79851-77-7

Upstream product

• 51009-66-6 5-(4-methylbenzylidene)-2-thioxoimidazolidin-4-one 
• 74-88-4 methyl iodide 
• 97693-05-5 5-p-Methylbenzylidene-2-methylmercaptohydantoin 
• 104-87-0 4-methyl-benzaldehyde 
• 79851-69-7 3-Methyl-2-thioxo-5-[1-p-tolyl-meth-(E)-ylidene]-imidazolidin-4-one 

Downstream Products

• 79851-70-0 3-Methyl-2-selenoxo-5-[1-p-tolyl-meth-(E)-ylidene]-imidazolidin-4-one 
• 97693-04-4 3-Methyl-2-[(E)-phenylimino]-5-[1-p-tolyl-meth-(Z)-ylidene]-imidazolidin-4-one 
• 79851-78-8 3-Methyl-2-methylselanyl-5-[1-p-tolyl-meth-(E)-ylidene]-3,5-dihydro-imidazol-4-one 

Relevant academic research and scientific papers

Studies on 5-Arylidene-3-phenyl-2-methylmercaptohydantoins

The action of ammonium acetate on 5-arylidene-3-phenyl-2-methylmercaptohydantoins 1g,h in acetic acid led to the formation of the 5-arylidene-3-phenylhydantoin derivatives 4a,b.In absence of a solvent, ring opening and rearrangement took place with the fo

INTRODUCTION OF SELENIUM TO HETEROCYCLIC COMPOUNDS. PART II. SYNTHESIS OF 3-ALKYL-2-SELENOHYDANTOINS, 2-SELENOHYDANTOIN-3-ACETIC ACID AND 2-SELENORHODANINES WITH DOUBLE BOND AT C-5

The earlier described method was applied to synthesize so far unknown benzylidene derivatives of 3-methyl-2-selenohydantoin, 2-selenohydantoin-3-acetic acid and 2-selenorhodanine.The structures of these compounds were confirmed by the spectral data.Some p