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Structure of 179024-65-8
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3-((tert-Butoxycarbonyl)amino)isonicotinic acid features a protected primary amine at the 3-position of a pyridine ring, enabling selective functionalization in peptide and heterocyclic synthesis. The tert-butyl carbamate group provides stability under standard conditions while allowing facile removal via mild acid treatment. This derivative serves as a key building block for bioactive molecule construction.
3-((tert-Butoxycarbonyl)amino)isonicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and peptide conjugates. The Boc-protected amine facilitates orthogonal functionalization, while the pyridine carboxylic acid moiety supports diverse coupling reactions. Its bench-stable nature and compatibility with standard purification protocols make it ideal for iterative synthetic workflows 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: