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Structure of 353281-15-9
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2-Chloro-3-nitroisonicotinic acid features a strategically positioned chloro group and electron-deficient nitro moiety on the pyridine ring, enabling direct incorporation into heterocyclic scaffolds. This bench-stable derivative delivers enhanced reactivity in cross-coupling and cyclization processes under standard conditions.
2-Chloro-3-nitroisonicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted isonicotinamide scaffolds through amide coupling or nucleophilic displacement. Its ortho-chloro and meta-nitro groups provide complementary reactivity for sequential functionalization, with good bench stability and straightforward purification via recrystallization. The molecule functions effectively in standard cross-coupling and heterocycle formation protocols, offering reliable access to bioactive intermediates in 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: