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Structure of 51054-99-0
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Ethyl 3-bromo-4-pyridineacetate features a brominated pyridine core paired with an ester-functionalized side chain, enabling direct coupling in cross-coupling reactions. This bench-stable reagent integrates readily into synthetic sequences requiring halogen-directed functionalization or transition-metal-catalyzed transformations.
Ethyl 3-bromo-4-pyridineacetate serves as a versatile building block for the synthesis of pyridine-containing pharmaceutical intermediates and functionalized heterocycles. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality offers opportunities for selective reduction or hydrolysis. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for iterative synthetic strategies in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H302-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: