Methyl 4-chloro-8-fluoroquinoline-2-carboxylate is a synthetic organic compound belonging to the quinoline family, characterized by its heterocyclic structure that includes both chlorine and fluorine substituents. This compound typically exhibits a pale yellow to off-white crystalline appearance. It is known for its potential biological activity, particularly in medicinal chemistry, where quinoline derivatives are often explored for their antimicrobial, antimalarial, and anticancer properties. The presence of the methyl ester functional group enhances its solubility in organic solvents, which can be advantageous for various applications in drug formulation. Additionally, the chlorine and fluorine atoms contribute to the compound's lipophilicity and may influence its pharmacokinetic properties. Methyl 4-chloro-8-fluoroquinoline-2-carboxylate is generally handled with care due to its potential reactivity and the need for proper safety protocols in laboratory settings. As with many chemical substances, its stability, reactivity, and biological effects can vary based on environmental conditions and specific formulations.

methyl4-chloro-8-fluoroquinoline-2-carboxylate

219949-90-3: Methyl 4-chloro-8-fluoroquinoline-2-carboxylate is a synthetic organic compound belonging to the quinoline family, characterized by its heterocyclic structure that includes both chlorine and fluorine substituents. This compound typically exhibits a pale yellow to off-white crystalline appearance. It is known for its potential biological activity, particularly in medicinal chemistry, where quinoline derivatives are often explored for their antimicrobial, antimalarial, and anticancer properties. The presence of the methyl ester functional group enhances its solubility in organic solvents, which can be advantageous for various applications in drug formulation. Additionally, the chlorine and fluorine atoms contribute to the compound's lipophilicity and may influence its pharmacokinetic properties. Methyl 4-chloro-8-fluoroquinoline-2-carboxylate is generally handled with care due to its potential reactivity and the need for proper safety protocols in laboratory settings. As with many chemical substances, its stability, reactivity, and biological effects can vary based on environmental conditions and specific formulations.

CAS 219949-90-3

methyl4-chloro-8-fluoroquinoline-2-carboxylate

Methyl 4-chloro-8-fluoroquinoline-2-carboxylate

Ref: 3D-UIA94990