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3-(2-(4-methoxybenzyl)-4-oxo-4H-chromen-3-yl)-4-(4-methoxyphenyl)-1-methyl-9H-xanthen-9-one | 1233534-06-9

中文名称
——
中文别名
——
英文名称
3-(2-(4-methoxybenzyl)-4-oxo-4H-chromen-3-yl)-4-(4-methoxyphenyl)-1-methyl-9H-xanthen-9-one
英文别名
4-(4-Methoxyphenyl)-3-[2-[(4-methoxyphenyl)methyl]-4-oxochromen-3-yl]-1-methylxanthen-9-one;4-(4-methoxyphenyl)-3-[2-[(4-methoxyphenyl)methyl]-4-oxochromen-3-yl]-1-methylxanthen-9-one
3-(2-(4-methoxybenzyl)-4-oxo-4H-chromen-3-yl)-4-(4-methoxyphenyl)-1-methyl-9H-xanthen-9-one化学式
CAS
1233534-06-9
化学式
C38H28O6
mdl
——
分子量
580.637
InChiKey
LUOYRSVMOJBZHV-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):
    8.1
  • 重原子数:
    44
  • 可旋转键数:
    6
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    71.1
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    3-[2-(4-methoxyphenyl)ethynyl]-2-methyl-4H-chromen-4-one 在 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 二甲基亚砜 为溶剂, 反应 0.17h, 以85%的产率得到3-(2-(4-methoxybenzyl)-4-oxo-4H-chromen-3-yl)-4-(4-methoxyphenyl)-1-methyl-9H-xanthen-9-one
    参考文献:
    名称:
    Efficient Construction of a 3C-Xanthone-Linked 3C-Chromone Scaffold by Novel Double Michael Additions and Cyclizations
    摘要:
    A novel base-promoted cascade reaction of 2-methyl-3-(1-alkynyl)chromones to produce a 3C-xanthone-linked 3C-chromone scaffold has been developed. This tandem process involves multiple reactions such as Michael additions/cyclizations under mild conditions without a transition metal catalyst and inert atmosphere.
    DOI:
    10.1021/ol101100d
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文献信息

  • Efficient Construction of a 3<i>C</i>-Xanthone-Linked 3<i>C</i>-Chromone Scaffold by Novel Double Michael Additions and Cyclizations
    作者:Fuchun Xie、Hong Chen、Youhong Hu
    DOI:10.1021/ol101100d
    日期:2010.7.2
    A novel base-promoted cascade reaction of 2-methyl-3-(1-alkynyl)chromones to produce a 3C-xanthone-linked 3C-chromone scaffold has been developed. This tandem process involves multiple reactions such as Michael additions/cyclizations under mild conditions without a transition metal catalyst and inert atmosphere.
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