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Structure of 1060814-91-6
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Ethyl 2-(4-bromopyridin-2-yl)acetate features a brominated pyridine core paired with an acetyl ester side chain, enabling direct coupling in cross-coupling reactions. This bench-stable building block integrates readily into synthetic sequences requiring halogen-directed functionalization or transition metal catalysis.
Ethyl 2-(4-bromopyridin-2-yl)acetate serves as a versatile building block in cross-coupling chemistry, enabling efficient palladium-catalyzed transformations to access functionalized pyridine derivatives. The bromopyridine moiety facilitates Suzuki, Stille, and Negishi couplings, while the ester group offers orthogonal reactivity for further derivatization. Bench-stable and readily purified by column chromatography, it functions reliably in medicinal chemistry campaigns and process development workflows.
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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: