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Structure of 944268-58-0
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1-(2-Bromo-3-methylphenyl)ethanone features a brominated aromatic ring fused to an acetyl group, enabling direct functionalization in cross-coupling reactions. The ortho-bromo substituent facilitates palladium-catalyzed transformations, while the methyl group provides steric and electronic modulation. This ketone serves as a key intermediate in pharmaceutical synthesis and materials chemistry, offering predictable reactivity under standard conditions.
1-(2-Bromo-3-methylphenyl)ethanone serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. The bromo group enables palladium-catalyzed cross-coupling reactions, while the acetyl functionality provides a handle for further functionalization via enolization or nucleophilic substitution. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient assembly of complex scaffolds in API 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: