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Structure of 122180-16-9
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This pyridine-based carboxylic acid integrates a methyl-substituted 1,2-dihydropyridinone scaffold with a reactive acetic acid handle. The electron-deficient dihydropyridinone ring enables efficient coupling reactions, while the pendant carboxylate offers convenient derivatization. Bench-stable and moisture-tolerant, this reagent streamlines access to functionalized heterocycles in synthetic and medicinal chemistry workflows.
2-(4-Methyl-2-oxo-1,2-dihydropyridin-1-yl)acetic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyridone-derived scaffolds. Its carboxylic acid functionality facilitates derivatization and conjugation, while the dihydropyridinone core exhibits stability under standard bench conditions. The molecule functions effectively in coupling reactions and provides a platform for constructing biologically relevant frameworks through established synthetic protocols.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: