50931-28-7

Upstream product

• 91-20-3 naphthalene 
• 127-65-1 chloroamine-T 
• 98-59-9 p-toluenesulfonyl chloride 
• 155338-66-2 N,N-ditosyl-4-nitronaphthylamine 
• 36942-36-6 4-methyl-N-(4-nitronaphthalen-1-yl)benzenesulfonamide 
• 155338-69-5 N-tosyl-1,4-naphthalenediamine 
• 776-34-1 1-amino-4-nitronaphthalene 
• 155338-73-1 N,N′-(naphthalene-1,4-diyl)bis(4-methylbenzenesulfonamide) 

Downstream Products

• 50931-31-2 Diisopropyl <4-(p-toluenesulfonamido)-1-naphthyl>(p-tolylsulfonyl)phosphoramidate 

Relevant academic research and scientific papers

SYNTHESIS OF UNSYMMETRICAL 1,4-NAPHTHOQUINONE DIIMIDES

The reaction of 4-nitronaphthylamine with methane-, benzene-, and p-toluenesulfonyl chlorides in pyridine gave N,N-diacyl-4-nitronaphthylamines, which were converted by alkaline hydrolysis into N-acyl-4-nitronaphthylamines.With benzoyl chloride the reacti

Functionalisation of Saturated Hydrocarbons. Part 1. Some Reactions of a Ferrous Chloride-Chloramine-T Complex with Hydrocarbons

The reactions of several hydrocarbons substrates with a ferrous chloride-chloramine-T complex, generated in situ, have been studied.Tosylamination of adamantane and chlorination of mesitylene proceed in good yield while naphthalene gives N,N'-bis(toluene-p-sulphonyl)-1,4-naphthoquinone di-imine.A variety of olefinic substrates undergo both cis- and trans-addition to the double bond as well as allylic functionalisation.