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Structure of 2142-63-4
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3'-Bromoacetophenone features a brominated aryl ring coupled to a ketone functional group, enabling direct incorporation into cross-coupling and electrophilic substitution reactions. This bench-stable compound serves as a key intermediate in synthesizing bioactive molecules and advanced materials.
3'-Bromoacetophenone serves as a versatile building block in cross-coupling reactions and heterocycle synthesis, offering reliable functional group tolerance and bench stability. Its bromo substituent enables palladium-catalyzed coupling with boronic acids or amines, while the ketone moiety supports enolization, nucleophilic addition, and subsequent derivatization. This compound facilitates efficient access to substituted biaryl and aryl ketone scaffolds commonly found in medicinal chemistry campaigns.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: