Z-Orn(Z)-OSu

Z-Orn(Z)-OSu is an N-protected ornithine derivative in which the α-amino group is carbobenzyloxy-protected (Z) and the side-chain ω-amino group is also protected as a benzyloxycarbonyl (Z), forming a bis-Z ornithine framework. The molecule terminates in an activated N-hydroxysuccinimide ester (OSu) at the carboxylate position, while retaining the two protected amine functionalities that modulate chemoselectivity and suppress unprotected nucleophilic side reactions. As an amino acid activated ester, Z-Orn(Z)-OSu is employed as a precursor for peptide and amide bond formation in solution-phase synthesis and for preparing ornithine-containing peptide derivatives under conditions where the OSu leaving group enables coupling to amines.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: CP27581

CAS No:90970-61-9

Synonyms/Alias:Z-ORN(Z)-OSU;90970-61-9;Z-ORN-OSU;SCHEMBL8613001;C25H27N3O8;7949AH;KM2952;ZINC71788230;BP-11082

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M.F/Formula
C25H27N3O8
M.W/Mr.
497.51
Size
5 g;25 g;
InChI
1S/C25H27N3O8/c29-21-13-14-22(30)28(21)36-23(31)20(27-25(33)35-17-19-10-5-2-6-11-19)12-7-15-26-24(32)34-16-18-8-3-1-4-9-18/h1-6,8-11,20H,7,12-17H2,(H,26,32)(H,27,33)/t20-/m0/s1
InChI Key
PGMBMJCWSOQENR-FQEVSTJZSA-N
Canonical SMILES
C1CC(=O)N(C1=O)OC(=O)C(CCCNC(=O)OCC2=CC=CC=C2)NC(=O)OCC3=CC=CC=C3

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