20104-42-1

Basic information

• Product Name: [1,1':3',1''-Terphenyl]-2'-ol, 5'-([1,1':3',1''-terphenyl]-2'-yloxy)-
• CAS NO: 20104-42-1
• Molecular Formula: C36H26O2
• Molecular Weight: 490.601
• Mol File: 20104-42-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 639.5±55.0 °C(Predicted)
• Density: 1.169±0.06 g/cm3(Predicted)
• CAS DataBase Reference: [1,1':3',1''-Terphenyl]-2'-ol, 5'-([1,1':3',1''-terphenyl]-2'-yloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1':3',1''-Terphenyl]-2'-ol, 5'-([1,1':3',1''-terphenyl]-2'-yloxy)-(20104-42-1)
• EPA Substance Registry System: [1,1':3',1''-Terphenyl]-2'-ol, 5'-([1,1':3',1''-terphenyl]-2'-yloxy)-(20104-42-1)

Safety Data

• Hazardous Substances Data: 20104-42-1(Hazardous Substances Data)

Upstream product

• 20104-40-9 2,6-diphenylanisole 
• 79650-54-7 2,6-diphenylphenoxide sodium salt 
• 2432-11-3 (1,1';3',1''-terphenyl)-2'-ol 
• 20104-39-6 4-bromo-2,6-diphenylanisole 

Downstream Products

• 79650-52-5 2,6-Diphenyl-4-<2,6-diphenyl-phenoxyl-Radikal 

Relevant articles and documents

Flash Photolysis Study of Phenyl-substituted Phenols, Quinones, and Corresponding Free Radicals. Part 3. Intermediates in the Photolysis of Phenyl-substituted Phenols

Aryloxyl radicals are formed on photoexcitation of phenyl-substituted phenols in a biphotonic process involving the triplet excited state.These aryloxyl radicals are also formed on photolysis of the corresponding phenolate ions in the presence of oxygen i