24486-68-8

Upstream product

• 98-77-1 piperidinium piperidyldithiocarbamate 
• 19339-59-4 1-(4-chloro-phenyl)-2-thiocyanato-ethanone 

Downstream Products

• 119824-96-3 Piperidine-1-carbodithioic acid 2-(4-chloro-phenyl)-1-[1,3]dithiolan-2-ylidene-2-oxo-ethyl ester 
• 119824-92-9 Piperidine-1-carbodithioic acid 1-(4-chloro-benzoyl)-2,2-bis-methylsulfanyl-vinyl ester 
• 88559-24-4 5-(4-chloro-benzoyl)-4-methylthio-1,3-dithiole-2-thione 
• 119825-00-2 Piperidine-1-carbodithioic acid 2-(4-chloro-phenyl)-1-[1,3]dithian-2-ylidene-2-oxo-ethyl ester 

Relevant academic research and scientific papers

Cyclic ammonium salts of dithiocarbamic acid: stable alternative reagents for the synthesis of S-alkyl carbodithioates from organyl thiocyanates in water

ABSTRACT: Carbodithioate esters are important functional organosulfur compounds widely used in diverse fields such as pharmaceuticals, agrochemicals and material sciences. Common preparative methods include reaction of alkyl halides, carbon disulfide and bases under both metal-free and metal-catalyzed conditions. However, organyl thiocyanates have not been previously explored, possibly because of their conversion to organyl disulfides under basic conditions. Here, we report an efficient and practical method for the preparation of libraries of carbodithioate esters from organyl thiocyanates by reacting with cyclic amine-based dithiocarbamic acid salts in water. The protocol is found to be applicable in general to various thiocyanates such as benzyl/aroyl methyl/cinnamyl and so on. Other notable features include no by-products such as disulfides, metal- and alkali-free, aqueous conditions, and finally easy and near-quantitative formation of cyclic amine-based dithiocarbamic acid salt as a stable alternative reagent.