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Structure of 77611-37-1
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This chiral building block features a protected amine and a hydroxyl group flanking a six-carbon chain, enabling direct incorporation into peptide architectures. The tert-butyl carbamate handle ensures orthogonal deprotection, while the pendant hydroxy function offers a site for selective derivatization or glycosylation.
(S)-2-((tert-Butoxycarbonyl)amino)-6-hydroxyhexanoic acid serves as a versatile chiral building block for peptide and heterocyclic synthesis, enabling efficient access to bioactive scaffolds. The protected amine and terminal hydroxyl group provide orthogonal functionality for sequential derivatization, while the tert-butoxycarbonyl (Boc) group ensures bench stability and compatibility with standard coupling protocols. Its structure facilitates straightforward purification and integration into multi-step syntheses of complex molecules.
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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: