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Structure of 6332-56-5
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3-Nitropyridin-2(1H)-one features a pyridinone core bearing a nitro group at the 3-position, conferring enhanced electron-withdrawing character. This arrangement supports its use in transition metal-catalyzed cross-coupling reactions and as a building block for bioactive heterocycles. The compound exhibits bench-stable handling under standard conditions.
3-Nitropyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling the construction of nitrogen-rich heterocyclic scaffolds. Its dual functionality—pyridinone and nitro groups—facilitates selective transformations, including reduction to amino derivatives and coupling reactions under standard conditions. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it valuable for iterative 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: