Methyl 2-aminopyridine-4-carboxylate CAS:6937-03-7

Methyl 2-aminopyridine-4-carboxylate, with the molecular formula C8H10N2O2, is a notable pyridine derivative characterized by the presence of an amino group at the 2-position and a carboxylate ester at the 4-position, along with a methyl group attached to the carboxylic acid. This unique structure imparts a range of interesting chemical properties, making it a valuable compound for various applications in organic and medicinal chemistry. The amino group introduces basicity and nucleophilic character to the molecule, while the carboxylate ester provides sites for further chemical modifications. This positioning allows for diverse reactivity patterns, enabling chemists to use methyl 2-aminopyridine-4-carboxylate as a versatile building block in synthetic pathways. The compound can be employed in diverse reactions, such as amide formation, acylation, and couplings, facilitating the synthesis of more complex molecules. In medicinal chemistry, methyl 2-aminopyridine-4-carboxylate has attracted attention due to its potential bioactivity. Preliminary studies have suggested that the compound may exhibit antimicrobial, anti-inflammatory, and antitumor properties, making it a candidate for further exploration in drug development. The structural features allow it to interact with various biological targets, which could lead to the design of novel therapeutics. Additionally, the compound's role extends beyond pharmaceuticals into agrochemicals and materials science, where it may serve as an intermediate for synthesizing pesticides or functionalized polymers. Overall, methyl 2-aminopyridine-4-carboxylate exemplifies the importance of pyridine derivatives in contemporary chemical research. Its diverse applications and promising biological activities underscore its significance as a compound worth investigating in both academic and industrial settings.