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3-(3',4'-dimethoxyphenyl)-6-hydroxy-4-methylcoumarin

中文名称
——
中文别名
——
英文名称
3-(3',4'-dimethoxyphenyl)-6-hydroxy-4-methylcoumarin
英文别名
3-(3,4-Dimethoxyphenyl)-6-hydroxy-4-methylchromen-2-one
3-(3',4'-dimethoxyphenyl)-6-hydroxy-4-methylcoumarin化学式
CAS
——
化学式
C18H16O5
mdl
MFCD02660671
分子量
312.322
InChiKey
XVUGUSLJPOBMDX-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):
    3
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    3-(3',4'-dimethoxyphenyl)-6-hydroxy-4-methylcoumarin1,4-二氧六环N,N-二甲基甲酰胺 为溶剂, 生成 3-(3,4-dimethoxyphenyl)-4,8,8-trimethyl-7,8,9,11-tetrahydropyrano[2,3-b]xanthene-2,10-dione
    参考文献:
    名称:
    逆电子需求Diels–Alder反应与3-芳基羟基香豆素的氨基甲基衍生物
    摘要:
    在逆电子需量Diels-Alder与烯胺的反应中,研究了由6和7-羟基香豆素衍生的Mannich碱的反应性。反应显示是通过环加成机理进行的,随后是半胱氨酸的转化,导致杂环吡喃并[2,3- a ]蒽,吡喃并[2,3- b ]并蒽和吡喃并[3,2- b]的形成。 x吨。
    DOI:
    10.1007/s10593-016-1907-6
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文献信息

  • Compounds exhibiting efflux inhibitor activity and composition and uses thereof
    申请人:Wempe Fitzpatrick Michael
    公开号:US20070254859A1
    公开(公告)日:2007-11-01
    At least one compound chosen from compounds of Formula I: a pharmaceutically acceptable salt or ester thereof, a solvate thereof, a chelate thereof, a non-covalent complex thereof, a prodrug thereof, and mixtures of any of the foregoing, wherein: n is a number from 1 to 900, wherein the individual units may be the same or different; W is chosen from alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; each of R 2 , R 3 , R 4 and R 5 is independently chosen from —H, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; Z′ is chosen from —O—, —N—, —NO—, —NR 4 —, —S—, —SO— and —SO 2 —, wherein R 4 is defined as above; each of X, X′, Y and Z is independently chosen from —CR 4 R 5 —, —NH—, —NR 4 —, —NO—, —O—, —NOR 4 —, —S—, —SO—, —SO 2 —, wherein R 4 and R 5 are defined as above; R 1 is chosen from a tocopherol, a steroid and a flavonoid; and R 6 is chosen from any R 1 , alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl.
  • Inverse electron demand Diels–Alder reactions with aminomethyl derivatives of 3-arylhydroxycoumarins
    作者:Galyna P. Mrug、Kostyantyn M. Kondratyuk、Svitlana P. Bondarenko、Mykhaylo S. Frasinyuk
    DOI:10.1007/s10593-016-1907-6
    日期:2016.7
    The reactivity of Mannich bases derived from 6- and 7-hydroxycoumarins was studied in inverse electron demand Diels–Alder reactions with enamines. The reactions were shown to proceed by a cycloaddition mechanism followed by transformation of hemiaminals and resulted in the formation of heterocyclic pyrano[2,3-a]xanthene, pyrano[2,3-b]xanthene, and pyrano[3,2-b]xanthene.
    在逆电子需量Diels-Alder与烯胺的反应中,研究了由6和7-羟基香豆素衍生的Mannich碱的反应性。反应显示是通过环加成机理进行的,随后是半胱氨酸的转化,导致杂环吡喃并[2,3- a ]蒽,吡喃并[2,3- b ]并蒽和吡喃并[3,2- b]的形成。 x吨。
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