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Structure of 103286-27-7
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1-(2-Bromo-4-methylphenyl)ethanone features a brominated aromatic ring fused to an acetyl group, enabling direct functionalization in cross-coupling reactions. The para-methyl substitution enhances electron density at the ipso position, while the bromine serves as a reactive handle for palladium-catalyzed transformations. This compound demonstrates excellent stability under standard bench conditions and integrates readily into complex molecular architectures.
1-(2-Bromo-4-methylphenyl)ethanone serves as a versatile building block in medicinal chemistry and synthetic organic research, enabling direct functionalization at the aromatic ring via palladium-catalyzed cross-coupling reactions. The ketone functionality offers a site for nucleophilic addition or enolization, while the bromo and methyl groups provide orthogonal handles for further diversification. Bench-stable and compatible with standard reaction conditions, it facilitates efficient construction of complex aryl-substituted scaffolds relevant to pharmaceutical development.
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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
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Precautionary Statements : P261-P302+P352
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Lot numbers can be found on the outside label of a product: