929115-75-3

Upstream product

• 90-33-5 7-hydroxy-4-methyl-chromen-2-one 
• 92-87-5 p,p'-diaminobiphenyl 
• 108-46-3 recorcinol 

Downstream Products

• 929115-78-6 7-hydroxy-1-{4'-[(4-hydroxy-benzylidene)-amino]-biphenyl-4-yl}-4-methyl-1H-quinolin-2-one 
• 929115-79-7 7-hydroxy-1-{4'-[(4-hydroxy-3-methoxy-benzylidene)-amino]-biphenyl-4-yl}-4-methyl-1H-quinolin-2-one 
• 929115-77-5 7-hydroxy-1-{4'-[(2-hydroxy-benzylidene)-amino]-biphenyl-4-yl}-4-methyl-1H-quinolin-2-one 
• 1321484-75-6 C₃₀H₂₄N₂O₃ 
• 1321484-73-4 C₃₂H₂₈N₂O₅ 
• 1321484-68-7 C₂₉H₂₁N₃O₄ 
• 1321484-76-7 C₂₉H₂₁N₃O₄ 
• 1321484-93-8 C₃₁H₂₃ClN₂O₄ 
• 1321484-92-7 C₃₁H₂₂ClN₃O₅ 
• 1321484-91-6 C₃₁H₂₃ClN₂O₄ 
• 1321484-88-1 C₃₂H₂₅ClN₂O₄ 
• 1321484-86-9 C₃₄H₂₉ClN₂O₆ 
• 1321484-84-7 C₃₃H₂₈ClN₃O₃ 
• 1321484-83-6 C₃₁H₂₂ClN₃O₅ 

Relevant academic research and scientific papers

Microwave assisted synthesis of n-substituted-7-hydroxy-4-methyl-2- oxoquinolines as anticonvulsant agents

The reaction of resorcinol with ethylacetoacetate yielded the 7-hydroxy- 4-methyl coumarin (1), which on treatment with benzidine gives 1-(4'-aminobiphenyl- 4-yl)-7-hydroxy-4-methyl-1H-quinolin-2-one (2). 1-{4'-[(Substituted benzylidene)-amino]-biphenyl-4

Synthesis, characterization and in vitro anti-JEV activity of N-[p-{3′-(2′-aryl-4′-oxo-1′,3′-thiazolyl)} diphenyl]-7-hydroxy-4-methyl-2-oxoquinolines

The synthesis of N-[p-{3′-(2′-aryl-4′-oxo-1′, 3′-thiazolyl)}diphenyl]-7-hydroxy-4-methyl-2-oxoquinolines 4 have been achieved starting from resorcinol. 7-hydroxy-4-methylcoumarin(4- methylumbelliferone) 1 is obtained by the reaction of resorcinol with eth