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N-(3-hydroxy-4-methoxybenzyl)-2,4,6-trihydroxybenzamide | 76820-15-0

中文名称
——
中文别名
——
英文名称
N-(3-hydroxy-4-methoxybenzyl)-2,4,6-trihydroxybenzamide
英文别名
2,4,6-trihydroxy-N-[(3-hydroxy-4-methoxyphenyl)methyl]benzamide
N-(3-hydroxy-4-methoxybenzyl)-2,4,6-trihydroxybenzamide化学式
CAS
76820-15-0
化学式
C15H15NO6
mdl
——
分子量
305.287
InChiKey
XMIPBMBAYILFBS-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

  • 沸点:
    630.5±55.0 °C(Predicted)
  • 密度:
    1.466±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    119
  • 氢给体数:
    5
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    N-(3-hydroxy-4-methoxybenzyl)-2,4,6-trihydroxybenzamide吡啶potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 40.0h, 生成 N-(3-hydroxy-4-methoxybenzyl)-5-hydroxy-7-(carbethoxymethoxy)-3,4-dihydro-2H-1,3-benzoxazine-2,4-dione
    参考文献:
    名称:
    Dihydrochalcone sweeteners. A study of the atypical temporal phenomena
    摘要:
    Neohesperidin dihydrochalcone (NHDHC), known since 1963 as an intensely sweet compound, is determined to be 340 +/- 60 (p less than 0.05) times more potent than sucrose. The unusual temporal properties of this material are hypothesized as being due to the effects of metabolism, conformation, chelation, or hydrophobicity. Forty-four analogues are synthesized to test the four hypotheses, none of which are strongly supported. A method of quantitation of temporal characteristics of tastant molecules is developed so as to allow comparison of taste appearance time (AT) and extinction time (ET) of experimental compounds. Four of the new compounds, 40 and 43-45, exhibit high sweetness potencies, ranging from 280 and 440 times sucrose, and may be useful in selected food systems. The temporal taste characteristics remain unimproved over NHDHC, however.
    DOI:
    10.1021/jm00136a011
  • 作为产物:
    描述:
    1,3,5-三(苯基甲氧基)苯 在 palladium on activated charcoal 氢氧化钾氢气 、 sodium hydride 作用下, 以 四氢呋喃乙醚二氯甲烷乙酸乙酯 为溶剂, 25.0 ℃ 、101.33 kPa 条件下, 反应 46.0h, 生成 N-(3-hydroxy-4-methoxybenzyl)-2,4,6-trihydroxybenzamide
    参考文献:
    名称:
    Dihydrochalcone sweeteners. A study of the atypical temporal phenomena
    摘要:
    Neohesperidin dihydrochalcone (NHDHC), known since 1963 as an intensely sweet compound, is determined to be 340 +/- 60 (p less than 0.05) times more potent than sucrose. The unusual temporal properties of this material are hypothesized as being due to the effects of metabolism, conformation, chelation, or hydrophobicity. Forty-four analogues are synthesized to test the four hypotheses, none of which are strongly supported. A method of quantitation of temporal characteristics of tastant molecules is developed so as to allow comparison of taste appearance time (AT) and extinction time (ET) of experimental compounds. Four of the new compounds, 40 and 43-45, exhibit high sweetness potencies, ranging from 280 and 440 times sucrose, and may be useful in selected food systems. The temporal taste characteristics remain unimproved over NHDHC, however.
    DOI:
    10.1021/jm00136a011
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文献信息

  • Hydroxybenzoic Acid Amides and the Use Thereof For Masking Bitter Taste
    申请人:Ley Jakob
    公开号:US20080214675A1
    公开(公告)日:2008-09-04
    The use is described of hydroxybenzoic acid amides having formula (I) wherein R 1 to R 5 mutually independently denote hydrogen, hydroxy, methoxy or ethoxy, with the proviso that at least one of the radicals R 1 to R 5 denotes hydroxy. and R 6 denotes hydrogen, methyl or ethyl and n denotes 1 or 2, their salts and mixtures thereof, to mask or reduce the unpleasant flavour impression of an unpleasantly tasting substance and/or to strengthen the sweet flavour impression of a sweet substance.
  • Dihydrochalcone sweeteners. A study of the atypical temporal phenomena
    作者:Grant E. DuBois、Guy A. Crosby、Rebecca A. Stephenson
    DOI:10.1021/jm00136a011
    日期:1981.4
    Neohesperidin dihydrochalcone (NHDHC), known since 1963 as an intensely sweet compound, is determined to be 340 +/- 60 (p less than 0.05) times more potent than sucrose. The unusual temporal properties of this material are hypothesized as being due to the effects of metabolism, conformation, chelation, or hydrophobicity. Forty-four analogues are synthesized to test the four hypotheses, none of which are strongly supported. A method of quantitation of temporal characteristics of tastant molecules is developed so as to allow comparison of taste appearance time (AT) and extinction time (ET) of experimental compounds. Four of the new compounds, 40 and 43-45, exhibit high sweetness potencies, ranging from 280 and 440 times sucrose, and may be useful in selected food systems. The temporal taste characteristics remain unimproved over NHDHC, however.
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