N-δ-Boc-L-ornithine is a protected, proteinogenic amino acid derivative in which the δ-amino group of L-ornithine is carbamated with a Boc (tert-butoxycarbonyl) protecting group, yielding a side-chain-protected basic amino acid. The molecule retains the free α-amino and α-carboxyl functional groups while converting the side-chain primary amine into a Boc-protected carbamate, and its stereochemistry corresponds to the L-configuration indicated in the name. N-δ-Boc-L-ornithine is used as a building block for stepwise peptide synthesis and for preparing ornithine-containing peptide analogues or conjugates where selective control of the side-chain amine is required during coupling and subsequent deprotection.
CAT No: CP08729
CAS No:13650-49-2
Synonyms/Alias:13650-49-2;H-Orn(Boc)-OH;N-delta-Boc-L-Ornithine;(S)-2-Amino-5-((tert-butoxycarbonyl)amino)pentanoicacid;(2S)-2-amino-5-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoicacid;N-alpha-t-BOC-L-ORNITHINE;AmbotzHAA1168;N-d-Boc-L-ornithine;Ndelta-Boc-L-ornithine;AC1ODTN8;(S)-2-AMINO-5-TERT-BUTOXYCARBONYLAMINO-PENTANOICACID;SCHEMBL7195305;CHEMBL1222173;CTK8G1721;GLZZMUULAVZVTA-ZETCQYMHSA-N;MolPort-008-267-977;ZINC1640080;MFCD00037219;AKOS015998751;AM82629;CS18712;N(delta)-t-butyloxycarbonyl-L-ornithine;AJ-28563;AK-49367;SC-10411
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