135766-12-0

Basic information

• Product Name: copper(II) 5,10,15,20-tetraphenyl tetrabenzoporphyrinate
• Synonyms: copper(II) 5,10,15,20-tetraphenyl tetrabenzoporphyrinate
• CAS NO: 135766-12-0
• Molecular Weight: 876.519
• Mol File: 135766-12-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: copper(II) 5,10,15,20-tetraphenyl tetrabenzoporphyrinate(CAS DataBase Reference)
• NIST Chemistry Reference: copper(II) 5,10,15,20-tetraphenyl tetrabenzoporphyrinate(135766-12-0)
• EPA Substance Registry System: copper(II) 5,10,15,20-tetraphenyl tetrabenzoporphyrinate(135766-12-0)

Safety Data

• Hazardous Substances Data: 135766-12-0(Hazardous Substances Data)

Upstream product

• 142-71-2 copper diacetate 
• 80529-83-5 cadmium(II) 5,10,15,20-tetraphenyl tetrabenzoporphyrinate 
• 13395-16-9 copper(II) acetylacetonate 

Downstream Products

• 80528-89-8 meso-tetraphenyltetrabenzoporphyrin 

Relevant articles and documents

Copper(II), cobalt(II), cobalt(III), and tin(IV) 5,10,15,20-tetraphenyl tetrabenzoporphyrinates: Synthesis and properties

The complexation reactions of 5,10,15,20-tetraphenyl tetrabenzoporphyrin and the metal exchange reactions of its cadmium(II) complex with copper(II), cobalt(II), and tin(II) acetates and chlorides in a chloroform–methanol mixture and dimethylformamide were studied spectrophotometrically. Corresponding copper(II), cobalt(II), cobalt(II), and tin(IV) porphyrinates were synthesized and identified.

Trans-effect in kinetics of reactions of mixed solvates of Cu(II) acetate with tetraphenyltetrabenzoporphine in organic solvents

The kinetics of complex formation of tetraphenyltetrabenzoporphine with Cu(II) and Zn(II) acetates is studied in individual and mixed coordinating solvents on the basis of DMSO, DMF, and Py. The substantial increase in CuAc2 reactivity in mixed

Effect of a proton-donating solvent on the complexation of classical and nonclassical porphyrins in a pyridine medium

The inhibitory effect of proton-donating additives (HAc) on the rate of coordination reaction (1) of tetrabenzoporphine (H2TBP, I), tetraphenyltetrabenzoporphine (H2TPTBP, II), and N-substituted porphyrins III and IV in pyridine was established. The N-H bonding state in compounds I and II and the reactivity of these compounds in reaction (1) were shown to be similar to those of nonclassical porphyrins (H2P), whereas N-substituted porphyrins apparently do not belong to this group. The inhibition of reaction (1) in the case of compounds III and IV is due to the high basicity of the tertiary nitrogen atoms in these molecules.