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methyl (E)-3-(4,5-dihydroxy-2-nitrophenyl)propenoate

中文名称
——
中文别名
——
英文名称
methyl (E)-3-(4,5-dihydroxy-2-nitrophenyl)propenoate
英文别名
methyl 2-nitrocaffeate;methyl (E)-3-(4,5-dihydroxy-2-nitrophenyl)prop-2-enoate
methyl (E)-3-(4,5-dihydroxy-2-nitrophenyl)propenoate化学式
CAS
——
化学式
C10H9NO6
mdl
——
分子量
239.185
InChiKey
JZOXXMGGAKNWJW-NSCUHMNNSA-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):
    1.3
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    113
  • 氢给体数:
    2
  • 氢受体数:
    6

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:
    参考文献:
    名称:
    Reaction of caffeic acid derivatives with acidic nitrite
    摘要:
    Caffeic derivatives were reacted with acidic nitrite at controlled pH in order to mimic the gastric juice conditions. At pH 2, whereas caffeic acid reacts exclusively on the side chain, its esters are readily nitrated. Under more acidic conditions (pH 1), caffeic acid methyl ester undergoes a dimerisation into a norlignan derivative. (C) 2001 Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4039(01)00441-5
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文献信息

  • New Insights into the Acid-Promoted Reaction of Caffeic Acid and Its Esters with Nitrite:  Decarboxylation Drives Chain Nitrosation Pathways toward Novel Oxime Derivatives and Oxidation/Fragmentation Products Thereof
    作者:Alessandra Napolitano、Marco d'Ischia
    DOI:10.1021/jo015965v
    日期:2002.2.1
    methyl ester (1b) reacted with NO(2)(-) chiefly via ring nitration and/or dimerization to give 5a, the novel nitrated neolignan derivative 10, and the parent 6. Chlorogenic acid (1c) afforded only the ring nitrated derivative 5b. A unifying mechanism for the reaction of 1a and its esters with NO(2)(-) is proposed involving reversible formation of nitroso intermediates via chain nitrosation at the 2-position
    在含有1%甲醇的0.05 M醋酸盐缓冲液(pH 4)中,咖啡酸(1a)(2 x 10(-3)M)与亚硝酸盐(NO(2)(-))(4 x 10(-3)平稳反应M)作为主要产品提供较小的新型2-羟基-和2-甲氧基醛肟7a,b,2-环氧醛肟9a,3,4-二羟基苯甲酸,3,4-二羟基苯甲醛和已知的呋喃喃3c和苯并恶嗪酮4b金额。在较低的1a浓度下(例如1 x 10(-4)M),主要产物为7a,而0.1 m 1a和0.5 M NO(2)(-)3c和9a为主要产物。在pH 2时,7a与3,4-二羟基苯甲醛和一些9a仍然是最丰富的产物,而在pH 1时,9a和3,4-二羟基苯甲醛的产率更高。没有获得关于环硝化产物的证据,包括先前报道的4,5-二羟基-2-硝基苯甲醛。在2 x 10(-3)M浓度和pH 4下 咖啡酸甲酯(1b)主要通过环硝化和/或二聚反应与NO(2)(-)反应生成5a,新型硝化的新木脂素衍生
  • Reaction of caffeic acid derivatives with acidic nitrite
    作者:Philippe Cotelle、Hervé Vezin
    DOI:10.1016/s0040-4039(01)00441-5
    日期:2001.5
    Caffeic derivatives were reacted with acidic nitrite at controlled pH in order to mimic the gastric juice conditions. At pH 2, whereas caffeic acid reacts exclusively on the side chain, its esters are readily nitrated. Under more acidic conditions (pH 1), caffeic acid methyl ester undergoes a dimerisation into a norlignan derivative. (C) 2001 Published by Elsevier Science Ltd.
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