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Zn(II)-5,15-bis(4-hydroxyphenyl)-10,20-bis(4-cyanophenyl)porphyrin | 1252590-45-6

中文名称
——
中文别名
——
英文名称
Zn(II)-5,15-bis(4-hydroxyphenyl)-10,20-bis(4-cyanophenyl)porphyrin
英文别名
——
Zn(II)-5,15-bis(4-hydroxyphenyl)-10,20-bis(4-cyanophenyl)porphyrin化学式
CAS
1252590-45-6
化学式
C46H26N6O2Zn
mdl
——
分子量
760.141
InChiKey
XXSUJBHQVWKZSX-XZWYRLAVSA-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:
    Zn(II)-5,15-bis(4-hydroxyphenyl)-10,20-bis(4-cyanophenyl)porphyrin三乙二醇单对甲苯磺酸酯caesium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 26.0h, 以57.5%的产率得到Zn(II)-5,15-bis(4-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)phenyl)-10,20-bis(4-cyanophenyl)porphyrin
    参考文献:
    名称:
    Boronic Acid Porphyrin Receptor for Ginsenoside Sensing
    摘要:
    Ginsenoside detection was pursued through the design of a porphyrin receptor containing two boronic acid units. This receptor was found to undergo different degrees of fluorescence quenching with five ginsenoside guests and an acylated derivative. The trends in the 1:1 binding constants, as well as ESI-HRMS analysis, support a binding mode in which the ginsenoside sugar units are bound to the boronic acid groups, while the steroid core and porphyrin ring participate in hydrophobic interactions.
    DOI:
    10.1021/ol1019647
  • 作为产物:
    描述:
    zinc diacetate 作用下, 以 甲醇氯仿 为溶剂, 反应 0.5h, 以421.5 mg的产率得到Zn(II)-5,15-bis(4-hydroxyphenyl)-10,20-bis(4-cyanophenyl)porphyrin
    参考文献:
    名称:
    Boronic Acid Porphyrin Receptor for Ginsenoside Sensing
    摘要:
    Ginsenoside detection was pursued through the design of a porphyrin receptor containing two boronic acid units. This receptor was found to undergo different degrees of fluorescence quenching with five ginsenoside guests and an acylated derivative. The trends in the 1:1 binding constants, as well as ESI-HRMS analysis, support a binding mode in which the ginsenoside sugar units are bound to the boronic acid groups, while the steroid core and porphyrin ring participate in hydrophobic interactions.
    DOI:
    10.1021/ol1019647
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