62991-69-9

Upstream product

• 74282-74-9 N,N'-Bis(3,5-di-tert-butylphenyl)-N,N'-bis<(4-chlorophenyl)thio>hydrazine 
• 2380-36-1 3,5-di-tert-butylaniline 
• 933-01-7 4-chloro-benzenesulfenyl chloride 
• 74282-61-4 N-(3,5-Di-tert-butylphenyl)-4-chlorobenzenesulfenamide 

Downstream Products

• 74282-74-9 N,N'-Bis(3,5-di-tert-butylphenyl)-N,N'-bis<(4-chlorophenyl)thio>hydrazine 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 80595-94-4 1,3,5,7-tetra-t-butylphenazine 
• 74282-61-4 N-(3,5-Di-tert-butylphenyl)-4-chlorobenzenesulfenamide 
• 80585-16-6 N,N-bis(4-chlorophenylthio)-3,5-di-t-butylaniline 
• 80585-18-8 C₄₀H₅₀Cl₂N₂S₂ 

Relevant academic research and scientific papers

Reaction of a thioaminyl diradical with 7,7,8,8-Tetracyanoquinodimethane (TCNQ). The formation of a cyclophane compound

The reactions of thioaminyl mono- (MONOR) and diradicals (DIR) with 7,7,8,8-tetracyanoquinodimethane (TCNQ) have been investigated. The reactions of TCNQ with MONOR gave 1:2 adducts of TCNQ and MONOR in 85--88% yields, while the reaction with DIR afforded

ESR Study of Persistent Thioaminyls, N-(Arylthio)-3,5-di-tert-butylphenylaminyls

N-(Arylthio)-3,5-di-tert-butylphenylaminyls (2) are generated by hydrogen-abstraction from N-(3,5-di-tert-butylphenyl)arenesulfenamides (1) and are investigated by means of ESR spectroscopy.When the sulfenamides were treated with lead dioxide in benzene,