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Structure of 4913-57-9
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2,6-Dimethyl-4-nitropyridine features a pyridine core with electron-withdrawing nitro and electron-donating methyl groups in strategic positions. This electronic asymmetry enhances its utility in metal coordination and as a building block for functionalized heterocycles. The sterically protected ring system ensures stability under standard conditions, enabling reliable use in synthetic transformations and catalytic applications.
2,6-Dimethyl-4-nitropyridine serves as a versatile building block in synthetic organic chemistry, enabling regioselective functionalization at the 3-position due to electronic deactivation at C2 and C6. Its nitro group facilitates subsequent reduction to an amine or participation in nucleophilic substitution reactions, while the methyl groups enhance stability and influence reactivity profiles. This compound functions effectively in heterocycle synthesis and is valued for its bench stability and compatibility with standard coupling protocols.
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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-H320-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: