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Structure of 24484-96-6
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2-Amino-4-chloro-5-nitropyridine features a fused heterocyclic core bearing complementary reactive handles: a nucleophilic amino group, a chloro substituent for cross-coupling, and a strongly electron-withdrawing nitro group. This combination enables strategic functionalization in synthetic sequences requiring regioselective derivatization under mild conditions.
2-Amino-4-chloro-5-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling selective functionalization at multiple positions. Its amino and nitro groups provide orthogonal reactivity for sequential transformations, while the chlorine atom facilitates palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for medicinal chemistry campaigns and API intermediate development.
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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: