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Z-D-2-Nal-OH

Z-D-2-Nal-OH is a protected, deuterated? (not indicated) Actually "Z" indicates a benzyloxycarbonyl-type protection? Here "Z" commonly denotes the Cbz (benzyloxycarbonyl) protecting group, and "D-2-Nal-OH" indicates the D stereoisomer of 2-naphthylalanine bearing a free carboxylic acid. The molecule contains a Cbz (Z) carbamate-protected amino group and an unprotected carboxyl group, with a 2-naphthyl side chain that provides a hydrophobic, aromatic functionality for incorporation into peptide-like structures. Z-D-2-Nal-OH is used as a protected amino acid building block for peptide synthesis and as a structural probe in chemical biology and protein-structure studies where an aromatic naphthyl side chain is introduced at defined positions.

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

CAT No: CP26378

CAS No:143218-10-4

Synonyms/Alias:143218-10-4;Z-D-2-Nal-OH;(R)-2-(((Benzyloxy)carbonyl)amino)-3-(naphthalen-2-yl)propanoicacid;Z-3-(2-naphthyl)-D-alanine;Cbz-3-(2-Naphthyl)-D-alanine;Cbz-3--D-alanine;96828_ALDRICH;Z-3-(1-naphthyl)-L-alanine;96828_FLUKA;CTK8G3805;MolPort-003-939-969;ZINC2555633;6524AH;CZ-141;AKOS015911017;AK163590;FT-0643358;ST24035217;I14-39012;(2R)-2-{[(benzyloxy)carbonyl]amino}-3-naphthalen-2-ylpropanoicacid

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M.F/Formula
C21H19NO4
M.W/Mr.
349.39
Size
1 g;5 g;
InChI
1S/C21H19NO4/c23-20(24)19(22-21(25)26-14-15-6-2-1-3-7-15)13-16-10-11-17-8-4-5-9-18(17)12-16/h1-12,19H,13-14H2,(H,22,25)(H,23,24)/t19-/m1/s1
InChI Key
XBRPIBMAJOTVHG-LJQANCHMSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CC2=CC3=CC=CC=C3C=C2)C(=O)O

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