CAS 59394-30-8
:2-Quinolinecarboxylic acid, 6-chloro-
Description:
2-Quinolinecarboxylic acid, 6-chloro- is an aromatic compound characterized by a quinoline structure, which consists of a fused benzene and pyridine ring. The presence of a carboxylic acid functional group (-COOH) at the 2-position and a chlorine atom at the 6-position contributes to its unique chemical properties. This compound typically exhibits moderate solubility in polar solvents due to the carboxylic acid group, while its aromatic nature allows for potential interactions with other aromatic systems. It may participate in various chemical reactions, including electrophilic substitution and carboxylation. The chlorine substituent can influence the reactivity and stability of the compound, making it of interest in synthetic organic chemistry and medicinal chemistry. Additionally, derivatives of quinolinecarboxylic acids are often studied for their biological activities, including antimicrobial and anti-inflammatory properties. As with many chemical substances, safety precautions should be observed when handling this compound, as it may pose health risks if ingested or inhaled.
Formula:C10H6ClNO2
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Found 4 products.
6-Chloroquinoline-2-carboxylic acid
CAS:Formula:C10H6ClNO2Purity:97%Color and Shape:SolidMolecular weight:207.61316-Chloroquinoline-2-carboxylic acid
CAS:6-Chloroquinoline-2-carboxylic acidPurity:97%Molecular weight:207.61g/mol6-CHLOROQUINOLINE-2-CARBOXYLIC ACID
CAS:Formula:C10H6ClNO2Purity:97%Color and Shape:Liquid, No data available.Molecular weight:207.616-chloroquinoline-2-carboxylic acid
CAS:<p>6-chloroquinoline-2-carboxylic acid is a metabolite that is formed by the coupling of two molecules of ethanolamide. The coupling reaction was first developed by Miyaura and Suzuki in 1980. 6-Chloroquinaline-2-carboxylic acid is used in marine chemistry to synthesize tetracyclic molecules with a side chain.</p>Formula:C10H6ClNO2Purity:Min. 95%Molecular weight:207.61 g/mol



