CAS 19499-19-5: ETHYL 4,7-DICHLOROQUINOLINE-3-CARBOXYLATE

Description: Ethyl 4,7-dichloroquinoline-3-carboxylate is a chemical compound characterized by its quinoline structure, which features a bicyclic aromatic system. This compound contains two chlorine substituents at the 4 and 7 positions of the quinoline ring, contributing to its unique reactivity and potential biological activity. The ethyl ester functional group at the carboxylic acid position enhances its solubility in organic solvents, making it useful in various chemical reactions and applications. Ethyl 4,7-dichloroquinoline-3-carboxylate may exhibit antimicrobial or antimalarial properties, as many quinoline derivatives are known for their pharmacological activities. Its molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the presence of chlorine atoms can influence the compound's lipophilicity and metabolic stability. Safety and handling precautions should be observed due to the potential toxicity associated with chlorine-containing compounds. Overall, this compound represents a significant class of heterocyclic compounds with diverse applications in research and industry.

Formula: C₁₂H₉Cl₂NO₂

ETHYL 4,7-DICHLOROQUINOLINE-3-CARBOXYLATE

CAS: 19499-19-5

• Formula: C₁₂H₉Cl₂NO₂
• Molecular weight: 270.1114

Ethyl 4,7-dichloroquinoline-3-carboxylate

CAS: 19499-19-5

• Purity: 95+%
• Molecular weight: 270.1099853515625

Ethyl4,7-dichloroquinoline-3-carboxylate

CAS: 19499-19-5

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• Formula: C₁₂H₉Cl₂NO₂
• Purity: Min. 95%
• Molecular weight: 270.11 g/mol