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Piscerygenin | 67978-85-2

中文名称
——
中文别名
——
英文名称
Piscerygenin
英文别名
5,7,2',4'-Tetrahydroxy-5'-methoxy-isoflavon;3-(2,4-dihydroxy-5-methoxy-phenyl)-5,7-dihydroxy-chromen-4-one;3-(2,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxychromen-4-one
Piscerygenin化学式
CAS
67978-85-2
化学式
C16H12O7
mdl
——
分子量
316.267
InChiKey
OEWYVOHIQUVAAO-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):
    2.3
  • 重原子数:
    23
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    116
  • 氢给体数:
    4
  • 氢受体数:
    7

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:
    描述:
    Piscerygenin邻四氯苯醌 作用下, 以 1,4-二氧六环 为溶剂, 反应 2.0h, 以49%的产率得到desmoxyphyllin A
    参考文献:
    名称:
    Facile synthesis of polyhydroxycoumaronochromones with quinones: synthesis of alkylpolyhydroxy- and alkoxycoumaronochromones from 2′-hydroxyisoflavones
    摘要:
    4 ' ,5,7-Trihydroxy- or 8-alkyl-4 ' .5,7-trihvclroxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2 ' -hydroxyisoflavones with o-chloranil under mild conditions. By contrast, alkoxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2 ' -hydroxyisoflavones with DDQ. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)01234-5
  • 作为产物:
    描述:
    Acetic acid 3,5-bis-benzyloxy-2-[2-(2,4-bis-benzyloxy-5-methoxy-phenyl)-3,3-dimethoxy-propionyl]-phenyl ester 在 palladium on activated charcoal sodium hydroxide氢气 作用下, 以 四氢呋喃1,4-二氧六环甲醇 为溶剂, 反应 10.0h, 生成 Piscerygenin
    参考文献:
    名称:
    Facile synthesis of polyhydroxycoumaronochromones with quinones: synthesis of alkylpolyhydroxy- and alkoxycoumaronochromones from 2′-hydroxyisoflavones
    摘要:
    4 ' ,5,7-Trihydroxy- or 8-alkyl-4 ' .5,7-trihvclroxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2 ' -hydroxyisoflavones with o-chloranil under mild conditions. By contrast, alkoxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2 ' -hydroxyisoflavones with DDQ. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(01)01234-5
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文献信息

  • Facile synthesis of polyhydroxycoumaronochromones with quinones: synthesis of alkylpolyhydroxy- and alkoxycoumaronochromones from 2′-hydroxyisoflavones
    作者:Masao Tsukayama、Akihiro Oda、Yasuhiko Kawamura、Masaki Nishiuchi、Kazuyo Yamashita
    DOI:10.1016/s0040-4039(01)01234-5
    日期:2001.8
    4 ' ,5,7-Trihydroxy- or 8-alkyl-4 ' .5,7-trihvclroxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2 ' -hydroxyisoflavones with o-chloranil under mild conditions. By contrast, alkoxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2 ' -hydroxyisoflavones with DDQ. (C) 2001 Elsevier Science Ltd. All rights reserved.
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