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Z-4-phenyl-D-Phe-OH

Z-4-phenyl-D-Phe-OH contains a benzyl-type Z-protecting group on the amino acid nitrogen and a 4-phenyl-substituted phenylalanine skeleton, classifying it as a protected, nonstandard amino acid derivative rather than a free natural amino acid. The molecule bears both an amino functionality (masked by the Z group) and a carboxylic acid (-COOH) for further coupling, with the D stereochemical form indicated by the name and a side chain featuring a substituted phenyl ring that provides hydrophobic and aromatic character. It is used as a protected amino acid building block for peptide synthesis and related structure-activity or labeling studies where a D-configured, aryl-substituted phenylalanine residue is incorporated into larger peptide or amino acid derivative frameworks.

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

CAT No: CP26536

CAS No:176794-80-2

Synonyms/Alias:176794-80-2;CBZ-4-BIPHENYL-D-ALA;Z-D-Ala(4,4'-bipheyl)-OH;SCHEMBL14509085;CTK8E9912;MolPort-020-004-221;ZINC2389775;AKOS015909215;AJ-35617;AK-60100;AM002366;RT-016302;FT-0643710;K-5425;Z-beta-(4-biphenylyl)-D-Ala-OH,Z-D-Bip-OH;I14-33230;(2R)-2-{[(BENZYLOXY)CARBONYL]AMINO}-3-{[1,1'-BIPHENYL]-4-YL}PROPANOICACID;(R)-3-([1,1'-Biphenyl]-4-yl)-2-(((benzyloxy)carbonyl)amino)propanoicacid

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M.F/Formula
C23H21NO4
M.W/Mr.
375.42
Size
1 g;5 g;
InChI
1S/C23H21NO4/c25-22(26)21(24-23(27)28-16-18-7-3-1-4-8-18)15-17-11-13-20(14-12-17)19-9-5-2-6-10-19/h1-14,21H,15-16H2,(H,24,27)(H,25,26)/t21-/m1/s1
InChI Key
ZZIBVIHXEMIHEQ-OAQYLSRUSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CC2=CC=C(C=C2)C3=CC=CC=C3)C(=O)O

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