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8-methoxy-2-(4,8-dimethoxynaphthalen-1-ylamino)-1,4-naphthoquinone | 1223146-47-1

中文名称
——
中文别名
——
英文名称
8-methoxy-2-(4,8-dimethoxynaphthalen-1-ylamino)-1,4-naphthoquinone
英文别名
2-[(4,8-Dimethoxynaphthalen-1-yl)amino]-8-methoxynaphthalene-1,4-dione;2-[(4,8-dimethoxynaphthalen-1-yl)amino]-8-methoxynaphthalene-1,4-dione
8-methoxy-2-(4,8-dimethoxynaphthalen-1-ylamino)-1,4-naphthoquinone化学式
CAS
1223146-47-1
化学式
C23H19NO5
mdl
——
分子量
389.408
InChiKey
KZMMZUKTBXLJAJ-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):
    4.4
  • 重原子数:
    29
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    73.9
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    4,8-dimethoxy-1-naphthylamine氧气dioxide titanium 作用下, 以 乙腈 为溶剂, 反应 4.0h, 以40%的产率得到8-methoxy-2-(4,8-dimethoxynaphthalen-1-ylamino)-1,4-naphthoquinone
    参考文献:
    名称:
    Oxidative Dimerization of 4-Methoxynaphthylamines in the Presence of Semiconductors
    摘要:
    Three types of 4-methoxynaphthylamines 4a-c were oxidized by treatment with metal oxides under molecular oxygen (02). 4-Methoxy-1-naphthylamine 4a and 4,6-dimethoxy-1-naphthylamine 4b, on treatment with TiO(2) under O(2), gave mainly 2-amino-1,4-naphthoquinone derivatives 5a and 5b, respectively whereas 4,8-dimethoxy-1-naphthylamine 4c afforded an unique carbazole 6c as the major product.
    DOI:
    10.3987/com-09-s(s)107
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文献信息

  • Oxidative Dimerization of 4-Methoxynaphthylamines in the Presence of Semiconductors
    作者:Osamu Tamura、Tetsuya Takeya、Yosuke Takahashi、Iwao Okamoto
    DOI:10.3987/com-09-s(s)107
    日期:——
    Three types of 4-methoxynaphthylamines 4a-c were oxidized by treatment with metal oxides under molecular oxygen (02). 4-Methoxy-1-naphthylamine 4a and 4,6-dimethoxy-1-naphthylamine 4b, on treatment with TiO(2) under O(2), gave mainly 2-amino-1,4-naphthoquinone derivatives 5a and 5b, respectively whereas 4,8-dimethoxy-1-naphthylamine 4c afforded an unique carbazole 6c as the major product.
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