CAS 635-79-0

2-Methyl-3-quinolinecarboxylic acid

Description:

2-Methyl-3-quinolinecarboxylic acid, with the CAS number 635-79-0, is an organic compound belonging to the class of quinoline derivatives. It features a quinoline ring structure, which is a bicyclic compound composed of a benzene ring fused to a pyridine ring. This compound is characterized by the presence of a carboxylic acid functional group (-COOH) and a methyl group (-CH3) at the 2 and 3 positions of the quinoline ring, respectively. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. The compound is of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activities and applications in synthesizing other chemical entities. Additionally, it may exhibit properties such as fluorescence or specific reactivity patterns, making it useful in research and development. Safety data should be consulted for handling and storage, as with any chemical substance.

Formula: C₁₁H₉NO₂

InChI: InChI=1S/C11H9NO2/c1-7-9(11(13)14)6-8-4-2-3-5-10(8)12-7/h2-6H,1H3,(H,13,14)

InChI key: InChIKey=WXYKQNAKEPRCGF-UHFFFAOYSA-N

SMILES: C(O)(=O)C1=CC2=C(N=C1C)C=CC=C2

Synonyms:

• 2-Methyl-3-quinolinecarboxylic acid
• 3-Quinolinecarboxylic Acid, 2-Methyl-
• 2-Methylquinoline-3-carboxylic acid

2-Methyl-quinoline-3-carboxylic acid

CAS: 635-79-0

Formula: C₁₁H₉NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 187.1947

Ref: IN-DA00EIV6

2-Methylquinoline-3-carboxylic acid

CAS: 635-79-0

2-Methylquinoline-3-carboxylic acid

Formula: C₁₁H₉NO₂

Purity: 95%

Color and Shape: light brown to brown solid

Molecular weight: 187.19g/mol

Ref: 54-OR301188

2-Methylquinoline-3-carboxylic acid

CAS: 635-79-0

Formula: C₁₁H₉NO₂

Purity: 97%

Color and Shape: Liquid, No data available.

Molecular weight: 187.198

Ref: 10-F223784

2-Methylquinoline-3-carboxylic acid

CAS: 635-79-0

2-Methylquinoline-3-carboxylic acid (2MQCA) is a nucleophilic, acidic and hiv integrase inhibitor. It has been shown to inhibit the activity of HIV integrase by binding to the active site of the enzyme. 2MQCA has a strong affinity for chloride ions and is soluble in organic solvents such as diethyl ether or chloroform. 2MQCA shows diffraction peaks at 2.5Å, which is indicative of an acidic molecule with a hydroxymethyl group. Reaction time for a reaction between 2MQCA and methylamine was found to be optimal at 10 minutes at room temperature and pH 5. The technique used for this reaction was NMR spectroscopy.

Formula: C₁₁H₉NO₂

Purity: Min. 95%

Molecular weight: 187.2 g/mol

Ref: 3D-AAA63579