6-Bromo-7-fluoro-3-nitroquinolin-4-ol is a synthetic organic compound belonging to the quinoline family, characterized by its complex aromatic structure. This compound features a bromine atom at the 6-position, a fluorine atom at the 7-position, and a nitro group at the 3-position of the quinoline ring, along with a hydroxyl group at the 4-position. These substituents contribute to its unique chemical properties, including potential biological activity and reactivity. The presence of the nitro group often enhances the compound's electrophilicity, while the halogen atoms can influence its solubility and interaction with biological targets. This compound may exhibit antimicrobial or anticancer properties, making it of interest in medicinal chemistry. Its molecular structure allows for various synthetic modifications, which can be explored for developing derivatives with enhanced efficacy or selectivity. As with many quinoline derivatives, it is essential to handle this compound with care, considering its potential toxicity and the need for appropriate safety measures during synthesis and experimentation.

6-bromo-7-fluoro-3-nitroquinolin-4-ol

1656989-76-2: 6-Bromo-7-fluoro-3-nitroquinolin-4-ol is a synthetic organic compound belonging to the quinoline family, characterized by its complex aromatic structure. This compound features a bromine atom at the 6-position, a fluorine atom at the 7-position, and a nitro group at the 3-position of the quinoline ring, along with a hydroxyl group at the 4-position. These substituents contribute to its unique chemical properties, including potential biological activity and reactivity. The presence of the nitro group often enhances the compound's electrophilicity, while the halogen atoms can influence its solubility and interaction with biological targets. This compound may exhibit antimicrobial or anticancer properties, making it of interest in medicinal chemistry. Its molecular structure allows for various synthetic modifications, which can be explored for developing derivatives with enhanced efficacy or selectivity. As with many quinoline derivatives, it is essential to handle this compound with care, considering its potential toxicity and the need for appropriate safety measures during synthesis and experimentation.

CAS 1656989-76-2

6-bromo-7-fluoro-3-nitroquinolin-4-ol

4-Quinolinol, 6-bromo-7-fluoro-3-nitro-

Ref: IN-DA001WAY

6-Bromo-7-fluoro-3-nitroquinolin-4-ol

Ref: 54-PC1006715

6-Bromo-7-fluoro-3-nitroquinolin-4-ol

Ref: 10-F547689