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Structure of 37660-64-3
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4,6-Dichloro-3-nitropyridin-2-amine features a pyridine core bearing two chlorine substituents and a nitro group at the 3-position, enabling high reactivity in cross-coupling and nucleophilic substitution reactions. The electron-deficient ring facilitates efficient coupling with amines and heterocycles under mild conditions. This bench-stable compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals.
4,6-Dichloro-3-nitropyridin-2-amine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The dichloro pattern facilitates sequential functionalization, while the nitro and amino groups offer orthogonal reactivity for downstream transformations. Bench-stable and readily purified, it supports scalable synthesis of pharmaceutical intermediates and agrochemicals.
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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: