124554-09-2

Basic information

• Product Name: 4-p-toluidino-[1,2]naphthoquinone-1-p-tolylimine
• Synonyms: 4-p-toluidino-[1,2]naphthoquinone-1-p-tolylimine
• CAS NO: 124554-09-2
• Molecular Weight: 352.436
• Mol File: 124554-09-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-p-toluidino-[1,2]naphthoquinone-1-p-tolylimine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-p-toluidino-[1,2]naphthoquinone-1-p-tolylimine(124554-09-2)
• EPA Substance Registry System: 4-p-toluidino-[1,2]naphthoquinone-1-p-tolylimine(124554-09-2)

Safety Data

• Hazardous Substances Data: 124554-09-2(Hazardous Substances Data)

Upstream product

• 131-91-9 1-Nitroso-2-naphthol 
• 550-60-7 1-nitro-2-naphthol 
• 3560-30-3 1-(phenylamino)naphthalen-2-ol 
• 106-49-0 p-toluidine 
• 104732-13-0 o-naphthoquinone monoanil 
• 67-64-1 acetone 

Downstream Products

• 69085-39-8 4-((4-methylphenyl)amino)naphthalene-1,2-dione 

Relevant articles and documents

Aryliminodimagnesium Reagents. XVI. Formation of o-Hydroxyazoarenes by Condensation with o-Hydroxynitroarenes. Favorable Role of o-Hydroxyl Group in the Reaction

Hydroxy(HO)-azoxy and -azoarenes were formed by condensation of ArN(MgBr)2 with o-, m-, and p-HO-nitrobenzenes; nuclear substitution took place as a minor or a major pathway. o-HO-azobenzene was obtained in sufficiently high yield.Relative yields of the products varied according to the position of HO group and reaction conditions.The yield variation was explained by the effects of relative efficiency of single electron transfer, ?-complexation, and cooperation of reagent molecules.