2-Chloro-3-(2-chloroethyl)-6-ethoxy-quinoline is a synthetic organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. This compound features two chlorine substituents and an ethoxy group, contributing to its chemical reactivity and potential biological activity. The presence of the chloroethyl group suggests that it may participate in nucleophilic substitution reactions, making it of interest in medicinal chemistry for potential therapeutic applications. The ethoxy group enhances its lipophilicity, which can influence its solubility and permeability in biological systems. Additionally, the quinoline structure is known for its diverse pharmacological properties, including antimicrobial and antimalarial activities. The compound's specific interactions and effects would depend on its molecular conformation and the presence of functional groups, making it a candidate for further investigation in drug development and chemical research. As with many synthetic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

2-chloro-3-(2-chloroethyl)-6-ethoxy-quinoline

948294-49-3: 2-Chloro-3-(2-chloroethyl)-6-ethoxy-quinoline is a synthetic organic compound characterized by its quinoline backbone, which is a bicyclic structure containing a benzene ring fused to a pyridine ring. This compound features two chlorine substituents and an ethoxy group, contributing to its chemical reactivity and potential biological activity. The presence of the chloroethyl group suggests that it may participate in nucleophilic substitution reactions, making it of interest in medicinal chemistry for potential therapeutic applications. The ethoxy group enhances its lipophilicity, which can influence its solubility and permeability in biological systems. Additionally, the quinoline structure is known for its diverse pharmacological properties, including antimicrobial and antimalarial activities. The compound's specific interactions and effects would depend on its molecular conformation and the presence of functional groups, making it a candidate for further investigation in drug development and chemical research. As with many synthetic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

2-Chloro-3-(2-chloroethyl)-6-ethoxyquinoline

CAS 948294-49-3

2-chloro-3-(2-chloroethyl)-6-ethoxy-quinoline

2-Chloro-3-(2-chloroethyl)-6-ethoxyquinoline

Ref: 54-OR307895