1131-29-9

Upstream product

• 78375-81-2 N-aniline 
• 1127-42-0 N-tert-butyl-N-phenylhydroxylamine 
• 23819-68-3 N-t-butyl-N-(p-formylphenyl)hydroxylamine 
• 78375-79-8 N-t-butyl-N-(p-methoxymethylphenyl)hydroxylamine 
• 96259-22-2 4-methoxymethylphenylmagnesium bromide 

Downstream Products

• 19617-94-8 2,5-bis(t-butylamino)-p-benzoquinone 
• 106-51-4 p-benzoquinone 
• 83933-71-5 2-(2,2,4,4-tetramethylpyrrolidin-1-yl)-p-benzoquinone 
• 25295-92-5 2,5-bis(1,1,3,3-tetramethylbutylamino)-p-benzoquinone 
• 1520-99-6 2,5-bis(butylamino)-1,4-benzoquinone 

Relevant academic research and scientific papers

Alkyl Nitrenes from N-Alkylbenzoquinone Imine N-Oxides

Alkyl nitrenes have been generated by photolysis of two N-t-alkylbenzoquinone imine N-oxides.These mainly abstract hydrogen to give the corresponding amines which are trapped by reaction with benzoquinone.Intramolecular hydrogen abstraction followed by cyclisation to give a pyrrolidine is a minor process in one case.Attempts to generate α-substituted benzyl nitrenes in this way led mainly to the production of substituted benzyl radicals by C-N bond cleavage of the N-benzylbenzoquinone imine N-oxides.

Nitroxide Radicals. Part 20. Formation and Reactions of t-Butyl p-Formylphenyl Nitroxide and its Derivatives

Preparation of the parent hydroxylamine of the title nitroxide and its conversion into several hydroxylamine derivatives and the corresponding nitroxides has been achieved with a view to using functionalised aryl nitroxides as spin labels.The aN/sub