5-Bromo-3-fluoroquinoline is a heterocyclic organic compound that belongs to the quinoline family, characterized by a fused bicyclic structure containing a benzene ring and a pyridine ring. The presence of bromine and fluorine substituents at the 5 and 3 positions, respectively, significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular structure contributes to its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as quinolines are known for their biological activity, including antimicrobial and antimalarial properties. The presence of halogen atoms can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 5-Bromo-3-fluoroquinoline may undergo various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

5-Bromo-3-fluoroquinoline

1416440-63-5: 5-Bromo-3-fluoroquinoline is a heterocyclic organic compound that belongs to the quinoline family, characterized by a fused bicyclic structure containing a benzene ring and a pyridine ring. The presence of bromine and fluorine substituents at the 5 and 3 positions, respectively, significantly influences its chemical properties and reactivity. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents. Its molecular structure contributes to its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as quinolines are known for their biological activity, including antimicrobial and antimalarial properties. The presence of halogen atoms can enhance the compound's lipophilicity and influence its interaction with biological targets. Additionally, 5-Bromo-3-fluoroquinoline may undergo various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

CAS 1416440-63-5

5-Bromo-3-fluoroquinoline

Quinoline, 5-bromo-3-fluoro-

Ref: IN-DA001GT0

5-Bromo-3-fluoroquinoline

Ref: 54-PC102487

5-BROMO-3-FLUOROQUINOLINE

Ref: 10-F305852

CAS 1416440-63-5

5-Bromo-3-fluoroquinoline

Quinoline, 5-​bromo-​3-​fluoro-

Ref: IN-DA001GT0

5-Bromo-3-fluoroquinoline

Ref: 54-PC102487

5-BROMO-3-FLUOROQUINOLINE

Ref: 10-F305852

Quinoline, 5-bromo-3-fluoro-