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3-Methoxy-6,8-dimethyl-2-(p-chlorphenyl)-4-quinaldehyde | 57464-15-0

中文名称
——
中文别名
——
英文名称
3-Methoxy-6,8-dimethyl-2-(p-chlorphenyl)-4-quinaldehyde
英文别名
2-(4-chloro-phenyl)-3-methoxy-6,8-dimethyl-quinoline-4-carbaldehyde;Quinoline 4-formyl-3-methoxy-6,8-dimethyl-2-[4-chlrophenyl]-;2-(4-chlorophenyl)-3-methoxy-6,8-dimethylquinoline-4-carbaldehyde
3-Methoxy-6,8-dimethyl-2-(p-chlorphenyl)-4-quinaldehyde化学式
CAS
57464-15-0
化学式
C19H16ClNO2
mdl
——
分子量
325.795
InChiKey
ATGYVLQHBUTFDC-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):
    4.6
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    39.2
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    methylenedimethyl sulfurane3-Methoxy-6,8-dimethyl-2-(p-chlorphenyl)-4-quinaldehyde 生成 2-(4-chloro-phenyl)-3-methoxy-6,8-dimethyl-4-oxiranyl-quinoline
    参考文献:
    名称:
    Antimalarials. 10. Substituted 3-halo- and 3-methoxy-2-aryl-4-quinoline(dibutylaminomethyl)methanols
    摘要:
    Four 2-aryl-4-quinoline(di-n-butylaminomethyl)methanols with Br, Cl, F, or OMe in position 3 were synthesized by modifications of standard reactions. The antimalarial activity decreased with increased size of the 3-substituent. The 3-F-4',6,8-Cl3 compound was the most active (at 2.5 mg/kg) and was completely curative at 80 mg/kg against P. berghei in mice.
    DOI:
    10.1021/jm00246a012
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文献信息

  • Antimalarials. 10. Substituted 3-halo- and 3-methoxy-2-aryl-4-quinoline(dibutylaminomethyl)methanols
    作者:H. Randall Munson、Richard E. Johnson、J. Milton Sanders、Cyrus J. Ohnmacht、Robert E. Lutz
    DOI:10.1021/jm00246a012
    日期:1975.12
    Four 2-aryl-4-quinoline(di-n-butylaminomethyl)methanols with Br, Cl, F, or OMe in position 3 were synthesized by modifications of standard reactions. The antimalarial activity decreased with increased size of the 3-substituent. The 3-F-4',6,8-Cl3 compound was the most active (at 2.5 mg/kg) and was completely curative at 80 mg/kg against P. berghei in mice.
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