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Structure of 160590-36-3
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2-Methoxy-4-methyl-3-nitropyridine features a nitro group at C3, flanked by electron-donating methoxy and methyl substituents, creating a uniquely polarized heterocyclic framework. This arrangement enhances regioselective reactivity in cross-coupling and nucleophilic substitution processes, enabling efficient incorporation into functionalized pharmaceutical intermediates and advanced materials.
2-Methoxy-4-methyl-3-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via selective reduction and coupling reactions. Its orthogonal functional groups—nitro, methoxy, and methyl—support sequential transformations under mild conditions, facilitating the construction of complex nitrogen-containing architectures relevant to medicinal chemistry. The compound exhibits good bench stability and is amenable to purification by standard chromatographic techniques.
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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: