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7-allyl-8-hydroxycoumarin | 91368-56-8

中文名称
——
中文别名
——
英文名称
7-allyl-8-hydroxycoumarin
英文别名
8-Hydroxy-7-allyl-cumarin;7-allyl-8-hydroxy-2H-chromen-2-one;7-allyl-8-hydroxy-chromen-2-one;8-Hydroxy-7-prop-2-enylchromen-2-one
7-allyl-8-hydroxycoumarin化学式
CAS
91368-56-8
化学式
C12H10O3
mdl
——
分子量
202.21
InChiKey
SSQLKBYAGIZWFJ-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

  • 熔点:
    158.6-159.5 °C(Solv: ethanol (64-17-5))
  • 沸点:
    372.8±42.0 °C(Predicted)
  • 密度:
    1.264±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 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
  • 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:
    参考文献:
    名称:
    Guiotto, A.; Manzini, P.; Chilin, A., Journal of Heterocyclic Chemistry, 1985, vol. 22, p. 649 - 656
    摘要:
    DOI:
  • 作为产物:
    描述:
    8-羟基苯并吡喃-2-酮potassium carbonate 作用下, 以 乙二醇丙酮 为溶剂, 反应 22.0h, 生成 7-allyl-8-hydroxycoumarin
    参考文献:
    名称:
    Synthesis and biological evaluation of fused oxepinocoumarins as free radicals scavengers
    摘要:
    Some fused dihydrooxepino[f]-, [g]-, and [h]coumarins were obtained from the ring-closing metathesis of the corresponding o-allyl-allyloxycoumarins under the treatment with the first generation Grubbs' catalyst. These compounds were tested in vitro for their antioxidant activity, and they present significant scavenging activity. They were also showed to inhibit in vitro soybean lipoxygenase.
    DOI:
    10.3109/14756366.2011.555944
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文献信息

  • Synthesis and biological evaluation of fused oxepinocoumarins as free radicals scavengers
    作者:Konstantinos E. Litinas、Alexandros Mangos、Thomas E. Nikkou、Dimitra J. Hadjipavlou-Litina
    DOI:10.3109/14756366.2011.555944
    日期:2011.12.1
    Some fused dihydrooxepino[f]-, [g]-, and [h]coumarins were obtained from the ring-closing metathesis of the corresponding o-allyl-allyloxycoumarins under the treatment with the first generation Grubbs' catalyst. These compounds were tested in vitro for their antioxidant activity, and they present significant scavenging activity. They were also showed to inhibit in vitro soybean lipoxygenase.
  • Guiotto, A.; Manzini, P.; Chilin, A., Journal of Heterocyclic Chemistry, 1985, vol. 22, p. 649 - 656
    作者:Guiotto, A.、Manzini, P.、Chilin, A.、Pastorini, G.、Rodighiero, P.
    DOI:——
    日期:——
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