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Structure of 31984-10-8
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1-Bromo-4-phenylbutan-2-one features a bromine atom at the terminal position of a butanone chain flanked by a phenyl group and a ketone. This electrophilic site enables efficient coupling in C–C bond formation, while the aryl substituent enhances stability and modulates reactivity. The molecule serves as a key intermediate in synthesizing functionalized alkylated aromatics and complex heterocycles under standard conditions.
1-Bromo-4-phenylbutan-2-one serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted cyclohexanes and heterocyclic systems via Michael addition and cyclization cascades. Its α-bromoketone functionality facilitates nucleophilic substitution and enolate formation under mild conditions, while the phenyl group enhances stability and provides a handle for further functionalization. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis in medicinal chemistry and process 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: