33053-06-4

Basic information

• Product Name: 3,5-Pyrazolidinedione, 4-butyl-4-hydroperoxy-1,2-diphenyl-
• CAS NO: 33053-06-4
• Molecular Formula: C19H20N2O4
• Molecular Weight: 340.379
• Mol File: 33053-06-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,5-Pyrazolidinedione, 4-butyl-4-hydroperoxy-1,2-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Pyrazolidinedione, 4-butyl-4-hydroperoxy-1,2-diphenyl-(33053-06-4)
• EPA Substance Registry System: 3,5-Pyrazolidinedione, 4-butyl-4-hydroperoxy-1,2-diphenyl-(33053-06-4)

Safety Data

• Hazardous Substances Data: 33053-06-4(Hazardous Substances Data)

Upstream product

• 50-33-9 Phenylbutazone 

Downstream Products

• 16860-42-7 2-carboxy-2-hydroxycapronsaure-N,N'-diphenylhydrazid 
• 16860-43-8 4-Butyl-4-hydroxy-1,2-diphenyl-1H-pyrazol-3,5(2H,4H)-dion 

Relevant articles and documents

A dinuclear palladium catalyst for α-Hydroxylation of carbonyls with O2

A chemo- and regioselective α-hydroxylation reaction of carbonyl compounds with molecular oxygen as oxidant is reported. The hydroxylation reaction is catalyzed by a dinuclear Pd(II) complex, which functions as an oxygen transfer catalyst, reminiscent of an oxygenase. The development of this oxidation reaction was inspired by discovery and mechanism evaluation of previously unknown Pd(III)-Pd(III) complexes.

Chemical synthesis of phenylbutazone hydroperoxide and investigation of the drug for cardiac action under in vitro and in vivo conditions

Phenylbutazone (4-n-butyl-1,2-diphenyl-pyrazolidine-3,5-dione) 1 is an easily autoxidable substance which forms a crystalline and stable hydroperoxide 3. The decomposition of 3 yields products which were investigated as metabolites of the drug. In isolate