103575-50-4

Upstream product

• 4946-14-9 4-mercapto-cumene 
• 75-05-8 acetonitrile 

Downstream Products

• 1383563-66-3 [3-(4-isopropylbenzenesulfonyl)thieno[2,3-e][1,2,3]triazolo-[1,5-a]pyrimidin-5-yl]naphthalen-1-ylmethylamine 
• 892739-49-0 [3-(4-isopropylbenzenesulfonyl)thieno[2,3-e][1,2,3]triazolo-[1,5-a]pyrimidin-5-yl]-(4-methoxybenzyl)amine 
• 892738-96-4 furan-2-ylmethyl-[3-(4-isopropylbenzenesulfonyl)thieno[2,3-e][1,2,3]triazolo[1,5-a]pyrimidin-5-yl]amine 
• 892740-48-6 [3-(4-isopropylbenzenesulfonyl)thieno[2,3-e][1,2,3]triazolo-[1,5-a]pyrimidin-5-yl]thiophen-2-ylmethylamine 
• 1174392-26-7 3-(4-isopropylbenzenesulfonyl)-4H-thieno[2,3-e][1,2,3]-triazolo[1,5-a]pyrimidin-5-one 
• 207853-59-6 (4-isopropylbenzenesulfonyl)-acetonitrile 

Relevant academic research and scientific papers

Cs2CO3-promoted carbon–sulfur bond construction via cross dehydrogenative coupling of thiophenols with acetonitrile

A novel protocol for the construction of carbon–sulfur bonds has been achieved via halogen-free Cs2CO3-promoted cross dehydrogenative coupling (CDC) of thiophenols with acetonitrile. This transformation provides a straightforward route to the synthesis of sulfenylated acetonitriles in up to 80% yield.