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7-(2-methylphenoxy)-4-methylcoumarin | 1413441-46-9

中文名称
——
中文别名
——
英文名称
7-(2-methylphenoxy)-4-methylcoumarin
英文别名
4-Methyl-7-(2-methylphenoxy)chromen-2-one;4-methyl-7-(2-methylphenoxy)chromen-2-one
7-(2-methylphenoxy)-4-methylcoumarin化学式
CAS
1413441-46-9
化学式
C17H14O3
mdl
——
分子量
266.296
InChiKey
CENONNHRUKSHAA-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):
    4.1
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 作为产物:
    描述:
    羟甲香豆素2-甲基苯硼酸 在 copper diacetate 、 三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以54%的产率得到7-(2-methylphenoxy)-4-methylcoumarin
    参考文献:
    名称:
    Expedient Synthesis of Biologically Potent Aryloxycoumarins and (Aryloxyimino)ethylcoumarins via Copper(II)-Promoted Chan–Lam Coupling Reaction
    摘要:
    A convenient protocol for the efficient synthesis of aryloxycoumarins and (aryloxyimino) ethylcoumarins is described. The synthetic route developed involves the Cu-promoted C-O and N-O coupling reactions from readily available hydroxycoumarin and (hydroxyimino)ethylcoumarin derivatives in the presence of the catalytic system Cu(OAc)(2)/Et3N. By applying this condition, a series of arylboronic acids have been successfully reacted to afford the coupled products in fair to good yields.
    DOI:
    10.1080/00397911.2011.594544
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文献信息

  • Expedient Synthesis of Biologically Potent Aryloxycoumarins and (Aryloxyimino)ethylcoumarins via Copper(II)-Promoted Chan–Lam Coupling Reaction
    作者:Arunima Medda、Gargi Pal、Raghunath Singha、Tabassum Hossain、Achintya Saha、Asish R. Das
    DOI:10.1080/00397911.2011.594544
    日期:2013.1
    A convenient protocol for the efficient synthesis of aryloxycoumarins and (aryloxyimino) ethylcoumarins is described. The synthetic route developed involves the Cu-promoted C-O and N-O coupling reactions from readily available hydroxycoumarin and (hydroxyimino)ethylcoumarin derivatives in the presence of the catalytic system Cu(OAc)(2)/Et3N. By applying this condition, a series of arylboronic acids have been successfully reacted to afford the coupled products in fair to good yields.
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