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Structure of 10409-54-8
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2-Bromo-2-methyl-1-phenylpropan-1-one features a brominated ketone scaffold that enables direct incorporation into C–C bond formation strategies. The α-bromoketone functionality supports nucleophilic substitution and enolate chemistry under mild conditions, offering reliable access to complex alkylated derivatives in synthetic organic workflows.
2-Bromo-2-methyl-1-phenylpropan-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient access to quaternary carbon centers via nucleophilic substitution or conjugate addition. Its α-bromoketone functionality facilitates C–C bond formation under mild conditions, with high bench stability and compatibility across diverse reaction environments. The molecule functions effectively in the synthesis of complex heterocycles and pharmaceutical intermediates, offering predictable reactivity and straightforward purification.
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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: