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Structure of 111043-09-5
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1-(3-Bromopyridin-2-yl)ethanone features a brominated pyridine ring coupled to an acetyl group, delivering a reactive electrophilic site for cross-coupling and functionalization. This bench-stable ketone integrates readily into synthetic pathways requiring nitrogen-containing heterocyclic motifs with enhanced reactivity at the 3-position.
1-(3-Bromopyridin-2-yl)ethanone serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-established bromine reactivity. The pyridinone functionality provides orthogonal handle for further derivatization, while the ketone group offers stability and compatibility with standard purification methods. Its bench-stable nature and predictable reactivity make it ideal for constructing complex heterocyclic scaffolds and API intermediates.
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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: