3,6-Dibromoquinolin-4-ol is a chemical compound characterized by its quinoline structure, which features a bicyclic aromatic system. The presence of two bromine atoms at the 3 and 6 positions of the quinoline ring significantly influences its chemical properties, including its reactivity and solubility. The hydroxyl group (-OH) at the 4-position contributes to its potential as a phenolic compound, enhancing its ability to participate in hydrogen bonding and making it more polar. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in various fields, including organic synthesis and materials science. Additionally, the bromine substituents can facilitate further functionalization, allowing for the development of derivatives with tailored properties. As with many brominated compounds, considerations regarding environmental impact and toxicity are important, particularly in terms of persistence and bioaccumulation. Overall, 3,6-dibromoquinolin-4-ol represents a versatile scaffold for further chemical exploration.

3,6-dibromoquinolin-4-ol

857758-88-4: 3,6-Dibromoquinolin-4-ol is a chemical compound characterized by its quinoline structure, which features a bicyclic aromatic system. The presence of two bromine atoms at the 3 and 6 positions of the quinoline ring significantly influences its chemical properties, including its reactivity and solubility. The hydroxyl group (-OH) at the 4-position contributes to its potential as a phenolic compound, enhancing its ability to participate in hydrogen bonding and making it more polar. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in various fields, including organic synthesis and materials science. Additionally, the bromine substituents can facilitate further functionalization, allowing for the development of derivatives with tailored properties. As with many brominated compounds, considerations regarding environmental impact and toxicity are important, particularly in terms of persistence and bioaccumulation. Overall, 3,6-dibromoquinolin-4-ol represents a versatile scaffold for further chemical exploration.

CAS 857758-88-4

3,6-dibromoquinolin-4-ol

3,6-Dibromo-4-hydroxyquinoline

Ref: 54-OR1075355