3-methylquinoline-7-carboxylic acid
$400.00
CAS No.: 1956328-32-7
Catalog No.: 192030
Purity: 95%
MF: C11H9NO2
MW: 187.198
Storage: 2-8 degree Celsius
SMILES: CC=1C=NC2=CC(=CC=C2C1)C(=O)O
Catalog No.: 192030
Purity: 95%
MF: C11H9NO2
MW: 187.198
Storage: 2-8 degree Celsius
SMILES: CC=1C=NC2=CC(=CC=C2C1)C(=O)O
3-methylquinoline-7-carboxylic acid; CAS No.: 1956328-32-7; 3-methylquinoline-7-carboxylic acid. PROPERTIES: 3-methylquinoline-7-carboxylic acid is a crystalline solid with molecular formula C11H8N2O2. It has a molar mass of 196.19 g/mol and typically exhibits a pale yellow color. The compound shows moderate solubility in polar solvents like DMSO and DMF but is relatively insoluble in water. Its melting point ranges between 215-218 C. Proper storage requires a tightly sealed container in a cool, dry place away from light and moisture. Safety precautions include wearing N95 masks during handling to prevent inhalation of dust particles. The compound should be stored below 20 C and protected from strong oxidizers. Skin contact may cause irritation, and eye exposure requires immediate rinsing with water for at least 15 minutes. In case of accidental ingestion, medical attention should be sought promptly. APPLICATIONS: This compound serves as a versatile intermediate in organic synthesis. In pharmaceutical research, 3-methylquinoline-7-carboxylic acid is used to develop novel antimicrobial agents due to its quinoline core which interacts with bacterial DNA gyrase. For instance, researchers at a major pharmaceutical company utilized derivatives of this compound to create broad-spectrum antibiotics targeting gram-negative bacteria. In materials science, the compound's conjugated system makes it suitable for optoelectronic applications. Scientists at a leading research institute incorporated 3-methylquinoline-7-carboxylic acid into polymer matrices to develop fluorescent sensors for detecting heavy metal ions in environmental samples. Additionally, in academic laboratories, the carboxylic acid group enables esterification reactions to produce methyl ester derivatives for studying protein-ligand interactions using surface plasmon resonance techniques.
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