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Structure of 86447-11-2
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1-Boc-1,2,5,6-tetrahydropyridine-3-carboxylic acid serves as a stable, bench-ready precursor for functionalized tetrahydropyridine scaffolds. The Boc group enables selective deprotection under mild acidic conditions, while the carboxylic acid moiety facilitates conjugation via amide or ester linkages. This compound integrates readily into synthetic sequences requiring nitrogen-containing heterocycles with controlled reactivity and enhanced solubility in organic media.
1-Boc-1,2,5,6-tetrahydropyridine-3-carboxylic acid serves as a versatile building block for the synthesis of substituted tetrahydropyridine scaffolds prevalent in medicinal chemistry. The Boc group provides excellent stability and orthogonal deprotection compatibility, enabling controlled functionalization at the nitrogen. The carboxylic acid moiety facilitates coupling reactions with amines and alcohols under standard conditions, supporting efficient access to diverse analogs. Its bench-stable nature and predictable reactivity make it ideal for multi-step syntheses and process development.
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Lot numbers can be found on the outside label of a product: