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Structure of 37074-40-1
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1-(4-Bromo-3-methylphenyl)ethanone features a brominated aromatic ring flanked by a methyl group and a ketone-bearing side chain, enabling direct integration into cross-coupling and functionalization workflows. The electron-deficient aryl moiety pairs effectively with palladium catalysts under standard conditions, while the bench-stable ketone offers a reliable handle for further derivatization in synthetic sequences.
1-(4-Bromo-3-methylphenyl)ethanone serves as a versatile building block for the synthesis of biologically active molecules and pharmaceutical intermediates. Its structure features a brominated aromatic ring with a methyl group in close proximity to a ketone functionality, enabling selective functionalization via cross-coupling reactions. The ketone group provides a handle for further transformations such as reduction, nucleophilic addition, or enolization, while the aryl bromide supports palladium-catalyzed coupling processes. Bench-stable and readily purified by recrystallization or column chromatography, it integrates efficiently into multi-step synthetic sequences.
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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: