7512-49-4

Upstream product

• 55850-14-1 4-phenylamino-naphthalen-1-ol 
• 90-15-3 α-naphthol 
• 586-96-9 Nitrosobenzene 
• 75-91-2 tert.-butylhydroperoxide 
• 90-30-2 N-phenyl-1-naphthylamine 
• 7732-18-5 water 
• 27067-30-7 naphth-1-yl phenyl nitroxide 
• 2834-90-4 4-amino-1-naphthol 
• 344441-80-1 N-1-naphthyl-N-phenylhydroxylamine 
• 90-11-9 1-Bromonaphthalene 

Downstream Products

• 482-89-3 1H,1H'-2,2'-Biindolylidene-3,3'-dione 
• 113689-66-0 4-[(E)-Phenylimino]-2-piperidin-1-yl-4H-naphthalen-1-one 
• 107727-83-3 N,N'-diphenyl-2,2'-bi(1,4-naphthoquinone) 4,4'-diimine 
• 87797-53-3 N-(4-oxonaphthalen-1(4H)-ylidene)aniline oxide 
• 137679-43-7 2-(p-Chlorophenylamino)-N-phenyl-1,4-naphthoquinone monoimine 
• 21720-68-3 2-(phenylamino)-4-(phenylimino)-1(4H)-naphthalenone 
• 106104-40-9 2-(2-Hydroxy-5-methyl-phenylamino)-4-[(E)-phenylimino]-4H-naphthalen-1-one 
• 137679-42-6 2-(p-Bromophenylamino)-N-phenyl-1,4-naphthoquinone monoimine 
• 106087-98-3 2-(2-Hydroxy-5-nitro-phenylamino)-4-[(E)-phenylimino]-4H-naphthalen-1-one 
• 62-53-3 aniline 
• 130-15-4 [1,4]naphthoquinone 
• 71520-42-8 5-hydroxy-13-phenyldibenzocarbazole-7,12-quinone 
• 107727-88-8 5-acetoxy-13-phenyldibenzocarbazole-7,12-quinone 
• 107727-86-6 13-Phenyl-5-phenylamino-13H-13-aza-dibenzo[a,h]fluorene-7,12-dione 

Relevant academic research and scientific papers

Regiodivergent Aromatic Electrophilic Substitution Using Nitrosoarenes in Hexafluoroisopropanol: A Gateway for Diarylamines and p-Iminoquinones Synthesis

A metal-free aromatic electrophilic substitution reaction using nitrosoarenes as the electrophile in 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) is reported. HFIP activates nitrosoarene towards the electrophilic C?H amination followed by a concomitant N?O bo

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.

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.