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Structure of 473924-63-9
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This pyridine-based scaffold features a tert-butoxycarbonyl-protected amine and a carboxylic acid group, enabling orthogonal functionalization. The molecule integrates seamlessly into peptide coupling workflows and serves as a key intermediate for bioactive compound synthesis under standard bench conditions.
2-({[(tert-Butoxy)carbonyl]amino}methyl)pyridine-4-carboxylic acid serves as a versatile building block for pyridine-based pharmacophores, enabling efficient access to bioactive scaffolds via orthogonal deprotection. The tert-butyl carbamate (Boc) group ensures stability and compatibility with standard coupling reactions, while the carboxylic acid facilitates amide bond formation. Its dual functionality supports modular synthesis of heterocyclic compounds in medicinal chemistry 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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: