107125-57-5

Basic information

• Product Name: 3-bromo-4-(2,4-dibromophenyl)imino-1,4-benzoquinone
• Synonyms: 3-bromo-4-(2,4-dibromophenyl)imino-1,4-benzoquinone
• CAS NO: 107125-57-5
• Molecular Weight: 419.898
• Mol File: 107125-57-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-bromo-4-(2,4-dibromophenyl)imino-1,4-benzoquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-4-(2,4-dibromophenyl)imino-1,4-benzoquinone(107125-57-5)
• EPA Substance Registry System: 3-bromo-4-(2,4-dibromophenyl)imino-1,4-benzoquinone(107125-57-5)

Safety Data

• Hazardous Substances Data: 107125-57-5(Hazardous Substances Data)

Upstream product

• 154928-50-4 3-bromo-4-(2,4-dibromo-anilino)-phenol 
• 122-37-2 4-anilinophenol 
• 2406-04-4 4-(phenylimino)cyclohexa-2,5-dienone 
• 154928-51-5 3-bromo-4-phenylimino-1,4-benzoquinone 
• 68141-98-0 N-(4-Bromophenyl)-1,4-benzoquinone monoimine 

Downstream Products

• 3958-82-5 2-bromo-1,4-benzoquinone 
• 615-57-6 2,4-dibromo-aniline 

Relevant articles and documents

REACTION OF HYDROGEN BROMIDE WITH N-ARYL-1,4-BENZOQUINONE MONOIMINES

Bromine enters the position ortho to nitrogen on nucleophilic addition of hydrogen bromide to N-phenyl-1,4-benzoquinone monoimine.Bromination of the aryl nucleus is a parallel process, which may be suppressed by adding resorcinol to the reaction mixture.Bromine enters the position ortho to oxygen in the reaction of HBr and N-(2,4-dinitrophenyl)-1,4-benzoquinone monoimine.A dependence of the reactivity on the redox potential of the quinone imine was noted.