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Structure of 850663-54-6
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4-Chloro-5-nitropyridin-2(1H)-one features a fused pyridinone core with complementary electron-withdrawing chlorine and nitro substituents, enabling selective functionalization in late-stage diversification. This bench-stable scaffold integrates readily into heterocyclic architectures via nucleophilic substitution or cross-coupling protocols under standard conditions.
4-Chloro-5-nitropyridin-2(1H)-one serves as a versatile building block in heterocyclic synthesis, enabling nucleophilic substitution at the C4 chloro position under mild conditions. The nitro group at C5 enhances electrophilicity and supports downstream transformations, including reduction to an amino derivative or participation in coupling reactions. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and API 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-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: