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Structure of 857653-92-0
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This pyridyl-substituted oxadiazole derivative features a reactive methanamine handle for conjugation, enabling direct integration into bioconjugation workflows. The electron-deficient oxadiazole ring enhances stability under standard conditions, while the para-pyridyl group provides directional polarity for modular synthesis applications.
1-[3-(Pyridin-4-yl)-1,2,4-oxadiazol-5-yl]methanamine serves as a versatile building block for constructing bioactive heterocyclic scaffolds. Its pyridyl-oxadiazole motif enables robust conjugation in medicinal chemistry campaigns, offering enhanced solubility and metabolic stability. The primary amine facilitates straightforward derivatization via amidation, alkylation, or coupling reactions. Bench-stable and readily purified by standard chromatography, it functions effectively in multi-step syntheses targeting kinase inhibitors and other targeted therapeutics.
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Lot numbers can be found on the outside label of a product: