4759-28-8

Basic information

• Product Name: tritylphosphonic acid
• Synonyms: tritylphosphonic acid
• CAS NO: 4759-28-8
• Molecular Weight: 324.316
• Mol File: 4759-28-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: tritylphosphonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: tritylphosphonic acid(4759-28-8)
• EPA Substance Registry System: tritylphosphonic acid(4759-28-8)

Safety Data

• Hazardous Substances Data: 4759-28-8(Hazardous Substances Data)

Upstream product

• 596-43-0 bromo-triphenyl-methane 
• 15205-58-0 tricyclohexyl phosphite 
• 3736-70-7 triphenylphosphonyl dichloride 
• 141-52-6 sodium ethanolate 
• 166660-56-6 triphenylmethylphosphinic acid 
• 852692-39-8 trityl-phosphonic acid ethyl ester chloride 
• 108-88-3 toluene 
• 76-84-6 triphenylmethyl alcohol 
• 71-43-2 benzene 
• 124-41-4 sodium methylate 
• 129769-61-5 di-p-tolyl triphenylmethylphosphonate 
• 129769-62-6 bis(4-methoxyphenyl) triphenylmethylphosphonate 
• 7719-12-2 phosphorus trichloride 
• 7732-18-5 water 

Downstream Products

• 102660-13-9 triphenylmethylphosphonic acid dimethyl ester 
• 92-52-4 biphenyl 
• 129769-68-2 α-methoxybenzylphosphonic acid 
• 519-73-3 triphenylmethane 
• 123629-03-8 phosphonic acid 
• 852692-39-8 trityl-phosphonic acid ethyl ester chloride 
• 76-83-5 trityl chloride 

Relevant articles and documents

Structural analogues of bioactive phosphonic acids: First crystal structure characterization of phosphonothioic and boranophosphonic acids

Phosphonothioic and boranophosphonic acids have been structurally characterized for the first time by single X-ray crystallography. These two functional groups, and the corresponding phosphonic acid, were all conveniently synthesized in high yields from t

Photolysis of triarylmethylphosphonic acids and their esters

Upon UV-irradiation in an alkaline alcohol solution, some triarylmethylphosphonic acids underwent C-P bond cleavage to give triarylmethanes and alkyl dihydrogenphosphates, while, in an acidic or a neutral alcohol solution, they afforded biaryls. Their dimethyl esters gave also biaryls and dimethyl [alkoxy(aryl)methyl]phosphonates, which were derived from the insertion of (dialkoxyphosphinyl) arylcarbenes into the OH bond of the alcohol. The carbene was generated by photo-α,α-elimination of two aryl groups of the phosphonate.