6-Bromo-2-chloro-3-ethylquinoline is a heterocyclic organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of bromine and chlorine substituents at the 6 and 2 positions, respectively, along with an ethyl group at the 3 position, contributes to its unique chemical properties. This compound is typically a pale yellow to brown solid and is soluble in organic solvents. It may exhibit biological activity, making it of interest in medicinal chemistry and drug development. The halogen substituents can influence its reactivity, potentially allowing for further functionalization or participation in various chemical reactions, such as nucleophilic substitutions or coupling reactions. Additionally, the compound's structure may impart specific electronic properties, affecting its interaction with biological targets. Safety and handling precautions should be observed due to the presence of halogens, which can pose health risks. Overall, 6-bromo-2-chloro-3-ethylquinoline represents a versatile scaffold for further chemical exploration and application in various fields.

6-bromo-2-chloro-3-ethylquinoline

409346-70-9: 6-Bromo-2-chloro-3-ethylquinoline is a heterocyclic organic compound characterized by its quinoline structure, which consists of a fused benzene and pyridine ring. The presence of bromine and chlorine substituents at the 6 and 2 positions, respectively, along with an ethyl group at the 3 position, contributes to its unique chemical properties. This compound is typically a pale yellow to brown solid and is soluble in organic solvents. It may exhibit biological activity, making it of interest in medicinal chemistry and drug development. The halogen substituents can influence its reactivity, potentially allowing for further functionalization or participation in various chemical reactions, such as nucleophilic substitutions or coupling reactions. Additionally, the compound's structure may impart specific electronic properties, affecting its interaction with biological targets. Safety and handling precautions should be observed due to the presence of halogens, which can pose health risks. Overall, 6-bromo-2-chloro-3-ethylquinoline represents a versatile scaffold for further chemical exploration and application in various fields.

CAS 409346-70-9

6-bromo-2-chloro-3-ethylquinoline

6-Bromo-2-chloro-3-ethylquinoline

Ref: IN-DA00CL9V

6-Bromo-2-chloro-3-ethylquinoline

Ref: 54-OR309270

6-Bromo-2-chloro-3-ethylquinoline

Ref: 10-F602277