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Structure of 171670-07-8
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This Boc-protected picolinic acid derivative features a strategically positioned amine handle for facile conjugation, enabling direct incorporation into peptide and small-molecule scaffolds. The tert-butoxycarbonyl group provides robust protection under standard reaction conditions, while the pyridine ring offers enhanced solubility and stability in polar solvents.
6-(((tert-Butoxycarbonyl)amino)methyl)picolinic acid serves as a versatile building block for the synthesis of bioactive heterocycles and peptide conjugates. The tert-butyl carbamate group provides excellent stability under basic conditions and facilitates selective deprotection during late-stage functionalization. Its pendant picolinic acid moiety enables direct coupling reactions, while the benzylic amine functionality supports orthogonal derivatization in multi-step syntheses. Functions reliably in standard SPPS and solution-phase 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: