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Structure of 174666-22-9
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Ethyl 2-(6-chloropyridin-2-yl)acetate features a chloropyridine moiety linked to an ethyl acetate group, enabling direct incorporation into heterocyclic scaffolds. This bench-stable reagent facilitates efficient coupling reactions in synthetic routes toward bioactive molecules, particularly in medicinal chemistry applications requiring electron-deficient pyridine frameworks.
Ethyl 2-(6-chloropyridin-2-yl)acetate serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-containing scaffolds. Its electrophilic acyl moiety facilitates nucleophilic substitution and coupling reactions, while the 6-chloropyridine handle supports palladium-catalyzed cross-coupling transformations. The compound exhibits excellent bench stability, ease of purification, and functional group tolerance, making it well-suited for iterative synthesis campaigns in API development.
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GHS Pictogram :
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: