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Structure of 33225-73-9
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6-Nitronicotinic acid features a nitro group positioned at the 6-position of the nicotinic acid scaffold, imparting strong electron-withdrawing character. This configuration enhances acidity and influences reactivity in electrophilic substitution and coupling processes. The molecule integrates readily into bioactive heterocycles and serves as a key intermediate in pharmaceutical synthesis under standard conditions.
6-Nitronicotinic acid serves as a versatile building block in heterocyclic synthesis, enabling direct access to nitro-substituted pyridine scaffolds relevant to medicinal chemistry and agrochemical development. Its ortho-nitro functionality facilitates subsequent transformations such as reduction to amino derivatives or metal-catalyzed cross-couplings. The compound exhibits good bench stability and is readily purified by recrystallization, supporting its use in multi-step synthetic sequences requiring functional group compatibility and predictable reactivity.
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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: