CAS 16498-85-4

3-Quinolinecarboxylic acid, 2-chloro-, methyl ester

Description:

3-Quinolinecarboxylic acid, 2-chloro-, methyl ester is an organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. This compound features a carboxylic acid functional group that is esterified with methanol, resulting in a methyl ester. The presence of a chlorine atom at the 2-position of the quinoline ring introduces unique reactivity and influences its physical and chemical properties. Typically, such compounds exhibit moderate solubility in organic solvents and may have limited solubility in water due to their hydrophobic aromatic structure. They can participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, owing to the electron-withdrawing nature of the chlorine substituent. Additionally, derivatives of quinoline compounds are often studied for their biological activities, including potential antimicrobial and anticancer properties. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 3-Quinolinecarboxylic acid, 2-chloro-, methyl ester is a compound of interest in both synthetic organic chemistry and medicinal chemistry.

Formula: C₁₁H₈ClNO₂

3-Quinolinecarboxylic acid, 2-chloro-, methyl ester

CAS: 16498-85-4

Formula: C₁₁H₈ClNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 221.6397

Ref: IN-DA001V7D

Methyl 2-chloroquinoline-3-carboxylate

CAS: 16498-85-4

Methyl 2-chloroquinoline-3-carboxylate

Purity: 95%

Molecular weight: 221.64g/mol

Ref: 54-OR93742

Methyl 2-chloroquinoline-3-carboxylate

CAS: 16498-85-4

Formula: C₁₁H₈ClNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 221.64

Ref: 10-F439730

Methyl 2-chloro-3-quinolinecarboxylate

CAS: 16498-85-4

Methyl 2-chloro-3-quinolinecarboxylate is a heterocycle that inhibits bacterial growth by binding to the DNA gyrase and topoisomerase IV. This antibiotic has been shown to be active against Pseudomonas aeruginosa and other bacteria, including those that are resistant to quinolones. Methyl 2-chloro-3-quinolinecarboxylate binds to the enzyme's active site, inhibiting its function and halting DNA synthesis. It also contains a halogen group that may interact with the enzyme's active site, thereby preventing the formation of an enzyme-substrate complex.

Formula: C₁₁H₈ClNO₂

Purity: Min. 95%

Molecular weight: 221.64 g/mol

Ref: 3D-RAA49885