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(2R,3R,4S)-4-(2-amino-4,6-dimethoxyphenyl)-2-(3,4-dihydroxyphenyl)chroman-3,5,7-triol | 1169702-46-8

中文名称
——
中文别名
——
英文名称
(2R,3R,4S)-4-(2-amino-4,6-dimethoxyphenyl)-2-(3,4-dihydroxyphenyl)chroman-3,5,7-triol
英文别名
(2R,3R,4S)-4-(2-amino-4,6-dimethoxyphenyl)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol
(2R,3R,4S)-4-(2-amino-4,6-dimethoxyphenyl)-2-(3,4-dihydroxyphenyl)chroman-3,5,7-triol化学式
CAS
1169702-46-8
化学式
C23H23NO8
mdl
——
分子量
441.438
InChiKey
IUFKNQDYFQPJIT-YTFSRNRJSA-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):
    2.1
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    155
  • 氢给体数:
    6
  • 氢受体数:
    9

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

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文献信息

  • Sustainability from agricultural waste: chiral ligands from oligomeric proanthocyanidins via acid-mediated depolymerization
    作者:Caili Fu、Wei Chen、Yi Ling Quek、Runyan Ni、Amylia Bte Abdul Ghani、Wendy Wen Yi Leong、Huaqiang Zeng、Dejian Huang
    DOI:10.1016/j.tetlet.2010.09.123
    日期:2010.12
    Oligomeric proanthocyanidins (OPCs, Ar' = 3,4-(HO)(2)(C6H3) are abundant natural products found in agricultural and forestry waste such as pine bark, grape seeds, and the peels of mangosteen. We have demonstrated that the OPCs can be converted into small molecule chiral ligands by using proper nucleophiles for acid depolymerization of the OPCs. The chiral ligands may have potential for sustainable asymmetric catalysis. (C) 2010 Elsevier Ltd. All rights reserved.
  • METHOD OF PREPARING DERIVATIVES/OLIGOMERS OF EPICATECHIN AND APPLICATIONS THEREOF
    申请人:Huang Dejian
    公开号:US20120323016A1
    公开(公告)日:2012-12-20
    The present invention relates to the preparation of a class of novel, optically active compounds derived from oligomeric proanthocyanidins (OPCs), more particularly to oligomers of epicatechin. These compounds include multidentate ligands and their metal complexes for use in catalysis. Methods of depolymerising proanthocyanidins to form catechins, and particularly depolymerising proanthocyanidins derived from plant sources to form novel epicatechins having application in catalysis are disclosed.
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