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Structure of 231958-14-8
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6-((tert-Butoxycarbonyl)amino)nicotinic acid features a protected amino group flanked by a pyridine ring, enabling selective deprotection in peptide synthesis. This bench-stable derivative facilitates the incorporation of functionalized nicotinic scaffolds into bioactive molecules under standard conditions.
6-((tert-Butoxycarbonyl)amino)nicotinic acid serves as a versatile building block in medicinal chemistry, enabling the selective introduction of a protected amino group at the 6-position of the nicotinic acid scaffold. The tert-butyl carbamate (Boc) moiety provides excellent bench stability and orthogonal deprotection compatibility, facilitating downstream functionalization via standard hydrogenolysis or acidic cleavage. Its well-defined reactivity supports efficient incorporation into peptide-like sequences and heterocyclic systems relevant to drug discovery 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: