Z-L-Pip-OH is a protected amino acid derivative featuring L-pipecolic acid (L-Pip) in which the amino functionality is masked by a benzyloxycarbonyl (Z, Cbz) protecting group, while the molecule retains a free carboxylic acid (-COOH) for subsequent coupling chemistry. The structure therefore presents a Cα stereocenter consistent with the L designation and a saturated six-membered ring side chain (pipecolate) bearing a secondary amine-free cyclic framework, with the Z carbamate controlling chemoselectivity by preventing unprotected amine reactivity during peptide or amide bond formation. Z-L-Pip-OH is used as a building block for stepwise peptide synthesis and for preparing more complex amino acid and peptide derivatives where controlled protection of the amino group supports sequential functionalization and purification by standard organic chemistry workflows.
CAT No: CP25707
CAS No:28697-09-8
Synonyms/Alias:28697-09-8;(R)-1-((Benzyloxy)carbonyl)piperidine-2-carboxylicacid;(R)-(+)-1-Cbz-2-piperidinecarboxylicacid;N-Cbz-(R)-(+)-pipecolinicacid;(D)-N-(BENZYLOXYCARBONYL)PIPECOLICACID;(D)-N-CBZ-PIPECOLICACID;(R)-1-(Benzyloxycarbonyl)-2-piperidinecarboxylicAcid;(R)-1-CBZ-PIPERIDINE-2-CARBOXYLICACID;(2R)-1-[(BENZYLOXY)CARBONYL]PIPERIDINE-2-CARBOXYLICACID;AmbotzZAA1005;PubChem6270;AC1LELW3;Z-L-PIP-OH;AC1Q71DO;AC1Q71DP;SCHEMBL82714;1,2-Piperidinedicarboxylicacid,1-(phenylmethyl)ester,(2R)-;516376_ALDRICH;N-Carbobenzoxy-D-pipecolicAcid;N-CBZ-D-PIPECOLINICACID;CTK4G1935;ZINC57123;MolPort-001-794-620;ZSAIHAKADPJIGN-GFCCVEGCSA-N;AKOS010366802
Chemical Name:(R)-(+)-N-Benzyloxycarbonyl-pipecolinic acid
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