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Structure of 97004-05-2
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(3-Methylpyridin-4-yl)methanamine features a pyridine ring bearing a methyl group at the 3-position and a primary amine attached via a methylene linker at the 4-position. This configuration imparts enhanced solubility and nucleophilicity, enabling efficient incorporation into pharmaceutical scaffolds. The electron-rich aromatic system facilitates transition metal catalysis and supports robust conjugation in bioactive molecule design.
(3-Methylpyridin-4-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive heterocycles through standard coupling and functionalization reactions. Its pyridyl nitrogen and methyl group offer orthogonal reactivity for selective derivatization, while the primary amine facilitates straightforward conjugation and salt formation. The compound exhibits good bench stability and is compatible with common purification methods, making it well-suited for iterative synthesis workflows in drug discovery.
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Lot numbers can be found on the outside label of a product: