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3,5-bis(5,8-diamino-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)benzoic acid | 1354701-73-7

中文名称
——
中文别名
——
英文名称
3,5-bis(5,8-diamino-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)benzoic acid
英文别名
3,5-Bis(5,8-diamino-1,3-dioxobenzo[de]isoquinolin-2-yl)benzoic acid;3,5-bis(5,8-diamino-1,3-dioxobenzo[de]isoquinolin-2-yl)benzoic acid
3,5-bis(5,8-diamino-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)benzoic acid化学式
CAS
1354701-73-7
化学式
C31H20N6O6
mdl
——
分子量
572.536
InChiKey
ZRJDGVBNAQRPBF-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):
    2.3
  • 重原子数:
    43
  • 可旋转键数:
    3
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    216
  • 氢给体数:
    5
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    3,5-bis-(5,8-dinitro-1,3-dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-benzoic acid 在 palladium 10% on activated carbon 、 氢气 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 25.0 ℃ 、100.0 kPa 条件下, 反应 24.0h, 以89%的产率得到3,5-bis(5,8-diamino-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)benzoic acid
    参考文献:
    名称:
    The synthesis and fluorescence properties of macromolecular components based on 1,8-naphthalimide derivatives and dimers
    摘要:
    A series of novel 1,8-naphthalimide derivatives and dimers possessing reactive carboxylic acid, nitro, amine, or bromide functionality is prepared and their photophysical properties are studied. Those derivatives that contain amine substituents attached directly to the 1,8-naphthalimide unit display intense yellow-green fluorescence. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2011.12.009
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文献信息

  • The synthesis and fluorescence properties of macromolecular components based on 1,8-naphthalimide derivatives and dimers
    作者:Alaa M.M. El-Betany、Neil B. McKeown
    DOI:10.1016/j.tetlet.2011.12.009
    日期:2012.2
    A series of novel 1,8-naphthalimide derivatives and dimers possessing reactive carboxylic acid, nitro, amine, or bromide functionality is prepared and their photophysical properties are studied. Those derivatives that contain amine substituents attached directly to the 1,8-naphthalimide unit display intense yellow-green fluorescence. (C) 2011 Elsevier Ltd. All rights reserved.
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