3-Quinolinecarboxylicacid, 6-bromo-4-hydroxy CAS:122794-99-4
3-Quinolinecarboxylic acid, 6-bromo-4-hydroxy has several important applications primarily in the fields of medicinal chemistry, organic synthesis, and materials science. One of the significant uses of this compound is in drug discovery, where it serves as a lead compound or scaffold for the development of novel pharmaceuticals. The modified quinoline structure can exhibit antimicrobial, anti-inflammatory, and anticancer properties, which are valuable for therapeutic interventions. In organic synthesis, this compound is utilized as a versatile intermediate for the preparation of more complex molecules. The functional groups present in 6-bromo-4-hydroxy allow for various chemical transformations, including substitutions and couplings, which can lead to the synthesis of biologically active compounds. Researchers often explore its reactivity to develop new synthetic pathways that enhance efficiency and selectivity. Additionally, 3-quinolinecarboxylic acid, 6-bromo-4-hydroxy is investigated for its potential applications in materials science. Its unique scaffold may be incorporated into polymer systems or nanomaterials, contributing to advances in sensor technology, light-emitting devices, and catalytic systems. The integration of such compounds can lead to enhanced performance characteristics in these applications. Overall, the diverse utility of 3-quinolinecarboxylic acid, 6-bromo-4-hydroxy demonstrates its significance in various research domains, highlighting its role in advancing both scientific understanding and practical applications.
Composition | C12H10BrNO3 |
Assay | 99% |
Appearance | white powder |
CAS No. | 122794-99-4 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |