32997-27-6

Upstream product

• 2492-26-4 sodium 2-mercaptobenzothiazole 
• 109-73-9 N-butylamine 
• 2801-21-0 benzothiazole sulfenamide 
• 149-30-4 2-Mercaptobenzothiazole 

Downstream Products

• 120-78-5 di(benzothiazol-2-yl)disulfide 
• 109-73-9 N-butylamine 
• 615-22-5 2-methylmercaptobenzothiazole 
• 20465-01-4 N-butyl-O,O-dimethylphosphoramidate 

Relevant academic research and scientific papers

The aqueous phase is generated in the catalytic molecular oxygen with S - N key of the sulfenamide compounds (by machine translation)

The invention provides a water-phase catalytic molecular oxygen generation has S - N key of the sulfenamide compounds, in order to water-soluble transition metal phthalocyanine compound as a catalyst, in oxygen or in the air environment, the mercapto comp

ON THE REACTION OF BENZOTHIAZOL-2-YL SULPHENAMIDES WITH PHOSPHITES

A study of the synthesis of phosphoramidates from phosphites and benzothiazol-2-yl-sulphenamides, indicates that a quinquecovalent phosphorane is an intermediate.Since the initial step in this reaction does not involve attack of phosphorus on nitrogen, it is unlikely that these sulphenamides will act as electrophilic aminating agents towards non-phosphorus nucleophiles.An efficient new method for preparing benzothiazol-2-yl-sulphenamides is reported.

Process for the preparation of thiazolesulphenamides

Thiazolesulphenamides, useful as rubber vulcanization accelerators, are made by reaction of a 2-mercapto-thiazole or a 2,2'-dithiazolyl disulphide with ammonia or a primary or secondary amine in the presence of oxygen and a copper catalyst of specified kind.