79070-80-7

Upstream product

• 24815-46-1 N-(phenylthioacetyl)piperidine 

Downstream Products

• 80830-97-3 2-(4-Nitro-phenyl)-4,5-diphenyl-6-piperidin-1-yl-5,6-dihydro-4H-[1,3,4]thiadiazine 
• 75398-45-7 2-p-nitrophenyl-4,5-diphenyl-4H-1,3,4-thiadiazine 
• 83329-90-2 S-1-piperidino-2-phenylethenylthiobenzohydroxamate 
• 80830-92-8 5-piperidino-4-phenyl-3-phenylimino-1,2-dithiole 
• 80830-98-4 [4-(4-Bromo-phenyl)-5-phenyl-6-piperidin-1-yl-5,6-dihydro-4H-[1,3,4]thiadiazin-2-yl]-phenyl-methanone 
• 75398-46-8 2-acetyl-4,5-diphenyl-4H-1,3,4-thiadiazine 
• 80830-96-2 1-(4,5-Diphenyl-6-piperidin-1-yl-5,6-dihydro-4H-[1,3,4]thiadiazin-2-yl)-ethanone 
• 80830-87-1 2,N-Diphenyl-3-piperidin-1-yl-3-thioxo-thiopropionamide 
• 102-08-9 N,N-diphenylthiourea 
• 80830-89-3 2,N-Diphenyl-3-piperidin-1-yl-3-thioxo-propionamide 

Relevant academic research and scientific papers

UNSATURATED THIOLATES AND THEIR ANALOGS IN CYCLOADDITION REACTIONS XI. EFFECT OF SUBSTITUENTS AT THE β POSITION OF ETHENETHIOLATES ON THE DIRECTION OF REACTION WITH CARBON BISULFIDE

1-Dialkylamino-, 1-alkylarylamino-, and 1-cycloalkylaminoethenethiolates react with carbon bisulfide in various directions, depending on the nature of the substituents at the position 2.In all cases 1,2-dithiole-3-thiones are formed.Thiolates unsubstituted at position 2 give, in addition, 5,5'-bis(dialkylamino)-, 5,5'-bis(alkylarylamino)-, and 5,5'-bis(cycloalkylamine)-1,1',2,2'-tetrathiafulvalenes.In the case of potassium 1-morpholino-2-tert-butylethenethiolate the reaction is accompanied by the elimination of a molecule of morpholine and by the formation of 4-tert-butyl-1,2-dithiole-3-thione.In the presence of a weak proton donor (acetonitrile) ethylenethiolates substituted at position 2 react normally, but the 1-piperidinoethenethiolate gives mainly N,N-pentamethylenetrithiomalonamide.