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Structure of 2524-52-9
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Ethyl 2-picolinate is a bench-stable, moisture-tolerant ester featuring a pyridine ring with a strategically positioned ester group. This configuration enables direct incorporation into heterocyclic synthesis and facilitates transition metal-catalyzed coupling reactions. The electron-deficient pyridine ring enhances reactivity in nucleophilic substitution processes, while the ethyl ester moiety offers improved solubility in common organic solvents.
Ethyl 2-picolinate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to pyridine-based heterocycles and pharmaceutical intermediates. Its ester functionality facilitates nucleophilic acyl substitution and subsequent transformations, while the picolinate core provides a rigid, electron-deficient scaffold compatible with cross-coupling reactions. Bench-stable and readily purified by distillation or chromatography, it functions reliably in multistep syntheses requiring functional group tolerance and predictable reactivity.
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Lot numbers can be found on the outside label of a product: