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Structure of 56057-19-3
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6-Chloro-5-nitro-2-picoline features a chlorinated pyridine core with complementary nitro and methyl substituents, enabling direct incorporation into heterocyclic scaffolds. The electron-deficient aromatic ring facilitates nucleophilic substitution reactions under mild conditions, while the para-oriented nitro group enhances reactivity in cross-coupling processes. This bench-stable compound serves as a key intermediate for advanced pharmaceutical and agrochemical synthesis.
6-Chloro-5-nitro-2-picoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the pyridine ring due to orthogonal reactivity of the chloro and nitro groups. The chloro substituent facilitates palladium-catalyzed cross-coupling reactions, while the nitro group supports subsequent reduction to an amino moiety, offering access to diverse heterocyclic scaffolds. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthesis workflows.
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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: