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Z-2-Nal-OH

Z-2-Nal-OH contains the amino acid side-chain motif of 2-naphthylalanine (2-Nal) in a free carboxylic acid form, where the N-terminus is protected as a Z (benzyloxycarbonyl, Cbz) carbamate. The molecule bears both an amino group (as the carbamate-protected nitrogen) and a carboxylic acid, while the 2-naphthyl side chain provides a hydrophobic aromatic functionality for incorporation into peptide frameworks. Z-2-Nal-OH is employed as a protected amino acid building block for stepwise peptide synthesis and for structure-activity or binding studies that require an aromatic, non-proteinogenic amino acid residue with a controlled N-protection state.

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

CAT No: CP27328

CAS No:65365-16-4

Synonyms/Alias:Z-2-Nal-OH;65365-16-4;AC1ODZXP;Z-L-2-Nal-OH;SCHEMBL4634963;MolPort-003-990-213;XBRPIBMAJOTVHG-IBGZPJMESA-N;ZINC2597008;7847AH;KM0922;AKOS025289401;AK170129;N-(benzyloxycarbonyl)-3-(2-naphthyl)-L-alanine;(2S)-3-naphthalen-2-yl-2-(phenylmethoxycarbonylamino)propanoicacid;(2S)-2-{[(benzyloxy)carbonyl]amino}-3-naphthalen-2-ylpropanoicacid;2-Naphthalenepropanoicacid,a-[[(phenylmethoxy)carbonyl]amino]-,(aS)-

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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-/m0/s1
InChI Key
XBRPIBMAJOTVHG-IBGZPJMESA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CC2=CC3=CC=CC=C3C=C2)C(=O)O

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