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N-hexyl-4-hydroxycinnamamide

中文名称
——
中文别名
——
英文名称
N-hexyl-4-hydroxycinnamamide
英文别名
N-hexyl-3-(4-hydroxyphenyl)prop-2-enamide
N-hexyl-4-hydroxycinnamamide化学式
CAS
——
化学式
C15H21NO2
mdl
——
分子量
247.337
InChiKey
GWEYIZUAQPNBAO-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    18
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    49.3
  • 氢给体数:
    2
  • 氢受体数:
    2

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:
    正己胺对羟基肉桂酸 在 Candida antarctica lipase 作用下, 以75.6%的产率得到N-hexyl-4-hydroxycinnamamide
    参考文献:
    名称:
    Lipase-Catalyzed Solvent-Free Amidation of Phenolic Acids
    摘要:
    A series of N-alkyl-substituted amides, based on various phenolic acids, have been synthesized by the condensation of equimolar amounts of phenolic acids with different alkyl amines in the presence of Candida antarctica lipase at 60-90 degrees C in 16-20 h. The reactions were carried out in a solvent-free system without the use of any activating agents. All the products were obtained in appreciable amounts and the yields for different compounds varied between 75.6% and 83.5%. The synthesized compounds were characterized using spectroscopy techniques, namely infrared and NMR (H-1 and C-13).
    DOI:
    10.1080/00397911.2014.974611
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文献信息

  • Lipase-Catalyzed Solvent-Free Amidation of Phenolic Acids
    作者:Parshant Kaushik、Najam Akhtar Shakil、Jitendra Kumar、Braj Bhushan Singh
    DOI:10.1080/00397911.2014.974611
    日期:2015.3.4
    A series of N-alkyl-substituted amides, based on various phenolic acids, have been synthesized by the condensation of equimolar amounts of phenolic acids with different alkyl amines in the presence of Candida antarctica lipase at 60-90 degrees C in 16-20 h. The reactions were carried out in a solvent-free system without the use of any activating agents. All the products were obtained in appreciable amounts and the yields for different compounds varied between 75.6% and 83.5%. The synthesized compounds were characterized using spectroscopy techniques, namely infrared and NMR (H-1 and C-13).
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