57366-48-0

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 109-77-3 malononitrile 
• 49629-37-0 2-(4-methoxybenzylidene)-1-tetralone 
• 105-56-6 ethyl 2-cyanoacetate 

Downstream Products

• 1393730-87-4 C₂₂H₁₆N₂O₃ 
• 66128-47-0 4-(4-methoxy-phenyl)-1-methyl-2-oxo-1,2,5,6-tetrahydro-benzo[h]quinoline-3-carbonitrile 
• 1393731-17-3 C₂₃H₂₀N₂O₂ 
• 57366-59-3 1-Acetyl-4-(4-methoxy-phenyl)-2-oxo-1,2,5,6-tetrahydro-benzo[h]quinoline-3-carbonitrile 
• 1393730-99-8 C₂₈H₂₁N₃O₂S 
• 1393731-05-9 C₂₈H₂₀ClN₃O₂S 
• 1393730-93-2 C₂₁H₁₅N₃O₃ 
• 1393731-23-1 C₂₂H₁₈N₂O₄S 
• 1393731-35-5 C₂₈H₂₂N₂O₄S 

Relevant academic research and scientific papers

Synthesis of some new 2-oxo-1,4-disubstituted-1,2,5,6-tetrahydrobenzo[h] quinoline-3-carbonitriles and their biological evaluation as cytotoxic and antiviral agents

A series of new 2-oxo-1,4-disubstituted-1,2,5,6-tetrahydro-benzo[h] quinoline-3-carbonitriles supported with various pharmacophoric functionalities at position-1 is described. N-formyl, N-nitroso, Narylthiocarbamoyl, N-alkyl, N-sulfonyl, and N-acetyl deri

An efficient synthesis of indeno[1,2-b]pyridine and benzo[h]quinoline derivatives under solvent-free conditions

(Chemical Equation Presented) An efficient and convenient multicomponent reaction for the preparation of 4-aryl-2-oxo-2,5-dihydro-1H-indeno[1,2-b] pyridine-3-carbonitrile and 4-aryl-2-oxo-1,2,5,6-tetrahydrobenzo[h]quinoline-3- carbonitrile derivatives by