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Structure of 105884-19-3
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1-(5-Bromo-2-chlorophenyl)ethanone features a brominated and chlorinated aromatic core paired with a reactive ketone group, enabling direct incorporation into cross-coupling reactions. This bench-stable compound serves as a key intermediate for synthesizing bioactive molecules in medicinal chemistry and materials science.
1-(5-Bromo-2-chlorophenyl)ethanone serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient construction of biologically relevant scaffolds. Its bromo and chloro substituents provide orthogonal handles for palladium-catalyzed cross-coupling reactions, while the acetyl group facilitates nucleophilic addition and condensation processes. The compound exhibits excellent bench stability and is compatible with standard purification methods, making it well-suited for scalable synthesis 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: