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Structure of 55899-41-7
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Pyrazolo[1,5-a]pyridine-4-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 4-position, enabling direct conjugation in bioactive molecule design. The electron-deficient pyrazolo[1,5-a]pyridine scaffold enhances binding affinity in kinase inhibitors and other targeted therapeutics. This bench-stable, moisture-tolerant compound integrates readily into synthetic sequences for pharmaceutical intermediates and functional materials.
Pyrazolo[1,5-a]pyridine-4-carboxylic acid serves as a versatile scaffold for medicinal chemistry and materials science, offering a rigid, heteroaromatic core with defined hydrogen-bonding capacity via its carboxylic acid group. The molecule exhibits bench stability, facilitates straightforward derivatization through amide and ester formation, and functions effectively in coupling reactions. Its structural motif is well-documented in bioactive compound libraries, enabling rapid access to functionalized analogs for target validation and lead optimization.
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Lot numbers can be found on the outside label of a product: