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2-(3-ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydroquinolin-6-yl)-5,10,15,20-tetraphenylporphyrinatozinc(II) | 1334214-69-5

中文名称
——
中文别名
——
英文名称
2-(3-ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydroquinolin-6-yl)-5,10,15,20-tetraphenylporphyrinatozinc(II)
英文别名
——
2-(3-ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydroquinolin-6-yl)-5,10,15,20-tetraphenylporphyrinatozinc(II)化学式
CAS
1334214-69-5
化学式
C58H41N5O3Zn
mdl
——
分子量
921.385
InChiKey
ARKJAXKQQVQRRD-TUDMZQQBSA-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    2-(3-ethoxycarbonyl-1-ethyl-4-oxo-1,4-dihydroquinolin-6-yl)-5,10,15,20-tetraphenylporphyrinatozinc(II)吡啶三氟乙酸 、 potassium hydroxide 作用下, 以 四氢呋喃甲醇氯仿 为溶剂, 反应 1.03h, 生成 2-(3-carboxy-1-ethyl-4-oxo-1,4-dihydroquinolin-6-yl)-5,10,15,20-tetraphenylporphyrin
    参考文献:
    名称:
    Synthesis and characterization of new porphyrin/4-quinolone conjugates
    摘要:
    New porphyrin/4-quinolone conjugates were synthesized from the Suzuki-Miyaura coupling reaction of a beta-borylated porphyrin with bromo-4-quinolones containing N-ethyl and N-D-ribofuranosyl substituents. The use of electrospray ionization tandem mass spectrometry showed important information about the fragmentation pathways of the new compounds. It was possible to distinguish between those compounds with the porphyrin moiety linked at the 6-position of the quinolone unit from their 7-substituted isomers. The new compounds showed to be good singlet oxygen generators. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.07.025
  • 作为产物:
    参考文献:
    名称:
    Synthesis and characterization of new porphyrin/4-quinolone conjugates
    摘要:
    New porphyrin/4-quinolone conjugates were synthesized from the Suzuki-Miyaura coupling reaction of a beta-borylated porphyrin with bromo-4-quinolones containing N-ethyl and N-D-ribofuranosyl substituents. The use of electrospray ionization tandem mass spectrometry showed important information about the fragmentation pathways of the new compounds. It was possible to distinguish between those compounds with the porphyrin moiety linked at the 6-position of the quinolone unit from their 7-substituted isomers. The new compounds showed to be good singlet oxygen generators. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.07.025
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