76579-52-7

Usage

InChI:InChI=1/C11H15NOS/c1-12(2)11(14)8-9-4-6-10(13-3)7-5-9/h4-7H,8H2,1-3H3

Upstream product

• 124-40-3 dimethyl amine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 4137-10-4 DIMCARB 
• 35453-06-6 4-methoxy-β-methylsulfinyl-β-methylthiostyrene 
• 104-47-2 p-methoxybenzylnitrile 
• 68-12-2 N,N-dimethyl-formamide 
• 830-09-1 3-(4'-methoxyphenyl)propenoic acid 

Downstream Products

• 131801-70-2 N,N-dimethyl-α-(1-hydroxycyclohexyl)-p-methoxyphenylthioacetamide 
• 539-15-1 N,N-dimethyltyramine 
• 104-01-8 4-Methoxyphenylacetic acid 
• 124-40-3 dimethyl amine 
• 775-33-7 4-methoxyphenethyl-dimethylamine 

Relevant academic research and scientific papers

Sulfur promoted decarboxylative thioamidation of carboxylic acids using formamides as amine proxy

An efficient decarboxylative thioamidation of arylacetic and cinnamic acids has been developed employing formamides as amine surrogate and sulfur as promoter. Thioamides with variant structural features are obtained under mild reaction conditions without the use of transition metal catalysts and oxidants.

Copper(II)-catalyzed reactions of dimethylformamide with phenylacetonitrile and sulfur to form N,N-dimethylthioamides

Novel copper-catalyzed three-component reactions of phenylacetonitrile, sulfur and DMF (dimethyformamide) for the selective preparation of N,N-dimethylthiobenzamide and N,N-dimethyl-2-phenylethanethioamides in yields of up to 96% are described. Copyright

Dimethylammonium Dimethylcarbamate - A Useful Reagent for the Willgerodt-Kindler Reaction

Dimethylammonium dimethylcarbamate (dimcarb), easily accessible from dimethylamine and carbon dioxide, is a useful reagent for the Willgerodt-Kindler synthesis of N,N-dimethylthiocarboxamides.Moreover, dimcarb displays some unusual properties, and generally behaves as a preparatively useful dimethylamine source.