87797-55-5

Upstream product

• 87797-40-8 p-t-butylphenyl 3,7-di-t-butyl-1-naphthyl nitroxide 
• 344598-18-1 N-(4-tert-Butyl-phenyl)-N-(3,7-di-tert-butyl-naphthalen-1-yl)-hydroxylamine 
• 20870-33-1 1-bromo-3,7-di-tert-butylnaphthalene 
• 6637-03-2 1-(tert-butyl)-4-nitrosobenzene 
• 87797-48-6 N-p-t-butylphenyl-3,7-di-t-butyl-1,4-naphthoquinone imine 

Relevant academic research and scientific papers

Reactivity and Structure of N-Phenyl-1-naphthylamines and Related Compounds. Part 3. Reaction with Oxygen-centred Radicals

Comparison is made between products obtained by oxidation of N-phenyl-1-naphthylamines and 1-naphthyl phenyl nitroxides with peroxyl radicals.It is concluded that oxidation of the amines does not proceed to a considerable extent via the nitroxides.Comparison is also made of products obtained from these amines and nitroxides by oxidation with Fremy's salt.

Nitroxide Radicals. Part 21. Spontaneous Decomposition of N-Aryl 1- and 2-Naphthyl Nitroxides

N-Aryl 1-naphthyl nitroxides self-react in solution to give the corresponding secondary amines and N-aryl-1,4-naphthoquinone imines.When reaction at the 4-naphthyl position is hindered by substituents benzoquinone imines are also produced.N-Phenyl 2-naphthyl nitroxide under similar conditions gives the corresponding amine and 2-phenylamino-1,4-naphthoquinone via a 1,2-naphthoquinone imine N-oxide intermediate.