1228424-95-0

Basic information

• Product Name: 2-(2-tert-butyl-4,5-dihydroxyphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone
• Synonyms: 2-(2-tert-butyl-4,5-dihydroxyphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone
• CAS NO: 1228424-95-0
• Molecular Weight: 366.46
• Mol File: 1228424-95-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2-tert-butyl-4,5-dihydroxyphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-tert-butyl-4,5-dihydroxyphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone(1228424-95-0)
• EPA Substance Registry System: 2-(2-tert-butyl-4,5-dihydroxyphenyl)-1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethanone(1228424-95-0)

Safety Data

• Hazardous Substances Data: 1228424-95-0(Hazardous Substances Data)

Upstream product

• 98-29-3 4-tert-Butylcatechol 
• 82100-30-9 1-phenyl-2-(tetrahydropyrimidin-2(1H)-ylidene)ethan-1-one 

Relevant articles and documents

Anodic oxidation of catechols in the presence of α-oxoketene N,N-acetals with a tetrahydropyrimidine ring: Selective α-arylation reaction

The electrochemical oxidation of catechols leads to the formation of o-benzoquinones. This property has been applied to effectively synthesize α-arylated products of α-oxoketene N,N-acetals with a tetrahydropyrimidine ring.