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Structure of 2483-46-7
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(S)-2,6-Bis((tert-butoxycarbonyl)amino)hexanoic acid serves as a key chiral building block for peptide synthesis, featuring two protected amine groups flanking a central aliphatic chain. The tert-butyl carbamate (Boc) moieties provide robust protection under acidic conditions while maintaining stability during coupling reactions. This bifunctional structure enables precise incorporation into complex peptide architectures, particularly in the design of cyclic or branched sequences where orthogonal protection is required.
(S)-2,6-Bis((tert-butoxycarbonyl)amino)hexanoic acid serves as a valuable chiral building block for the synthesis of peptide-based scaffolds and cyclic heterocycles. The molecule enables efficient construction of dipeptide mimetics and side-chain functionalized analogs through orthogonal deprotection strategies. Its tert-butyl carbamate groups provide excellent stability under standard reaction conditions and facilitate selective activation, purification, and downstream derivatization in multi-step syntheses.
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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: