81820-19-1

Upstream product

• 100-52-7 benzaldehyde 
• 842-74-0 4-benzylidene-2-phenyloxazole-5(4H)-one 
• 150-13-0 4-amino-benzoic acid 

Downstream Products

• 81820-30-6 4-{5-Oxo-2-phenyl-4-[1-phenyl-meth-(Z)-ylidene]-4,5-dihydro-imidazol-1-yl}-N-pyridin-3-yl-benzamide 
• 81820-26-0 N-Butyl-4-{5-oxo-2-phenyl-4-[1-phenyl-meth-(Z)-ylidene]-4,5-dihydro-imidazol-1-yl}-benzamide 
• 81820-27-1 N,N-Diethyl-4-{5-oxo-2-phenyl-4-[1-phenyl-meth-(Z)-ylidene]-4,5-dihydro-imidazol-1-yl}-benzamide 
• 81820-29-3 3-[4-(Morpholine-4-carbonyl)-phenyl]-2-phenyl-5-[1-phenyl-meth-(Z)-ylidene]-3,5-dihydro-imidazol-4-one 
• 81820-28-2 2-Phenyl-5-[1-phenyl-meth-(Z)-ylidene]-3-[4-(piperidine-1-carbonyl)-phenyl]-3,5-dihydro-imidazol-4-one 

Relevant academic research and scientific papers

Synthesis and evaluation of substituted imidazolones for antiinflammatory and antioxidant activities

A series of 4-substituted benzylidene-2-phenyl-1-substituted phenyl-1H-imidazol-5(4H)-one were synthesized by condensation of substituted oxazolones with p-amino benzoic acid and benzocaine. The chemical structures of synthesized compounds were confirmed

2-Phenyl-4-arylidene-2-imidazolin-5-ones and Their Derivatives

A new series of esters and amides (III - VIII) of 1-(p-carboxyphenyl)-2-phenyl-4-arylidene-2-imidazolin-5-ones (IIa - c) have been obtained.Condensation of 2-phenyl-4-arylidene-2-oxazolin-5-ones (I) with sulphonamides gives the corresponding 1-(p-sulphona