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2-(4-Methoxyphenyl)-3,6-dimethyl-2,3-dihydrochromen-4-one | 1403356-73-9

中文名称
——
中文别名
——
英文名称
2-(4-Methoxyphenyl)-3,6-dimethyl-2,3-dihydrochromen-4-one
英文别名
——
2-(4-Methoxyphenyl)-3,6-dimethyl-2,3-dihydrochromen-4-one化学式
CAS
1403356-73-9
化学式
C18H18O3
mdl
——
分子量
282.339
InChiKey
RFSSRRSBNGDHPF-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):
    3.8
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-(4-Methoxyphenyl)-3,6-dimethyl-2,3-dihydrochromen-4-one硫酸二甲基亚砜 作用下, 反应 0.5h, 以89%的产率得到
    参考文献:
    名称:
    Efficient Synthesis of 3-Methyl-Flavanones and Evaluation of Their Anti-Bacterial Activity
    摘要:
    AbstractA series of 2‐phenyl‐2,3‐dihydrochromon‐4‐one derivatives (flavanone derivatives) were synthesized by silica gel assisted isomerization of several α‐methyl‐2′‐hydroxy chalcones in 74%–88% yield. These flavanones were further oxidized to 3‐methyl flavones by using iodine in dimethyl sulphoxide at 60°C in presence of acid. The newly synthesized derivatives were evaluated for in vitro study against Staphylococcus aureus, Micrococcus luteus and Staphylococcus epidermis.
    DOI:
    10.1002/cjoc.201200254
  • 作为产物:
    描述:
    在 adsorbed H2SO4 on silica gel 作用下, 以 二氯甲烷 为溶剂, 反应 3.0h, 以86%的产率得到2-(4-Methoxyphenyl)-3,6-dimethyl-2,3-dihydrochromen-4-one
    参考文献:
    名称:
    Efficient Synthesis of 3-Methyl-Flavanones and Evaluation of Their Anti-Bacterial Activity
    摘要:
    AbstractA series of 2‐phenyl‐2,3‐dihydrochromon‐4‐one derivatives (flavanone derivatives) were synthesized by silica gel assisted isomerization of several α‐methyl‐2′‐hydroxy chalcones in 74%–88% yield. These flavanones were further oxidized to 3‐methyl flavones by using iodine in dimethyl sulphoxide at 60°C in presence of acid. The newly synthesized derivatives were evaluated for in vitro study against Staphylococcus aureus, Micrococcus luteus and Staphylococcus epidermis.
    DOI:
    10.1002/cjoc.201200254
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