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2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-1,3-benzoxazine | 312527-47-2

中文名称
——
中文别名
——
英文名称
2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-1,3-benzoxazine
英文别名
2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-3,1-benzoxazine;2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,2-dihydro-4H-3,1-benzoxazine;2-(4,4-diphenyl-1,4-dihydro-2H-3,1-benzoxazin-2-yl)-4-nitrophenol;2-(4,4-diphenyl-1,2-dihydro-3,1-benzoxazin-2-yl)-4-nitrophenol
2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-1,3-benzoxazine化学式
CAS
312527-47-2
化学式
C26H20N2O4
mdl
——
分子量
424.456
InChiKey
HECOOGIMGIPIGR-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

物化性质

  • 熔点:
    155-158 °C
  • 沸点:
    580.5±50.0 °C(Predicted)
  • 密度:
    1.307±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.6
  • 重原子数:
    32
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    87.3
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 下游产品
    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-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-1,3-benzoxazine聚合甲醛溶剂黄146 为溶剂, 以65%的产率得到10-nitro-13,13-diphenyl-11bH,13H-[3,1]benzoxazino[1,2-c][1,3]benzoxazine
    参考文献:
    名称:
    Studies of 4H-3,1-benzoxazines. 14. Structure and some properties of 2-[2-hydroxyphenyl(naphthyl)]-1,2-dihydro-4H-3,1-benzoxazines
    摘要:
    DOI:
    10.1007/s10593-006-0205-0
  • 作为产物:
    描述:
    (2-aminophenyl)diphenylmethanol5-硝基水杨醛溶剂黄146 为溶剂, 以72%的产率得到2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-1,3-benzoxazine
    参考文献:
    名称:
    Studies of 4H-3,1-benzoxazines. 14. Structure and some properties of 2-[2-hydroxyphenyl(naphthyl)]-1,2-dihydro-4H-3,1-benzoxazines
    摘要:
    DOI:
    10.1007/s10593-006-0205-0
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文献信息

  • Synthesis and study of copper(II), nickel(II), and cobalt(II) complex compounds with dihydrobenzoxazine derivatives
    作者:T. E. Apenysheva、K. S. Pushkareva、S. N. Bolotin、V. Yu. Frolov、F. A. Kolokolov、E. V. Gromachevskaya、A. A. Borodavko、T. P. Kosulina
    DOI:10.1134/s1070363206040244
    日期:2006.4
    Complex compounds ML2 of copper(II), nickel(II), and cobalt(II) with 2-(2-hydroxy-5-nitrophenyl)-4,4-diphenyl-1,4-dihydro-2H-3,1-benzoxazine and 2-(2-hydroxyphenyl)-4,4-diphenyl-1,4-dihydro-2H-3,1-benzoxazine (HL) were prepared by electrochemical and chemical syntheses. The complex formation involves the azomethine form of the ligand and gives a six-membered chelate cycle comprising deprotonated phenol and azomethine groups. The coordination entity has a planar structure with trans arrangement of the nitrogen and oxygen atoms.
  • Synthesis of copper(II) coordination compounds with benzoxazine derivatives
    作者:A. I. Oflidi、T. E. Apenysheva、K. S. Pushkaryova、V. Yu. Frolov、S. N. Bolotin、F. A. Kolokolov、V. T. Panyushkin
    DOI:10.1134/s0036023609010136
    日期:2009.1
    Copper(II) complexes with 1,2-dihydro-4H-3,1-benzoxazine(HL) derivatives, CuLOH, were prepared by anodic electrosynthesis. The use of an amalgamated copper anode resulted in an increase in the electrosynthesis rate. It follows from the IR spectra of the products that the benzoxazine ring in the ligand molecule is opened upon complexation, while a six-membered chelate ring involving the oxygen atom of the deprotonated phenol group and the imine nitrogen atom is formed.
  • Studies of 4H-3,1-benzoxazines. 14. Structure and some properties of 2-[2-hydroxyphenyl(naphthyl)]-1,2-dihydro-4H-3,1-benzoxazines
    作者:E. V. Gromachevskaya、T. P. Kosulina、A. A. Borodavko
    DOI:10.1007/s10593-006-0205-0
    日期:2006.8
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