74282-61-4

Upstream product

• 62991-69-9 N-(4-Chlorophenylthio)-3,5-di-tert-butylphenylaminyl 
• 933-01-7 4-chloro-benzenesulfenyl chloride 
• 2380-36-1 3,5-di-tert-butylaniline 
• 100-42-5 styrene 
• 74282-74-9 N,N'-Bis(3,5-di-tert-butylphenyl)-N,N'-bis<(4-chlorophenyl)thio>hydrazine 
• 106-44-5 p-cresol 
• 95-48-7 ortho-cresol 
• 576-26-1 2.6-dimethylphenol 

Downstream Products

• 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 

Relevant academic research and scientific papers

PERSISTENT NITROGEN-CENTERED FREE RADICALS, N-(ARYLTHIO)-3,5-DI-t-BUTYLPHENYLAMINYLS. THE REACTIONS WITH PHENOLS.

In order to examine the properties of a new class of nitrogen-centered free radicals, reactions of N-(4-chlorophenylthio)-3,5-di-t-butylphenylaminyl were carried out with a variety of phenols. Results are reported.

Efficient Additions of an Electronically Stabilized Persistent Aminyl Radical to Conjugated Alkenes

It has been found that an electronically stabilized persistent N-(4-chlorophenylthio)-3,5-di-t-butyl-phenylaminyl radical (1) adds to conjugated alkenes to afford 1:2 adducts of the alkenes and 1 in fair to excellent yields, along with small amounts of 1:

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.

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,