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Structure of 6945-68-2
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2-Amino-5-bromo-3-nitropyridine features a trifunctional pyridine core with electron-withdrawing nitro and bromo groups flanking a nucleophilic amino substituent. This combination enables direct coupling reactions and facilitates regioselective functionalization in heterocyclic synthesis. The molecule exhibits bench-stable handling characteristics and integrates readily into complex molecular architectures under standard conditions.
2-Amino-5-bromo-3-nitropyridine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to functionalized pyridine scaffolds. The amino group facilitates nucleophilic substitution and coupling reactions, while the bromo and nitro functionalities provide orthogonal handles for cross-coupling and selective reduction. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for 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: