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Z-L-aspartic acid β-benzyl ester

Z-L-aspartic acid β-benzyl ester is a protected L-aspartic acid derivative in which the α-amino group is carbobenzyloxy (Z, benzyloxycarbonyl) protected and the side-chain carboxyl group is esterified as a β-benzyl ester, giving an aspartate scaffold with two carboxyl-related functionalities masked as protecting groups. The molecule contains a Z-protected amino functionality and a benzyl ester that together reduce free zwitterionic character and modulate chemoselectivity by preventing side reactions associated with unprotected amine and carboxyl groups. It is used as an amino acid building block or intermediate for peptide synthesis and related derivatization workflows where controlled exposure of the reactive termini is required for stepwise coupling and subsequent deprotection strategies.

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

CAT No: CP00433

CAS No:3479-47-8

Synonyms/Alias:Z-Asp(OBzl)-OH;3479-47-8;Cbz-Asp(OBzl)-OH;Z-L-asparticacid4-benzylester;(S)-4-(Benzyloxy)-2-(((benzyloxy)carbonyl)amino)-4-oxobutanoicacid;N-Cbz-L-asparticAcid4-BenzylEster;ST50826272;N-Benzyloxycarbonyl-L-AsparticAcid4-BenzylEster;N-Cbz-L-asparticacidbeta-benzylester;PubChem14963;AC1L2IDI;4-BenzylN-Cbz-L-aspartate;95980_ALDRICH;SCHEMBL7583002;95980_FLUKA;CTK3J6577;MolPort-003-939-906;ZINC1708468;EINECS222-456-1;4-BenzylN-Carbobenzoxy-L-aspartate;ANW-43243;CZ-028;MFCD00037820;AKOS015924111;MCULE-1611792115

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M.F/Formula
C19H19NO6
M.W/Mr.
357.4
Abbr
Z-Asp(OBzl)-OH
InChI
1S/C19H19NO6/c21-17(25-12-14-7-3-1-4-8-14)11-16(18(22)23)20-19(24)26-13-15-9-5-2-6-10-15/h1-10,16H,11-13H2,(H,20,24)(H,22,23)/t16-/m0/s1
InChI Key
VUKCNAATVIWRTF-INIZCTEOSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)CC(C(=O)O)NC(=O)OCC2=CC=CC=C2

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