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Structure of 38940-62-4
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3-Acetyl-5-bromopyridine features a bromine atom at the 5-position and an acetyl group at the 3-position of the pyridine ring, creating a bifunctional scaffold for cross-coupling and derivatization. This electron-deficient heterocycle enables efficient palladium-catalyzed transformations and serves as a building block in medicinal chemistry. The molecule exhibits good stability under standard conditions and facilitates rapid access to functionalized pyridine derivatives.
3-Acetyl-5-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 bromine substituent facilitates C–C bond formation under standard Suzuki-Miyaura or Negishi conditions. Its bench-stable nature and compatibility with diverse reaction conditions make it suitable for iterative synthesis of complex heterocyclic scaffolds and pharmaceutical 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: