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2-(3,4-dihydroxy-5-methoxyphenyl)acetic acid | 2989-10-8

中文名称
——
中文别名
——
英文名称
2-(3,4-dihydroxy-5-methoxyphenyl)acetic acid
英文别名
(3,4-dihydroxy-5-methoxy-phenyl)-acetic acid;(3,4-Dihydroxy-5-methoxy-phenyl)-essigsaeure;3,4-Dihydroxy-5-methoxy-phenylessigsaeure
2-(3,4-dihydroxy-5-methoxyphenyl)acetic acid化学式
CAS
2989-10-8
化学式
C9H10O5
mdl
——
分子量
198.175
InChiKey
RGHMGZLQQFVXDM-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:
    132-134 °C(Solv: ethyl acetate (141-78-6); ligroine (8032-32-4))
  • 沸点:
    446.5±40.0 °C(Predicted)
  • 密度:
    1.438±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    14
  • 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:
    87
  • 氢给体数:
    3
  • 氢受体数:
    5

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

反应信息

  • 作为产物:
    描述:
    高香草酸 在 Agaricus bisporus 、 氧气 作用下, 以 aq. phosphate buffer 、 二氯甲烷 为溶剂, 反应 24.0h, 以98%的产率得到2-(3,4-dihydroxy-5-methoxyphenyl)acetic acid
    参考文献:
    名称:
    Tyrosinase and Layer-by-Layer supported tyrosinases in the synthesis of lipophilic catechols with antiinfluenza activity
    摘要:
    Catechol derivatives with lipophilic properties have been selectively synthesized by tyrosinase in high yield avoiding long and tedious protection/deprotection steps usually required in traditional procedures. The synthesis was effective also with immobilized tyrosinase able to perform for more runs. The novel catechols were evaluated against influenza A virus, that continue to represent a severe threat worldwide. A significant antiviral activity was observed in derivatives characterized by antioxidant activity and long carbon alkyl side-chains, suggesting the possibility of a new inhibition mechanism based on both redox and lipophilic properties. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2013.10.026
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文献信息

  • Kimura, Yasuo; Nishibe, Masahiko; Nakajima, Hiromitsu, Agricultural and Biological Chemistry, 1991, vol. 55, # 4, p. 1137 - 1138
    作者:Kimura, Yasuo、Nishibe, Masahiko、Nakajima, Hiromitsu、Hamasaki, Takashi
    DOI:——
    日期:——
  • 525. Synthesis of 3 : 4-dihydroxy-5-methoxyphenylacetic acid, a metabolite of mescaline in man
    作者:John Harley-Mason、A. H. Laird
    DOI:10.1039/jr9590002629
    日期:——
  • Liquid crystalline optical film, compensating film for liquid crystal display and liquid crystal display
    申请人:NIPPON OIL COMPANY, LIMITED
    公开号:EP0758013B1
    公开(公告)日:2000-10-11
  • US5855971A
    申请人:——
    公开号:US5855971A
    公开(公告)日:1999-01-05
  • Tyrosinase and Layer-by-Layer supported tyrosinases in the synthesis of lipophilic catechols with antiinfluenza activity
    作者:Tiziana Bozzini、Giorgia Botta、Michela Delfino、Silvano Onofri、Raffaele Saladino、Donatella Amatore、Rossella Sgarbanti、Lucia Nencioni、Anna Teresa Palamara
    DOI:10.1016/j.bmc.2013.10.026
    日期:2013.12
    Catechol derivatives with lipophilic properties have been selectively synthesized by tyrosinase in high yield avoiding long and tedious protection/deprotection steps usually required in traditional procedures. The synthesis was effective also with immobilized tyrosinase able to perform for more runs. The novel catechols were evaluated against influenza A virus, that continue to represent a severe threat worldwide. A significant antiviral activity was observed in derivatives characterized by antioxidant activity and long carbon alkyl side-chains, suggesting the possibility of a new inhibition mechanism based on both redox and lipophilic properties. (C) 2013 Elsevier Ltd. All rights reserved.
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