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Structure of 881-50-5
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N-(4-Bromo-2-nitrophenyl)acetamide features a brominated, electron-deficient aromatic ring paired with a reactive acetamide group, enabling direct incorporation into cross-coupling and heterocyclic synthesis. This bench-stable scaffold facilitates rapid access to functionalized biaryls and nitrogen-containing heterocycles under standard conditions.
N-(4-Bromo-2-nitrophenyl)acetamide serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted anilines and heterocyclic scaffolds. The bromo and nitro groups provide orthogonal handles for palladium-catalyzed cross-coupling and selective reduction, respectively. Its bench-stable nature and compatibility with standard functional group transformations facilitate reliable synthesis of complex intermediates in API 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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: