210769-64-5

Basic information

• Product Name: PentaMethylene Bis[4-(10,15,20-triphenylporphyrin-5-yl)benzoate]dizinc(II) [Reagent for application of the exciton chirality Method]
• Synonyms: PentaMethylene Bis[4-(10,15,20-triphenylporphyrin-5-yl)benzoate]dizinc(II) [Reagent for application of the exciton chirality Method]
• CAS NO: 210769-64-5
• Molecular Formula: C₉₅H₆₄N₈O₄Zn₂
• Molecular Weight: 1512.35586
• Mol File: 210769-64-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 0-10°C
• CAS DataBase Reference: PentaMethylene Bis[4-(10,15,20-triphenylporphyrin-5-yl)benzoate]dizinc(II) [Reagent for application of the exciton chirality Method](CAS DataBase Reference)
• NIST Chemistry Reference: PentaMethylene Bis[4-(10,15,20-triphenylporphyrin-5-yl)benzoate]dizinc(II) [Reagent for application of the exciton chirality Method](210769-64-5)
• EPA Substance Registry System: PentaMethylene Bis[4-(10,15,20-triphenylporphyrin-5-yl)benzoate]dizinc(II) [Reagent for application of the exciton chirality Method](210769-64-5)

Safety Data

• Hazardous Substances Data: 210769-64-5(Hazardous Substances Data)

Upstream product

• 7646-85-7 zinc(II) chloride 
• 111-29-5 1 ,5-pentanediol 
• 95051-10-8 5-(4-carboxyphenyl)-10,15,20-triphenyl-21H,23H-porphyrin 
• 557-34-6 zinc diacetate 

Downstream Products

• 1146196-19-1 C₆H₁₆N₂*C₉₅H₆₄N₈O₄Zn₂ 
• 1146196-18-0 C₅H₁₄N₂*C₉₅H₆₄N₈O₄Zn₂ 
• 1146196-21-5 C₇H₁₈N₂*C₉₅H₆₄N₈O₄Zn₂ 
• 1146196-24-8 C₈H₂₀N₂*C₉₅H₆₄N₈O₄Zn₂ 
• 1146196-27-1 C₉H₂₂N₂*C₉₅H₆₄N₈O₄Zn₂ 
• 1146196-13-5 C₂H₈N₂*C₉₅H₆₄N₈O₄Zn₂ 
• 352285-21-3 C₃H₁₀N₂*C₉₅H₆₄N₈O₄Zn₂ 
• 1146196-16-8 C₄H₁₂N₂*C₉₅H₆₄N₈O₄Zn₂ 

Relevant articles and documents

Zinc porphyrin tweezer in host-guest complexation: Determination of absolute configurations of diamines, amino acids, and amino alcohols by circular dichroism

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Dye-sensitizer effects on a Pt/KTa(Zr)O3 catalyst for the photocatalytic splitting of water

(Figure Presented) Back to the elements: The activity of Pt/K 0.95Ta0.92Zr0.08O3 for the photocatalytic splitting of water into H2 and O2 is greatly improved by dye sensitization (see picture). Among the organic dyes examined, the highest photocatalytic activity is obtained with cyanocobalamin (vitamin B12) as a sensitizer.