200804-80-4

Upstream product

• 1121-60-4 pyridine-2-carbaldehyde 
• 2010-15-3 3-phenyl-2-thioxoimidazolidin-4-one 

Downstream Products

• 1224692-33-4 (5Z)-5-(pyridin-2-ylmethylidene)-3-phenyl-2-(carbethoxymethylthio)-4,5-dihydro-4H-imidazol-4-one 
• 804499-67-0 2-methylthio-5-(2-pyridyl)methylene-3-phenyl-3,5-dihydro-4H-imidazol-4-one 
• 922726-82-7 Cu((5Z)-2-methylthio-3-phenyl-5-(α-pyridylmethylidene)-3,5-dihydro-4H-imidazol-4-one)Cl2 
• 1438192-36-9 methyl 2-[[(4Z)-5-oxo-1-phenyl-4-(2-pyridylmethylene)-4,5-dihydro-1H-imidazol-2-yl]thio]-propionate 
• 1438192-39-2 methyl 2-[[(4Z)-5-oxo-1-phenyl-4-(2-pyridylmethylene)-4,5-dihydro-1H-imidazol-2-yl]thio]-butanoate 
• 1438192-42-7 ethyl 3-[[(4Z)-5-oxo-1-phenyl-4-(2-pyridylmethylene)-4,5-dihydro-1H-imidazol-2-yl]thio]-propanoate 
• 1438192-45-0 ethyl 3-[[(4Z)-5-oxo-1-phenyl-4-(2-pyridylmethylene)-4,5-dihydro-1H-imidazol-2-yl]thio]-propanoate 

Relevant academic research and scientific papers

Coordination compounds of s-and se-containing organic ligands as catalysts of oxidation reaction under N 2O action

Nitrous oxide (N2O) would be preferable to many other oxidants because in the reactions of N2O with organic compounds the only byproduct is N2, which is perfect from the point of view of green chemistry. We recently reported a series of new sulfur-and sel

A convenient synthesis of glycosylated hydantoins as potential antiviral agents

Reaction of 5-arylidene-2-thiohydantoins 3a-d with glycosyl halides 4a,b under alkaline conditions gave the respective bisglycosylated derivatives 5a-h. Deacetylation with ammonia in methanol caused a change of the S-glycosyl residue and gave the N-3 glyc

Study of 5-arylidene-2-thiohydantoins with potential immunomodulating and anticancer activities

Various 5-arylidene-2-thiohydantoins, N3-substituted and/or S-substituted or not, were synthesized by aldolisation-crotonisation reaction from aromatic aldehydes or cyclic ketones and 2-thiohydantoins. These products, largely original, prepared as potenti