89316-45-0

Upstream product

• 108-46-3 recorcinol 
• 5614-80-2 ethyl 2-((2-oxo-4-phenyl-2H-chromen-7-yl)oxy)acetate 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 

Downstream Products

• 1092840-42-0 1-[(furan-2-yl)methylene]-2-(2-oxo-4-phenyl-2H-benzo[b]pyran-7-yloxy)acetohydrazide 
• 1092840-43-1 1-[(thiophen-2-yl)methylene]-2-(2-oxo-4-phenyl-2H-benzo[b]pyran-7-yloxy)acetohydrazide 
• 1092840-44-2 1-(4-chlorobenzylidene)-2-(2-oxo-4-phenyl-2H-benzo[b]pyran-7-yloxy)acetohydrazide 
• 89316-60-9 1-(4-nitrobenzylidene)-2-(2-oxo-4-phenyl-2H-benzo[b]pyran-7-yloxy)acetohydrazide 
• 89316-53-0 1-(benzylidene)-2-(2-oxo-4-phenyl-2H-benzo[b]pyran-7-yloxy)acetohydrazide 
• 89316-57-4 1-(4-methoxybenzylidene)-2-(2-oxo-4-phenyl-2H-benzo[b]pyran-7-yloxy)acetohydrazide 

Relevant academic research and scientific papers

New 4-phenylcoumarin derivatives as potent 3C protease inhibitors: Design, synthesis, anti-HAV effect and molecular modeling

A new series of 4-phenylcoumarin derivatives was synthesized starting from (2-oxo-4-phenyl-2H-chromen-7-yloxy) acetic acid hydrazide 3. Evaluation of the target compounds for their antiviral activity against hepatitis A virus revealed that the ethylthiose

Synthesis and biological evaluation of novel 7-hydroxy-4-phenylchromen-2-one–linked to triazole moieties as potent cytotoxic agents

A new series of novel 7-hydroxy-4-phenylchromen-2-one (1a)–linked 1,2,4-triazoles were synthesised using a click chemistry approach. All derivatives were subjected to 3-(4,5-dimethylthiazol-yl)-diphenyl tetrazolium bromide (MTT) cytotoxicity screening aga