6-Bromo-7-chloroquinoline is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of bromine and chlorine substituents at the 6 and 7 positions, respectively, contributes to its unique chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish color and is sparingly soluble in water but more soluble in organic solvents such as ethanol and dimethyl sulfoxide. It may display biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The halogen substituents can influence the compound's electronic properties, potentially enhancing its interactions with biological targets. Additionally, 6-bromo-7-chloroquinoline may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the presence of the halogens. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks. Overall, this compound serves as a valuable building block in synthetic organic chemistry and drug discovery.

6-bromo-7-chloroquinoline

127827-54-7: 6-Bromo-7-chloroquinoline is a heterocyclic organic compound characterized by a quinoline backbone, which consists of a fused benzene and pyridine ring. The presence of bromine and chlorine substituents at the 6 and 7 positions, respectively, contributes to its unique chemical properties and reactivity. This compound typically exhibits a pale yellow to brownish color and is sparingly soluble in water but more soluble in organic solvents such as ethanol and dimethyl sulfoxide. It may display biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The halogen substituents can influence the compound's electronic properties, potentially enhancing its interactions with biological targets. Additionally, 6-bromo-7-chloroquinoline may undergo various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the presence of the halogens. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks. Overall, this compound serves as a valuable building block in synthetic organic chemistry and drug discovery.

CAS 127827-54-7

6-bromo-7-chloroquinoline

Quinoline, 6-bromo-7-chloro-

Ref: IN-DA000XGK