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Structure of 955395-98-9
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4-Chloro-2-methoxy-5-nitropyridine features a trifunctional pyridine core with complementary reactivity: the chlorine enables palladium-catalyzed cross-coupling, the methoxy group offers steric and electronic modulation, and the nitro substituent serves as a strong electron-withdrawing anchor for further functionalization. This scaffold integrates readily into complex heterocyclic architectures under standard conditions.
4-Chloro-2-methoxy-5-nitropyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloropyridine moiety. The methoxy and nitro groups provide orthogonal functional handles for selective derivatization, while the compound exhibits good bench stability and facilitates efficient purification. Its defined substitution pattern supports predictable reactivity in heterocyclic scaffold construction.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: