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Structure of 79839-29-5
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This chiral azepane-containing amino acid derivative features a protected amine and carboxylic acid functional group, enabling direct incorporation into peptide synthesis workflows. The tert-butyl carbamate moiety provides stability and orthogonal protection, while the (S)-configuration ensures stereochemical fidelity in downstream conjugation.
(S)-2-(3-((tert-butoxycarbonyl)amino)-2-oxoazepan-1-yl)acetic acid serves as a versatile chiral building block for the synthesis of bioactive azepane-containing scaffolds. The protected amine and carboxylic acid functionalities enable orthogonal functionalization, while the tert-butyl carbamate group ensures bench stability and compatibility with standard peptide coupling protocols. This compound facilitates efficient access to complex heterocyclic systems via established cyclization and deprotection sequences.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: