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(2R,3R)-2-bromo-3-hydroxy-3-phenylpropanoic acid | 130853-41-7

中文名称
——
中文别名
——
英文名称
(2R,3R)-2-bromo-3-hydroxy-3-phenylpropanoic acid
英文别名
——
(2R,3R)-2-bromo-3-hydroxy-3-phenylpropanoic acid化学式
CAS
130853-41-7
化学式
C9H9BrO3
mdl
——
分子量
245.073
InChiKey
PNZTVDQYHQRHKB-HTQZYQBOSA-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):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    57.5
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • Stereoselective chemoenzymatic process for the preparation of optically enriched phenylglycidates as precursors of taxol side chain
    申请人:COUNCIL OF SCIENTIFIC AND INDUSTRIAL
    公开号:US20040259943A1
    公开(公告)日:2004-12-23
    The present invention relates to a novel and efficient chemoenzymatic process of preparation of optically active trans alkyl phenylglycidates. The invention particularly discloses a novel process for the chemoenzymatic synthesis of two enantiomers of trans alkyl phenylglycidate i.e. alkyl(2S,3R)-phenylglycidate and alkyl(2R,3S)-phenylglycidate of formulae 7 and 8 respectively. 1
    本发明涉及一种新颖有效的化学酶法制备光学活性反式烷基苯基乙二酸酯的方法。该发明特别揭示了一种新的化学酶法合成反式烷基苯基乙二酸酯的两个对映异构体,即式7和式8的烷基(2S,3R)-苯基乙二酸酯和烷基(2R,3S)-苯基乙二酸酯。
  • STEREOSELECTIVE CHEMOENZYMATIC PROCESS FOR PREPARING OPTICALLY ENRICHED PHENYLGLYCIDATES
    申请人:COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH
    公开号:EP1601778A1
    公开(公告)日:2005-12-07
  • [EN] STEREOSELECTIVE CHEMOENZYMATIC PROCESS FOR PREPARING OPTICALLY ENRICHED PHENYLGLYCIDATES<br/>[FR] PROCEDE CHIMIOENZYMATIQUE STEREOSELECTIF POUR LA PREPARATION DE PHENYLGLYCIDATES OPTIQUEMENT ENRICHIS
    申请人:COUNCIL SCIENT IND RES
    公开号:WO2004081219A1
    公开(公告)日:2004-09-23
    The present invention relates to a novel and efficient chemoenzymatic process of preparation of optically active trans alkyl phenylglycidates. The invention particularly discloses a novel process for the chemoenzymatic synthesis of two enantiomers of trans alkyl phenylglycidate i.e. alkyl(2S,3R)-phenylglycidate and alkyl(2R,3S)-phenylglycidate of formulae 7 and 8 respectively.
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