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1-[3-(1,4-dihydro-3-hydroxy-1,4-dioxonaphthalen-2-yl-oxy)phenyl]-5,6-dihydro-6-methylpyrimidine-2,4(1H,3H)-dione | 1310679-99-2

中文名称
——
中文别名
——
英文名称
1-[3-(1,4-dihydro-3-hydroxy-1,4-dioxonaphthalen-2-yl-oxy)phenyl]-5,6-dihydro-6-methylpyrimidine-2,4(1H,3H)-dione
英文别名
1-[3-(1,4-Dihydro-3-hydroxy-1,4-dioxonaphthalen-2-yloxy)phenyl]-5,6-dihydro-6-methylpyrimidine-2,4(1h,3h)-dione;1-[3-(3-hydroxy-1,4-dioxonaphthalen-2-yl)oxyphenyl]-6-methyl-1,3-diazinane-2,4-dione
1-[3-(1,4-dihydro-3-hydroxy-1,4-dioxonaphthalen-2-yl-oxy)phenyl]-5,6-dihydro-6-methylpyrimidine-2,4(1H,3H)-dione化学式
CAS
1310679-99-2
化学式
C21H16N2O6
mdl
——
分子量
392.368
InChiKey
GXUPDCYURAEMHU-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):
    2.2
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    113
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    1,1'-[(1,4-dihydro-1,4-dioxo-2,3-naphthalenediyl)bis-(oxy-3,1-phenylene)]bis(5,6-dihydro-6-methylpyrimidine-2,4(1H,3H)-dione) 在 盐酸 、 sodium hydroxide 作用下, 以 为溶剂, 反应 3.0h, 生成 1-[3-(1,4-dihydro-3-hydroxy-1,4-dioxonaphthalen-2-yl-oxy)phenyl]-5,6-dihydro-6-methylpyrimidine-2,4(1H,3H)-dione
    参考文献:
    名称:
    Synthesis, chemical properties, and antimicrobial activity of 2- and 2,3-substituted [(tetrahydro-2,4-dioxopyrimidin-1(2H)-yl)phenoxy]naphthalene-1,4-diones
    摘要:
    Mono- and disubstituted [(tetrahydro-2,4-dioxopyrimidin-1(2H)-yl)phenoxy]naphthalene-1,4-diones were synthesized by the reaction of dihydro-1-(3-hydroxy- and 4-hydroxyphenyl)pyrimidine-2,4(1H,3H)-diones and their 5- and 6-methyl derivatives with 2,3-dichloro-1,4-naphthoquinone. Their stability in alkaline and acidic media was investigated. Four of the compounds exhibited good antimicrobial activity against Staphylococcus aureus, Mycobacterium luteum, Candida tenuis, and Aspergillus niger.
    DOI:
    10.1007/s00706-011-0466-x
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文献信息

  • Synthesis, chemical properties, and antimicrobial activity of 2- and 2,3-substituted [(tetrahydro-2,4-dioxopyrimidin-1(2H)-yl)phenoxy]naphthalene-1,4-diones
    作者:Aušra Voskienė、Birutė Sapijanskaitė、Vytautas Mickevičius、Kristina Kantminienė、Maryna Stasevych、Olena Komarovska-Porokhnyavets、Rostyslav Musyanovych、Volodymyr Novikov
    DOI:10.1007/s00706-011-0466-x
    日期:2011.5
    Mono- and disubstituted [(tetrahydro-2,4-dioxopyrimidin-1(2H)-yl)phenoxy]naphthalene-1,4-diones were synthesized by the reaction of dihydro-1-(3-hydroxy- and 4-hydroxyphenyl)pyrimidine-2,4(1H,3H)-diones and their 5- and 6-methyl derivatives with 2,3-dichloro-1,4-naphthoquinone. Their stability in alkaline and acidic media was investigated. Four of the compounds exhibited good antimicrobial activity against Staphylococcus aureus, Mycobacterium luteum, Candida tenuis, and Aspergillus niger.
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