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Structure of 5326-87-4
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2-Bromo-N-phenylacetamide features a bromine atom at the alpha position relative to the amide carbonyl, enhancing its reactivity in nucleophilic substitution and coupling processes. This bench-stable compound integrates readily into synthetic sequences requiring electrophilic functionality, particularly in the construction of aryl-substituted heterocycles and bioactive intermediates.
2-Bromo-N-phenylacetamide serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted anilines and heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. Its bromo group facilitates reliable C–C and C–N bond formation under standard coupling conditions, while the amide functionality provides stability and compatibility with diverse reaction environments. The compound exhibits excellent bench stability and is readily purified by recrystallization, 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 : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: