33274-47-4

Usage

Uses

Used in Pharmaceutical Industry:
6-METHYL-2-OXO-1,2-DIHYDRO-4-QUINOLINECARBOXYLIC ACID is used as a building block for the synthesis of various drugs and pharmaceuticals due to its unique chemical structure and functional groups.
Used in Anti-Inflammatory Medications:
In the pharmaceutical industry, 6-METHYL-2-OXO-1,2-DIHYDRO-4-QUINOLINECARBOXYLIC ACID is used as an intermediate for the development of anti-inflammatory medications, contributing to the treatment of various inflammatory conditions.
Used in Antimalarial Medications:
6-METHYL-2-OXO-1,2-DIHYDRO-4-QUINOLINECARBOXYLIC ACID is utilized as a key component in the synthesis of antimalarial drugs, playing a crucial role in combating malaria infections.
Used in Antibacterial Medications:
6-METHYL-2-OXO-1,2-DIHYDRO-4-QUINOLINECARBOXYLIC ACID is also used as an intermediate in the production of antibacterial medications, aiding in the fight against bacterial infections.
Used in Research and Development:
6-METHYL-2-OXO-1,2-DIHYDRO-4-QUINOLINECARBOXYLIC ACID has potential applications in research and development for the discovery and creation of new medicines and compounds, owing to its distinctive chemical properties and structure.

InChI:InChI=1/C11H9NO3/c1-6-2-3-9-7(4-6)8(11(14)15)5-10(13)12-9/h2-5H,1H3,(H,12,13)(H,14,15)

Upstream product

• 118726-65-1 5-methyl-1-acetyl-2,3-dihydro-1H-indole-2,3-dione 
• 608-05-9 5-methyl-indole-2,3-dione 
• 141-82-2 malonic acid 

Downstream Products

• 697236-17-2 2-(2-chlorobenzyloxy)-4-(2-chlorobenzyloxycarbonyl)-6-methylquinoline 
• 855165-89-8 6-methyl-2-oxo-1,2,3,4-tetrahydroquinoline-4-carboxylic acid 
• 50503-75-8 2-chloro-6-methyl-quinoline-4-carboxylic acid 

Relevant academic research and scientific papers

Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents

A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent.

Synthesis of substituted 1,2,3,4-tetrahydroquinoline-4-carboxylic acids

Reduction of some substituted quinoline-4-carboxylic acids was studied. The reduction of 2-alkylquinoline-4-carboxylic acids with Raney nickel in aqueous alkali was stereoselective, and the resulting 2-alkyl-1,2,3,4- tetrahydroquinoline-4-carboxylic acids

Use of imidazo?1,5-a!quinolones as neuroprotective agents

The imidazo?1,5-a!quinolines (I) are useful in treating neurological diseases/conditions or chronic neurodegenerative diseases/conditions.

Imidazo[1,5-A]quinolines for treatment of anxiety and sleep disorders

Imidazo[1,5-a]quinolines of formula (I) which are useful pharmaceutical agents for the treatment of anxiety, sleep disorders, panic states, convulsions and muscle disorders. STR1

Certain 2-oxo-quinoline carboxylates or corresponding carboxamides useful as anti-emetics and suppressants of migraine

There is disclosed a heterocyclic compound represented by general formula: STR1 wherein R1 represents hydrogen, lower alkyl or aryl; R2 represents hydrogen, hydroxyl or lower alkyl; A represents CH or N; X represents --O-- or --NH--; R3 represents hydrogen, hydroxyl or lower alkyl; R4 represents lower alkyl; represents 0 or 1, or a pharmaceutically acceptable salt thereof.

5-HT3 Receptor Antagonists. 1. New Quinoline Derivatives

A series of esters and amides of 1-alkyl-2-oxo-1,2-dihydroquinoline-4-carboxylic acid or 2-alkoxyquinoline-4-carboxylic acid containing a basic azabicycloalkyl moiety has been synthesized and evaluated for affinity for the 3H>quipazine-labeled