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4'-苄氧基-5-羟基-3-甲氧基-7-(甲氧基甲氧基)黄酮 | 943827-54-1

中文名称
4'-苄氧基-5-羟基-3-甲氧基-7-(甲氧基甲氧基)黄酮
中文别名
——
英文名称
4'-benzyloxy-5-hydroxy-3-methoxy-7-(methoxymethyloxy)flavone
英文别名
5-Hydroxy-3-methoxy-7-(methoxymethoxy)-2-(4-phenylmethoxyphenyl)chromen-4-one
4'-苄氧基-5-羟基-3-甲氧基-7-(甲氧基甲氧基)黄酮化学式
CAS
943827-54-1
化学式
C25H22O7
mdl
——
分子量
434.445
InChiKey
VOUOJMNGALCLCW-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

物化性质

  • 沸点:
    653.6±55.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    32
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    83.4
  • 氢给体数:
    1
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4'-苄氧基-5-羟基-3-甲氧基-7-(甲氧基甲氧基)黄酮 在 palladium on activated charcoal aluminum tri-bromide 、 4 A molecular sieve 、 氢气potassium carbonatesilver(l) oxide 作用下, 以 二氯甲烷乙酸乙酯乙腈 为溶剂, 反应 55.0h, 生成 [(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxychromen-7-yl]oxy-2-methyloxan-3-yl] acetate
    参考文献:
    名称:
    Synthesis of Kaempferitrin
    摘要:
    A short synthesis of Kaempferitrin (1), a 3,7-diglycosylflavone, is reported. Key features include the synthesis of a protected form of kaempferol in which all four hydroxy groups are differentiated and the first bis-glycosylation of a dihydroxyflavone. This synthesis will allow the preparation of derivatives for further explorations into the origins of this compound's biological activity.
    DOI:
    10.1021/jo070502w
  • 作为产物:
    参考文献:
    名称:
    Synthesis of Kaempferitrin
    摘要:
    A short synthesis of Kaempferitrin (1), a 3,7-diglycosylflavone, is reported. Key features include the synthesis of a protected form of kaempferol in which all four hydroxy groups are differentiated and the first bis-glycosylation of a dihydroxyflavone. This synthesis will allow the preparation of derivatives for further explorations into the origins of this compound's biological activity.
    DOI:
    10.1021/jo070502w
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文献信息

  • Synthesis of Kaempferitrin
    作者:Sameer Urgaonkar、Jared T. Shaw
    DOI:10.1021/jo070502w
    日期:2007.6.1
    A short synthesis of Kaempferitrin (1), a 3,7-diglycosylflavone, is reported. Key features include the synthesis of a protected form of kaempferol in which all four hydroxy groups are differentiated and the first bis-glycosylation of a dihydroxyflavone. This synthesis will allow the preparation of derivatives for further explorations into the origins of this compound's biological activity.
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