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3-acetyl-1-benzyl-4-phenylquinolin-2(1H)-one | 1360567-01-6

中文名称
——
中文别名
——
英文名称
3-acetyl-1-benzyl-4-phenylquinolin-2(1H)-one
英文别名
3-acetyl-1-benzyl-4-phenylquinolin-2-one
3-acetyl-1-benzyl-4-phenylquinolin-2(1H)-one化学式
CAS
1360567-01-6
化学式
C24H19NO2
mdl
——
分子量
353.42
InChiKey
IEMLKMAKQDXJID-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):
    4.1
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 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:
    2-氨基二苯甲酮 在 Amberlite Na sr1L 作用下, 反应 0.16h, 生成 3-acetyl-1-benzyl-4-phenylquinolin-2(1H)-one
    参考文献:
    名称:
    Solvent-free synthesis and antibacterial studies of some quinolinones
    摘要:
    Solvent-free, microwave-induced condensation of 2-aminoaryl alkyl ketones and ethyl 3-oxobutanoate in the presence of amberlite Na sr1L gave quinolinones in high yield when compared to other catalysts. Further, N-alkylation of the quinolinones was carried out effectively with various halides using amberlite Na sr1L. An N-alkylated quinolinone exhibited enhanced activities against B. subtilis, E. coli, and P. aeruginosa, similar to standard drug ampicillin. Two compounds showed effective activity against S. aureus, and one resulted in moderate activity against E. coli.
    DOI:
    10.1007/s00706-011-0608-1
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文献信息

  • Solvent-free synthesis and antibacterial studies of some quinolinones
    作者:Radhakrishnan Subashini、Fazlur-Rahman Nawaz Khan
    DOI:10.1007/s00706-011-0608-1
    日期:2012.3
    Solvent-free, microwave-induced condensation of 2-aminoaryl alkyl ketones and ethyl 3-oxobutanoate in the presence of amberlite Na sr1L gave quinolinones in high yield when compared to other catalysts. Further, N-alkylation of the quinolinones was carried out effectively with various halides using amberlite Na sr1L. An N-alkylated quinolinone exhibited enhanced activities against B. subtilis, E. coli, and P. aeruginosa, similar to standard drug ampicillin. Two compounds showed effective activity against S. aureus, and one resulted in moderate activity against E. coli.
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