32730-01-1

Upstream product

• 100-52-7 benzaldehyde 
• 4303-27-9 2,4-dithioxothiazolidine 
• 3806-42-6 5-benzylidene-2-thioxothiazolidin-4-one 

Downstream Products

• 73833-53-1 1-((5S,6R,7R)-5,7-Diphenyl-2-thioxo-3,5,6,7-tetrahydro-2H-thiopyrano[2,3-d]thiazol-6-yl)-ethanone 
• 73833-53-1 1-((5R,6S,7R)-5,7-Diphenyl-2-thioxo-3,5,6,7-tetrahydro-2H-thiopyrano[2,3-d]thiazol-6-yl)-ethanone 
• 73833-44-0 6-Methyl-7-phenyl-2-thioxo-3,5,6,7-tetrahydro-2H-thiopyrano[2,3-d]thiazole-6-carboxylic acid methyl ester 
• 57391-32-9 (5R,6S,7S)-6-Nitro-5,7-diphenyl-3,5,6,7-tetrahydro-thiopyrano[2,3-d]thiazole-2-thione 
• 57391-32-9 (5S,6R,7S)-6-Nitro-5,7-diphenyl-3,5,6,7-tetrahydro-thiopyrano[2,3-d]thiazole-2-thione 

Relevant academic research and scientific papers

Uses of 2-(thiophene-2-carbonylcarbamothioylthio)acetic acid as a good synthon for construction of some new thiazole and annulated thiazole derivatives

The reaction of thiophene-2-carbonyl isothiocyanate 2 with thioglycolic acid gave 2-(thiophene-2-carbonylcarbamothioylthio) acetic acid 3. Compound 3 was subjected to some selected reactions with sulphuric acid as well as benzaldehyde, piperonal and isati

A simple green synthesis of (Z)-5-arylmethylene-4-thioxothiazolidines and thiopyrano[2,3-d]thiazolidine-2-thiones in PEG-400 under catalyst-free conditions

An improved Knoevenagel condensation of various aromatic aldehydes with thiazolidine-2,4-dithione and with 4-thioxothiazolidin-4-one can be achieved at room temperature in polyethylene glycol-400 without catalyst to afford (Z)-5-arylmethylene-4-thioxothia