80883-95-0

Upstream product

• 4392-54-5 4-aminosulfonylphenylhydrazine 
• 959-23-9 4'-methoxychalcone 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 100-52-7 benzaldehyde 
• 17852-52-7 4-hydrazinobenzene-1-sulfonamide hydrochloride 
• 122259-14-7 4-{N'-[(E)-1-(4-Methoxy-phenyl)-3-phenyl-prop-2-en-(E)-ylidene]-hydrazino}-benzenesulfonamide 
• 80883-92-7 4-(3-(4-methoxyphenyl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide 

Downstream Products

• 122259-21-6 4-[4-Bromo-3-(4-methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-benzenesulfonamide 
• 122288-23-7 C₂₆H₂₄N₄O₃S₂ 
• 122259-42-1 C₂₇H₂₈N₄O₄S 
• 122259-45-4 C₂₉H₃₀N₄O₃S₂ 
• 122259-53-4 N-[3-Allyl-4-oxo-thiazolidin-(2E)-ylidene]-4-[3-(4-methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-benzenesulfonamide 
• 122288-24-8 N-[3-Allyl-4-oxo-[1,3]thiazinan-(2E)-ylidene]-4-[3-(4-methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-benzenesulfonamide 
• 122259-54-5 4-[3-(4-Methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-N-[4-oxo-3-phenyl-thiazolidin-(2E)-ylidene]-benzenesulfonamide 
• 122259-55-6 N-[3-Benzyl-4-oxo-thiazolidin-(2E)-ylidene]-4-[3-(4-methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-benzenesulfonamide 
• 122259-59-0 4-[3-(4-Methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-N-[4-oxo-3-phenyl-[1,3]thiazinan-(2E)-ylidene]-benzenesulfonamide 
• 122259-52-3 N-[3-Cyclohexyl-4-oxo-thiazolidin-(2E)-ylidene]-4-[3-(4-methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-benzenesulfonamide 
• 122259-58-9 N-[3-Cyclohexyl-4-oxo-[1,3]thiazinan-(2E)-ylidene]-4-[3-(4-methoxy-phenyl)-5-phenyl-pyrazol-1-yl]-benzenesulfonamide 
• 122288-22-6 C₂₉H₂₄N₄O₄S 
• 122259-41-0 C₂₆H₂₆N₄O₄S 

Relevant academic research and scientific papers

Synthesis, molecular docking study, and cytotoxic activity of 1,3,5-triaryl pyrazole derivatives

Synthesis, molecular docking study, and cytotoxic activity of a new group of 1,3,5-triaryl pyrazole derivatives were be studied. The antiproliferative activity of the final compounds were examined in MCF-7, AGS, HT-29 and NIH3T3 cell lines by MTT assay, u

Pyrazole Derivatives with Possible Hypoglycemic Activity

Condensation of p-sulphamylphenylhydrazine hydrochloride with different chalcones, leads either to hydrzones (2) or to pyrazolines (3) depending on the reaction conditions.The hydrazones (2) are readily converted into pyrazolines (3) on heating with hydro