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6-chloro-2-(4-methylphenyl)thiochromen-4-one | 1402911-80-1

中文名称
——
中文别名
——
英文名称
6-chloro-2-(4-methylphenyl)thiochromen-4-one
英文别名
6-Chloro-2-(4-methylphenyl)thiochromen-4-one
6-chloro-2-(4-methylphenyl)thiochromen-4-one化学式
CAS
1402911-80-1
化学式
C16H11ClOS
mdl
——
分子量
286.782
InChiKey
KZCRHTOGOGFKLO-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):
    4.7
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2,5-二氯苯乙酮 、 sodium hydride 、 碳酸氢钠 、 sodium hydroxide 作用下, 以 N-甲基吡咯烷酮乙醇N,N-二甲基甲酰胺 、 mineral oil 为溶剂, 反应 25.0h, 生成 6-chloro-2-(4-methylphenyl)thiochromen-4-one
    参考文献:
    名称:
    A Convenient Synthesis of 2-Arylthiochromen-4-ones (Thioflavones) by Iodine-Mediated Cyclization of 3-Aryl-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1-ones
    摘要:
    A convenient two-step synthesis of 2-arylthiochromen-4-ones (thioflavones) beginning with 1-[2-(1,1-dimethylethylsulfanyl)phenyl]ethanones is described. Thus, 3-aryl-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1-ones were prepared by the condensation of 1-[2-(1,1-dimethylethylsulfanyl)phenyl]ethanones with aromatic aldehyde in the presence of sodium hydroxide, and were treated with iodine in refluxing N-methylpyrrolidin-2-one (NMP) or propanenitrile to afford the desired products in moderate to fair yields.
    DOI:
    10.3987/com-12-12508
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文献信息

  • A Convenient Synthesis of 2-Arylthiochromen-4-ones (Thioflavones) by Iodine-Mediated Cyclization of 3-Aryl-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1-ones
    作者:Kazuhiro Kobayashi、Akihiro Kobayashi、Kosuke Ezaki
    DOI:10.3987/com-12-12508
    日期:——
    A convenient two-step synthesis of 2-arylthiochromen-4-ones (thioflavones) beginning with 1-[2-(1,1-dimethylethylsulfanyl)phenyl]ethanones is described. Thus, 3-aryl-1-[2-(1,1-dimethylethylsulfanyl)phenyl]prop-2-en-1-ones were prepared by the condensation of 1-[2-(1,1-dimethylethylsulfanyl)phenyl]ethanones with aromatic aldehyde in the presence of sodium hydroxide, and were treated with iodine in refluxing N-methylpyrrolidin-2-one (NMP) or propanenitrile to afford the desired products in moderate to fair yields.
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