358656-98-1

Upstream product

• 591-31-1 3-methoxy-benzaldehyde 
• 100-19-6 (4-nitrophenyl)ethanone 

Downstream Products

• 1427302-11-1 (Z)-2-azido-3-(3-methoxyphenyl)-1-(4-nitrophenyl)prop-2-en-1-one 
• 1427302-32-6 1-(5-(3-methoxyphenyl)-2-methyl-4-(4-nitrobenzoyl)-1H-pyrrol-3-yl)ethanone 
• 1427302-45-1 2,2,2-trifluoro-1-(5-(3-methoxyphenyl)-2-methyl-4-(4-nitrobenzoyl)-1H-pyrrol-3-yl)ethanone 
• 1427302-49-5 (4-benzoyl-2-(3-methoxyphenyl)-5-phenyl-1H-pyrrol-3-yl)(4-nitrophenyl)methanone 
• 1416989-37-1 6-(3-methoxyphenyl)-4-(4-nitrophenyl)-5,6-dihydropyrimidin-2(1H)-thione 
• 1416989-27-9 6-(3-methoxyphenyl)-4-(4-nitrophenyl)-5,6-dihydropyrimidin-2(1H)-one 
• 1416989-47-3 5-(3-methoxyphenyl)-3-(4-nitrophenyl)-4,5-dihydroisoxazole 
• 1416989-20-2 5-(3-methoxyphenyl)-3-(4-nitrophenyl)-4,5-dihydro-1H-pyrazole 

Relevant academic research and scientific papers

Synthesis, antitubercular activity, and QSAR analysis of substituted nitroaryl analogs: Chalcone, pyrazole, isoxazole, and pyrimidines

In the present investigation, 4-nitroacetophenone, on condensation with appropriate aldehydes in ethanolic sodium hydroxide solution, yielded the corresponding chalcones. These corresponding chalcones were reacted with hydrazine hydrate, urea, thiourea, a

Interactive free energy relationships for non-additive multiple substituent effects in base catalysed condensation of benzaldehydes with acetophenones: A kinetic study

The base-catalysed condensation of benzaldehydes with acetophenones is enhanced by electron-withdrawing substituents in both starting compounds.The magnitude of ρ-value obtained for various substituents in the benzaldehyde moiety decreases with the introduction of electron-withdrawing groups in the para position of acetophenone moiety.