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| 1239518-10-5

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1239518-10-5
化学式
C74H64ClFeN10O5
mdl
——
分子量
1264.69
InChiKey
ULYXDHWVTMDRBR-ACOYPIRTSA-L
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:
    、 copper diacetate 以 乙醇乙腈 为溶剂, 以99%的产率得到
    参考文献:
    名称:
    Spectroscopic and electrochemical studies of novel model compounds for cytochrome c oxidase
    摘要:
    Different metalated porphyrin compounds were studied as model complexes for cytochrome c oxidase. All models contain a tyrosine molecule and a copper binding site. Two of the compounds are bearing an axial pyridine ligand that could possibly coordinate with Fe porphyrins. All complexes were studied using NMR and UV-Vis spectroscopies and it was found that the coordination of the axial ligand is possible only in one of the porphyrins. Moreover, the synthesized catalysts were studied as promising enzyme mimics using a rotating disc electrode in the presence of molecular oxygen. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2010.03.026
  • 作为产物:
    描述:
    在 iron(II) bromide 作用下, 以 四氢呋喃 为溶剂, 反应 12.0h, 以82%的产率得到
    参考文献:
    名称:
    Spectroscopic and electrochemical studies of novel model compounds for cytochrome c oxidase
    摘要:
    Different metalated porphyrin compounds were studied as model complexes for cytochrome c oxidase. All models contain a tyrosine molecule and a copper binding site. Two of the compounds are bearing an axial pyridine ligand that could possibly coordinate with Fe porphyrins. All complexes were studied using NMR and UV-Vis spectroscopies and it was found that the coordination of the axial ligand is possible only in one of the porphyrins. Moreover, the synthesized catalysts were studied as promising enzyme mimics using a rotating disc electrode in the presence of molecular oxygen. (C) 2010 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.ica.2010.03.026
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