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Acetic acid 7-acetoxy-2-{4-acetoxy-3-[4-(5,7-diacetoxy-4-oxo-4H-chromen-2-yl)-phenoxy]-phenyl}-4-oxo-4H-chromen-5-yl ester

中文名称
——
中文别名
——
英文名称
Acetic acid 7-acetoxy-2-{4-acetoxy-3-[4-(5,7-diacetoxy-4-oxo-4H-chromen-2-yl)-phenoxy]-phenyl}-4-oxo-4H-chromen-5-yl ester
英文别名
[4-(5,7-Diacetyloxy-4-oxochromen-2-yl)-2-[4-(5,7-diacetyloxy-4-oxochromen-2-yl)phenoxy]phenyl] acetate
Acetic acid 7-acetoxy-2-{4-acetoxy-3-[4-(5,7-diacetoxy-4-oxo-4H-chromen-2-yl)-phenoxy]-phenyl}-4-oxo-4H-chromen-5-yl ester化学式
CAS
——
化学式
C40H28O15
mdl
——
分子量
748.653
InChiKey
VVJUVTKKFPHBBP-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):
    4.7
  • 重原子数:
    55
  • 可旋转键数:
    14
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    193
  • 氢给体数:
    0
  • 氢受体数:
    15

反应信息

  • 作为产物:
    描述:
    Acetic acid 7-acetoxy-2-{4-acetoxy-3-[4-(5,7-diacetoxy-4-oxo-4H-chromen-2-yl)-phenoxy]-phenyl}-4-oxo-chroman-5-yl ester 在 potassium acetate 作用下, 以 溶剂黄146 为溶剂, 生成 Acetic acid 7-acetoxy-2-{4-acetoxy-3-[4-(5,7-diacetoxy-4-oxo-4H-chromen-2-yl)-phenoxy]-phenyl}-4-oxo-4H-chromen-5-yl ester
    参考文献:
    名称:
    Two New Biflavonoids from Ochna obtusata
    摘要:
    The leaves of Ochna obtusata (Ochnaceae) afforded two new biflavonoids together with the known compounds ochnaflavone, kaempferol 3-O-glucoside, and quercetin 3-O-glucoside. The new biflavonoids were characterized as 2,3-dihydroochnaflavone 7-O-methyl ether (1) and 2,3-dihydroochnaflavone (2) by spectral and chemical transformation studies.
    DOI:
    10.1021/np9604590
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文献信息

  • Two New Biflavonoids from <i>Ochna obtusata</i>
    作者:K. V. Rao、K. Sreeramulu、C. Venkata Rao、D. Gunasekar、M. T. Martin、B. Bodo
    DOI:10.1021/np9604590
    日期:1997.6.1
    The leaves of Ochna obtusata (Ochnaceae) afforded two new biflavonoids together with the known compounds ochnaflavone, kaempferol 3-O-glucoside, and quercetin 3-O-glucoside. The new biflavonoids were characterized as 2,3-dihydroochnaflavone 7-O-methyl ether (1) and 2,3-dihydroochnaflavone (2) by spectral and chemical transformation studies.
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