Chemical compounds are the fundamental building blocks of scientific inquiry, and understanding their properties is crucial for unlocking their full potential. CAS 1172534-83-6, scientifically known as 6-Bromo-7-methyl[1,2,4]triazolo[1,5-a]pyridine, is one such compound that has garnered attention in various research domains. This article aims to elucidate its key chemical properties and explore its diverse research applications, highlighting its significance in fields ranging from organic synthesis to medicinal chemistry.

At its core, 6-Bromo-7-methyl[1,2,4]triazolo[1,5-a]pyridine is a heterocyclic compound belonging to the triazolopyridine family. Its molecular formula is C7H6BrN3, and it possesses a molecular weight of approximately 212.05 g/mol. The presence of the bromine atom at the 6-position and a methyl group at the 7-position are key structural features that dictate its reactivity and potential applications. The bromine atom, being an electron-withdrawing group, can influence the electron density distribution across the aromatic system, making specific positions more susceptible to nucleophilic or electrophilic attack. It also serves as a crucial handle for various synthetic transformations, most notably cross-coupling reactions.

The triazolopyridine scaffold itself is a nitrogen-rich bicyclic system known for its stability and ability to interact with biological targets. This makes derivatives like 6-Bromo-7-methyl[1,2,4]triazolo[1,5-a]pyridine valuable in the search for new pharmaceutical agents. While specific direct applications are still being explored, related compounds within the triazolopyridine class have demonstrated significant biological activities, including inhibitory effects on enzymes and receptors crucial for various physiological processes. Researchers often utilize this compound as a starting point for medicinal chemistry programs, aiming to synthesize novel analogs with enhanced therapeutic properties.

In terms of synthetic applications, CAS 1172534-83-6 serves as a versatile intermediate. Its structure allows for modifications at multiple sites, enabling the construction of complex molecular architectures. For instance, the bromine atom can be readily replaced through nucleophilic substitution reactions or utilized in metal-catalyzed cross-coupling reactions to introduce diverse organic fragments. This versatility makes it a prized compound for chemists looking to synthesize libraries of compounds for screening or to build specific, complex target molecules.

The purity of chemical intermediates is paramount for reproducible research results. Suppliers like NINGBO INNO PHARMCHEM CO.,LTD. ensure that compounds such as 6-Bromo-7-methyl[1,2,4]triazolo[1,5-a]pyridine are provided at high purity levels, often exceeding 97%. This commitment to quality is essential for researchers worldwide who rely on consistent and reliable chemical reagents. When sourcing this compound, researchers might use terms like '6-Bromo-7-methyl[1,2,4]triazolo[1,5-a]pyridine supplier' or 'CAS 1172534-83-6 chemical information' to find reliable sources.

In conclusion, 6-Bromo-7-methyl[1,2,4]triazolo[1,5-a]pyridine (CAS 1172534-83-6) is a compound of considerable interest in the chemical sciences. Its unique structural features, combined with its reactivity and potential biological relevance, position it as a valuable tool for advancing organic synthesis and exploring new avenues in drug discovery and development.