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Structure of 164464-60-2
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Ethyl 2-(2-chloropyridin-3-yl)acetate features a chloropyridine moiety linked to an ethyl ester group, enabling direct incorporation into cross-coupling and functionalization reactions. This bench-stable reagent delivers efficient access to substituted pyridine derivatives under standard conditions.
Ethyl 2-(2-chloropyridin-3-yl)acetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized pyridine derivatives. The molecule combines a reactive ester group with an electrophilic 2-chloropyridin-3-yl moiety, facilitating nucleophilic substitution and transition-metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it ideal for use in medicinal chemistry and process development workflows.
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Lot numbers can be found on the outside label of a product: