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Structure of 15862-31-4
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2-Amino-3-bromo-5-nitropyridine features a strategically positioned bromine atom and nitro group on a pyridine scaffold, enabling direct functionalization in cross-coupling reactions. The electron-deficient ring facilitates nucleophilic substitution, while the amino group offers a handle for further derivatization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and advanced pharmaceutical building blocks.
2-Amino-3-bromo-5-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its bromo group and compatible amino functionality. The nitro group provides a handle for selective reduction or further functionalization, while the molecule exhibits sufficient bench stability for routine handling. Its orthogonal reactivity profile facilitates the construction of complex pyridine-based scaffolds relevant to medicinal chemistry and agrochemical development.
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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: