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4-[(Butylamino)methyl]-2,6-dimethoxyphenol | 112520-77-1

中文名称
——
中文别名
——
英文名称
4-[(Butylamino)methyl]-2,6-dimethoxyphenol
英文别名
4-(butylaminomethyl)-2,6-dimethoxyphenol
4-[(Butylamino)methyl]-2,6-dimethoxyphenol化学式
CAS
112520-77-1
化学式
C13H21NO3
mdl
MFCD11157770
分子量
239.315
InChiKey
JCTCMVJBWUPTGE-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:
    356.9±37.0 °C(Predicted)
  • 密度:
    1.054±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    17
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.538
  • 拓扑面积:
    50.7
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    4-[(Butylamino)methyl]-2,6-dimethoxyphenol 在 potassium nitrososulfonate 、 sodium dihydrogen phosphate disodium hydrogenphosphate 作用下, 以 氯仿 为溶剂, 以98%的产率得到2,6-二甲氧基-1,4-苯醌
    参考文献:
    名称:
    Fremy's 盐促进对羟基苯甲胺和对羟基苯甲酰胺的氧化降解。一种新的方法 top-醌
    摘要:
    对羟基苄胺和伯对羟基苯甲酰胺在弗雷米盐的作用下发生氧化降解,从而以良好的收率提供对苯醌。
    DOI:
    10.1246/cl.1987.771
  • 作为产物:
    描述:
    参考文献:
    名称:
    Benzylamine antioxidants: relationship between structure, peroxyl radical scavenging, lipid peroxidation inhibition and cytoprotection
    摘要:
    Three homologous series of 3,5-dialkoxy-4-hydroxybenzylamines were prepared and tested (1) as peroxyl radical scavengers in homogeneous aqueous solution, (2) as inhibitors of iron-dependent peroxidation of rabbit brain vesicular membrane lipids, and (3) as cytoprotective agents using primary cultures of rat hippocampal neurons exposed to hydrogen peroxide. The structural requirements for efficient radical trapping in homogeneous solution differed from those for effective lipid peroxidation inhibition: In homogeneous solution a kinetic preference existed for smaller, less sterically encumbered substituents flanking the reactive phenolic hydroxyl group. Lipid peroxidation inhibition, on the other hand, required longer more lipophilic substituents. Consequently, a lipophilic alkoxyl substituent at C3 and a small substituent at C5 appeared optimal for efficient radical scavenging activity in both lipid and homogeneous solution. Maximal cytoprotection of rat hippocampal neurons exposed to hydrogen peroxide was also associated with more lipophilic derivatives although substituent length and substituent bulk may represent independent parameters for relating structure and efficacy in this system.
    DOI:
    10.1021/jm00061a018
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文献信息

  • SAA J. M.; LLOBERA A.; DEYA P. M., CHEM. LETT.,(1987) N 5, 771-774
    作者:SAA J. M.、 LLOBERA A.、 DEYA P. M.
    DOI:——
    日期:——
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