-dinitro-Flavone
    参考文献:
    名称:
    Efficient Synthesis of Nitroflavones by Cyclodehydrogenation of 2′-Hydroxychalcones and by the Baker-Venkataraman Method
    摘要:
    Several nitroflavone derivatives were synthesized by cyclodehydrogenation of 2'-hydroxychalcones and by the Baker-Venkataraman approach, starting from 2'-hydroxyacetophenones and benzoic acid derivatives. Nitroflavones synthesised by the first synthetic approach were obtained in better global yields than those obtained by the later method. The structures of all new compounds were elucidated by microanalyses, 1D and 2D NMR, IR, and mass spectroscopic measurements.
    DOI:
    10.1007/s00706-006-0550-9
  • 作为产物:
    描述:
    2'-羟基苯乙酮 在 sodium hydride 作用下, 以 四氢呋喃吡啶 为溶剂, 反应 6.5h, 生成 2-hydroxy-3',5'-dinitroflavanone
    参考文献:
    名称:
    Efficient Synthesis of Nitroflavones by Cyclodehydrogenation of 2′-Hydroxychalcones and by the Baker-Venkataraman Method
    摘要:
    Several nitroflavone derivatives were synthesized by cyclodehydrogenation of 2'-hydroxychalcones and by the Baker-Venkataraman approach, starting from 2'-hydroxyacetophenones and benzoic acid derivatives. Nitroflavones synthesised by the first synthetic approach were obtained in better global yields than those obtained by the later method. The structures of all new compounds were elucidated by microanalyses, 1D and 2D NMR, IR, and mass spectroscopic measurements.
    DOI:
    10.1007/s00706-006-0550-9
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