1558083-10-5

Upstream product

• 28081-12-1 3-(4-chlorophenyl)-1-(4-fluorophenyl)prop-2-en-1-one 
• 141-97-9 ethyl acetoacetate 
• 104-88-1 4-chlorobenzaldehyde 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Downstream Products

• 1471413-44-1 4-(4-chlorophenyl)-6-(4-fluorophenyl)-1,2,4,5-tetrahydro-3H-indazol-3-one 
• 1471413-50-9 4-(4-chlorophenyl)-6-(4-fluorophenyl)-2-(4-nitrophenyl)-1,2,4,5-tetrahydro-3H-indazol-3-one 
• 1471413-53-2 4-(4-chlorophenyl)-2-(2,4-dinitrophenyl)-6-(4-fluorophenyl)-1,2,4,5-tetrahydro-3H-indazol-3-one 

Relevant academic research and scientific papers

Synthesis, structure-activity relationship and molecular docking of cyclohexenone based analogous as potent non-nucleoside reverse-transcriptase inhibitors

The chalcones core in compounds is advantageously chosen effective synthons, which offer exciting perspectives in biological and pharmacological research. The present study reports the successful development of eight new cyclohexenone based anti-reverse t

Synthesis of new indazole derivatives as potential antioxidant agents

New indazole derivatives were synthesized by reacting hydrazine hydrate and its derivatives with cyclohexenone derivatives, which in turn prepared from respective chalcones. The chemical structure of newly synthesized compounds was well characterized by using 1H NMR, 13C NMR, IR and mass spectral data. All the synthesized products were screened for their antioxidant properties. All indazole derivatives exhibited noticeable DPPH radical scavenging activity, reducing power capacity and total antioxidant capacity in comparison with the respective standards. Springer Science+Business Media 2013.