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Structure of 84199-61-1
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3-Acetyl-2-bromopyridine features a bromine atom at the 2-position and an acetyl group at the 3-position on a pyridine core, enabling selective functionalization in heterocyclic synthesis. This electron-deficient scaffold integrates readily into cross-coupling reactions and serves as a key intermediate for bioactive nitrogen-containing compounds.
3-Acetyl-2-bromopyridine serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions and nucleophilic substitution processes. The acetyl group provides a handle for further functionalization via oxidation or enolization, while the bromide facilitates coupling with arylboranes and other nucleophiles. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: