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Structure of 179056-94-1
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2-Chloro-4-methoxy-6-methyl-3-nitropyridine features a nitro group at C3 and a chloro substituent at C2, enabling efficient coupling in cross-coupling reactions. The methoxy and methyl groups enhance solubility and electronic modulation, while the pyridine core offers stability under standard conditions. This compound serves as a key intermediate in medicinal chemistry for constructing nitrogen-rich heterocycles.
2-Chloro-4-methoxy-6-methyl-3-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloropyridine moiety. The methoxy and methyl groups provide steric and electronic modulation, enhancing regioselectivity in subsequent transformations. Its bench-stable nature and compatibility with common protecting group strategies facilitate efficient access to complex pyridine-based scaffolds for medicinal chemistry and agrochemical development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: