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Z-D-Glu(OBzl)-OH

Z-D-Glu(OBzl)-OH is a protected, esterified derivative of the amino acid class glutamic acid, bearing a benzyloxycarbonyl (Z) protecting group on the α-amino functionality and a benzyl ester (OBzl) at the γ-carboxyl position while retaining the α-carboxylic acid as a free carboxyl group (-CO2H). The molecule therefore contains both an unprotected carboxyl group and protected carboxyl/amine functionalities, with stereochemistry indicated as D by the product name. Z-D-Glu(OBzl)-OH is used as a peptide-synthesis building block and intermediate in protected amino acid strategies, where the orthogonal protection pattern supports chemoselective coupling and subsequent deprotection steps to access glutamate-containing peptide fragments or more complex amino acid derivatives.

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

CAT No: CP27249

CAS No:59486-73-6

Synonyms/Alias:59410-82-1;(S)-Ethyl2-amino-2-phenylacetatehydrochloride;(S)-Ethyl2-amino-2-phenylacetateHCl;L-PhenylglycineEthylEsterHydrochloride;17609-48-2;H-Phg-OEtHCl;SCHEMBL1851016;CTK8B3294;MolPort-020-004-206;ANW-42220;AKOS015933063;l-phenylglycineethylesterhydrochloride;AK130683;KB-211710;ST2414660;TX-017674;FT-0698655;V6822;D/L-ALPHA-PHENYLGLYCINEETHYLESTERHYDROCHLORIDE;I01-10222;72651-17-3

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cGMP Peptide
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M.F/Formula
C10H14ClNO2
M.W/Mr.
371.39
Size
1 g;5 g;25 g;
InChI
1S/C10H13NO2.ClH/c1-2-13-10(12)9(11)8-6-4-3-5-7-8;/h3-7,9H,2,11H2,1H3;1H/t9-;/m0./s1
InChI Key
FNNXQLSKQSVNLL-FVGYRXGTSA-N
Canonical SMILES
CCOC(=O)C(C1=CC=CC=C1)N.Cl

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