10220-34-5

Usage

Uses

Used in Rubber Industry:
N-isopropylbenzothiazol-2-sulphenamide is used as a rubber vulcanization accelerator for its ability to speed up the process of converting rubber compounds into a stronger, more durable material. This application is crucial in the production of rubber and rubber products, ensuring improved quality and performance.
Used in Medical Field (Research):
N-isopropylbenzothiazol-2-sulphenamide has been identified for its potential applications in the medical field, particularly in the treatment of certain types of cancer. Its role in this context is still under investigation, and further research is required to fully understand and harness its potential in cancer therapy.

InChI:InChI=1/C10H12N2S2/c1-7(2)12-14-10-11-8-5-3-4-6-9(8)13-10/h3-7,12H,1-2H3

Upstream product

• 67-56-1 methanol 
• 2801-21-0 benzothiazole sulfenamide 
• 75-31-0 isopropylamine 
• 2492-26-4 sodium 2-mercaptobenzothiazole 
• 60-29-7 diethyl ether 
• 114698-09-8 benzothiazole-2-sulfenyl thiocyanate 
• 40576-88-3 propan-2-one S-benzothiazol-2-yl-thiooxime 
• 149-30-4 2-Mercaptobenzothiazole 
• 149-30-4 2-thioxo-3H-1,3-benzothiazole 
• 120-78-5 di(benzothiazol-2-yl)disulfide 

Downstream Products

• 3741-79-5 bis-benzothiazol-2-ylsulfanyl-isopropyl-amine 
• 2757-92-8 2-(ethylthio)benzothiazole 
• 16407-34-4 3-aethylbenzothiazolin-2-thion 
• 68837-83-2 C₁₉H₃₂N₃OPS₂ 
• 22685-19-4 diethyl N-isopropylphosphoramidate 
• 149-30-4 2-Mercaptobenzothiazole 
• 74124-46-2 diisopropyl N-isopropylphosphoramidate 
• 75291-14-4 Thiophosphoric acid S-benzothiazol-2-yl ester O,O'-diisopropyl ester 
• 615-22-5 2-methylmercaptobenzothiazole 
• 2254-94-6 3-methylbenzothiazole-2-thione 
• 130888-07-2 C₁₁H₁₆N₃OPS₂ 
• 74124-43-9 N-(1-methylethyl)-O,O-dimethylphosphoramidate 
• 68835-08-5 tetraethyl-thiophosphorodiamidic acid S-benzothiazol-2-yl ester 

Relevant academic research and scientific papers

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.

Manufacture of sulfenamides

Processes for the manufacture of sulfenamides by the oxidation of a mixture of 2-mercaptobenzothiazole and the appropriate amine in a critical amount of water and/or organic solvent produces a pure product of good quality and high yield. The amount of water should be in the range of from 10 to 30% by weight based on the total reaction mixture.

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.