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Structure of 337904-92-4
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5-((tert-Butoxycarbonyl)amino)nicotinic acid features a protected amino group flanked by a pyridine ring, enabling selective functionalization in peptide and heterocyclic synthesis. This bench-stable derivative facilitates efficient incorporation into complex molecular architectures under standard conditions.
5-((tert-Butoxycarbonyl)amino)nicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and peptide conjugates. The tert-butyl carbamate (Boc) group provides excellent stability under basic conditions and facilitates straightforward deprotection during late-stage functionalization. Its pyridine carboxylic acid scaffold supports diverse coupling reactions, including amide formation and transition-metal-catalyzed cross-couplings, making it well-suited for scalable 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: