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Structure of 2897-43-0
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2,6-Dichloro-3-nitropyridin-4-amine features a pyridine core bearing two chlorine substituents and a nitro group at C3, with an amine functionality at C4. This electron-deficient heterocycle integrates readily into cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive nitrogen-containing compounds.
2,6-Dichloro-3-nitropyridin-4-amine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via nucleophilic displacement and subsequent reduction. The dichloro substitution pattern facilitates sequential functionalization, while the nitro and amino groups provide orthogonal reactivity for downstream transformations. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for medicinal chemistry campaigns and process-scale applications.
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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: