102028-51-3

Basic information

• Product Name: 3-Quinolinecarboxylic acid, 1,2-dihydro-2-oxo-4-phenyl-, ethyl ester
• CAS NO: 102028-51-3
• Molecular Formula: C18H15NO3
• Molecular Weight: 293.322
• Mol File: 102028-51-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 3-Quinolinecarboxylic acid, 1,2-dihydro-2-oxo-4-phenyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Quinolinecarboxylic acid, 1,2-dihydro-2-oxo-4-phenyl-, ethyl ester(102028-51-3)
• EPA Substance Registry System: 3-Quinolinecarboxylic acid, 1,2-dihydro-2-oxo-4-phenyl-, ethyl ester(102028-51-3)

Safety Data

• Hazardous Substances Data: 102028-51-3(Hazardous Substances Data)

Upstream product

• 1071-46-1 hydrogen ethyl malonate 
• 2835-77-0 (2-aminophenyl)(phenyl)methanone 
• 105-53-3 diethyl malonate 
• 4688-74-8 phenylboric acid 
• 99429-64-8 ethyl ester of 4-chloro-2-oxo-1,2-dihydroquinoline-3-carboxylic acid 
• 6315-94-2 ethyl 2,4-dichloroquinoline-3-carboxylate 
• 36239-09-5 ethyl chlorocarbonylacetate 
• 134-20-3 2-carbomethoxyaniline 
• 53341-66-5 ethyl 3-oxo-3-(phenylamino)propionate 
• 131781-56-1 ethyl 2-oxo-4-phenyl-1,2,3,4-tetrahydroquinoline-3-carboxylate 
• 62-53-3 aniline 
• 178215-63-9 N-(2-Benzoyl-phenyl)-malonamic acid ethyl ester 

Downstream Products

• 1601219-71-9 N-(1-benzylpiperidin-4-yl)-2-oxo-4-phenyl-1,2-dihydroquinoline-3-carboxamide 
• 81698-18-2 ethyl 1-methyl-2-oxo-4-phenyl-1,2-dihydroquinoline-3-carboxylate 
• 92795-47-6 2-oxo-4-phenyl-1,2-dihydroquinoline-3-carboxylic acid 
• 138712-66-0 2-chloro-3-chloromethyl-4-phenylquinoline 
• 140842-11-1 3-benzoyloxymethyl-2-(4-methyl-1-piperazinyl)-4-phenylquinoline 
• 140842-10-0 3-n-butoxymethyl-2-(4-methyl-1-piperazinyl)-4-phenylquinoline 
• 140842-09-7 3-hydroxymethyl-2-(4-methyl-1-piperazinyl)-4-phenylquinoline 

Relevant articles and documents

Synthesis and biological evaluation of dihydroquinoline carboxamide derivatives as anti-tubercular agents

Sodium trifluoromethanesulfonate, and glacial acetic acid selectively catalyzed the synthesis of dihydroquinoline via Friedl?nder annulation. The synthesized dihydroquinoline analogues coupled with different amines by the use of coupling reagent gave dihy

AlCl 3 -Mediated Synthesis of 4-Aryl-2-quinolone-3-carboxylates

4-Aryl-2-quinolones are important skeletons from both chemical and medicinal viewpoints. We herein report the development of an efficient synthetic method for 3-substituted 4-aryl-2-quinolones. The key reaction in this process involves an AlCl 3/sub

One-pot microwave-assisted synthesis of 3,4-disubstituted 2-quinolinones

An improved one-pot synthesis of 3,4-disubstituted 2-quinolinones is described. The condensation of substituted 2-aminobenzophenone (or 2-aminophenyl alkyl ketone) with acid chlorides was carried out in the presence of triethylamine (or NaH) under microwa