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Structure of 4487-50-7
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2-Amino-4-nitropyridine features a strategically positioned amino group flanked by a nitro substituent on the pyridine ring, creating a potent electron-deficient heterocycle. This combination enables direct incorporation into transition-metal-catalyzed cross-coupling reactions and facilitates rapid derivatization in medicinal chemistry campaigns. The molecule exhibits enhanced solubility in polar solvents and stability under standard bench conditions.
2-Amino-4-nitropyridine serves as a versatile building block in medicinal chemistry, enabling efficient access to nitrogen-containing heterocycles through directed functionalization. Its ortho-amino and nitro groups facilitate sequential transformations, including reduction, coupling, and cyclization reactions, with excellent bench stability and straightforward purification. This compound functions as a key intermediate in the synthesis of pyridine-based API scaffolds and bioactive molecules.
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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: