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1,1'-(1,3-phenylene)bis[2-(5-methyl-2-nitrophenyl)ethanol] | 1227098-14-7

中文名称
——
中文别名
——
英文名称
1,1'-(1,3-phenylene)bis[2-(5-methyl-2-nitrophenyl)ethanol]
英文别名
1-[3-[1-Hydroxy-2-(5-methyl-2-nitrophenyl)ethyl]phenyl]-2-(5-methyl-2-nitrophenyl)ethanol;1-[3-[1-hydroxy-2-(5-methyl-2-nitrophenyl)ethyl]phenyl]-2-(5-methyl-2-nitrophenyl)ethanol
1,1'-(1,3-phenylene)bis[2-(5-methyl-2-nitrophenyl)ethanol]化学式
CAS
1227098-14-7
化学式
C24H24N2O6
mdl
——
分子量
436.464
InChiKey
OHXKBAIBQSNDRG-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):
    4.5
  • 重原子数:
    32
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    132
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    间苯二甲醛5-甲基-2-硝基苄氯四(二甲氨基)乙烯 、 sodium iodide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 26.0h, 以54%的产率得到1,1'-(1,3-phenylene)bis[2-(5-methyl-2-nitrophenyl)ethanol]
    参考文献:
    名称:
    First TDAE-Mediated Double Addition of Nitrobenzylic Anions to Aromatic Dialdehydes
    摘要:
    We report herein the first tetrakis(dimethylamino) ethylene (TDAE)-mediated double addition of nitrobenzylic anions to aromatic dialdehydes such as terephthalaldehyde and isophthalaldehyde, and have developed a new methodology that allows us to observe the double addition. This TDAE-mediated approach is an original and mild method with which to generate tri-aromatic diols.
    DOI:
    10.1055/s-0029-1218590
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文献信息

  • First TDAE-Mediated Double Addition of Nitrobenzylic Anions to Aromatic Dialdehydes
    作者:Patrice Vanelle、Thierry Juspin、Gamal Giuglio-Tonolo、Thierry Terme
    DOI:10.1055/s-0029-1218590
    日期:2010.3
    We report herein the first tetrakis(dimethylamino) ethylene (TDAE)-mediated double addition of nitrobenzylic anions to aromatic dialdehydes such as terephthalaldehyde and isophthalaldehyde, and have developed a new methodology that allows us to observe the double addition. This TDAE-mediated approach is an original and mild method with which to generate tri-aromatic diols.
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