80595-94-4

Upstream product

• 62991-69-9 N-(4-Chlorophenylthio)-3,5-di-tert-butylphenylaminyl 
• 74282-74-9 N,N'-Bis(3,5-di-tert-butylphenyl)-N,N'-bis<(4-chlorophenyl)thio>hydrazine 
• 128729-17-9 N-(4-Chlorophenylsulfinyl)-3,5-di-t-butylaniline 
• 128729-18-0 N-Methylsulfinyl-3,5-di-t-butylaniline 

Relevant academic research and scientific papers

Persistent Nitrogen-centered Free Radicals, N-(Arylthio)-3,5-di-t-butylphenylaminyls. Decomposition Reactions

N-(4-Chlorophenylthio)-3,5-di-t-butylphenylaminyl was decomposed in oxygen-free benzene, and the products were examined.On the basis of the results, the decomposition mechanism of the radical is described.

Electron Spin Resonance Spectra of Sulfinamidyl Radicals and a Comparison of Hyperfine Splitting Constants with Sulfenamidyl and Sulfonamidyl Radicals

An ESR spectroscopic study of N-arylsulfinyl- and N-alkylsulfinyl-3,5-di-t-butylphenylaminyls (2) is described.The sulfinamidyls 2, generated by the reaction of the corresponding sulfinamides (7) with di-t-butyl diperoxyoxalate (DBPO) in benzene at 21 or