Z-D-Ala-OSu

Z-D-Ala-OSu is a protected D-alanine derivative in which the amino group is carbamated with a benzyloxycarbonyl (Z, Cbz) protecting group and the carboxyl functionality is converted to an N-hydroxysuccinimide (OSu) ester. The molecule contains a Z-protected amino group and a carboxyl-derived OSu ester, with stereochemistry specified as D at the alanine center and a side chain consisting of a methyl group, while the OSu ester bears a leaving group suited to acyl transfer chemistry. Z-D-Ala-OSu is used in peptide and amide bond synthesis as an activated amino acid acylating agent, and it also serves as a reagent for preparing labeled or conjugated alanine-containing derivatives under conditions that promote nucleophilic acyl substitution.

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

CAT No: CP26930

CAS No:27167-53-9

Synonyms/Alias:Z-D-Ala-OSu;27167-53-9;AC1LHGYH;SCHEMBL10345811;CTK8G3817;MolPort-020-004-595;ZINC365049;Z-D-alanine-N-hydroxysuccinimideester;AK-81316;K-6940;(2,5-dioxopyrrolidin-1-yl)(2R)-2-(phenylmethoxycarbonylamino)propanoate;1-[(R)-1-Oxo-2-[[(benzyloxy)carbonyl]amino]propoxy]-2,5-pyrrolidinedione;D-Alanine,N-[(phenylmethoxy)carbonyl]-,2,5-dioxo-1-pyrrolidinylester

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M.F/Formula
C15H16N2O6
M.W/Mr.
320.3
Size
5 g;25 g;
InChI
1S/C15H16N2O6/c1-10(14(20)23-17-12(18)7-8-13(17)19)16-15(21)22-9-11-5-3-2-4-6-11/h2-6,10H,7-9H2,1H3,(H,16,21)/t10-/m1/s1
InChI Key
OFIYNISEFIEQBC-SNVBAGLBSA-N
Canonical SMILES
CC(C(=O)ON1C(=O)CCC1=O)NC(=O)OCC2=CC=CC=C2

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