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Z-L-Ala-CHN2

Z-L-Ala-CHN2 is a protected L-alanine derivative in which the amino group is masked as a benzyloxycarbonyl (Z, Cbz) carbamate and the carboxyl functionality is converted to a diazomethyl amide (-CHN2), yielding an amino acid-based peptide intermediate. The molecule contains the stereogenic center associated with L-alanine, a carbamate-protected α-amino group, and a diazo group that provides a reactive handle for subsequent transformations while the carbonyls define the amide/carbamate framework. In synthesis and chemical biology workflows, Z-L-Ala-CHN2 is used as a building block for preparing substituted alanine derivatives and diazo-containing intermediates, including routes to labeled or functionalized amino acid analogues and related peptide or biomolecule conjugation precursors.

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

CAT No: CP25983

CAS No:67865-68-3

Synonyms/Alias:Pheneturide;Ethylphenacemide;2-Phenylbutyrylurea;Ethylphenylacetylurea;Benuride;Laburide;Lircapyl;Phenuride;90-49-3;d-Pheneturide;dl-Pheneturide;l-Pheneturide;Aethylphenacemidum;Urea,(2-phenylbutyryl)-;(+)-Pheneturide;(-)-Pheneturide;1-((Ethyl)phenylacetyl)urea;Phenylethylacetyluree;Urea,(2-phenylbutyryl)-,(+-)-;(2-phenylbutanoyl)urea;Pheneturide[INN:BAN];Feneturida[INN-Spanish];Pheneturidum[INN-Latin];N-(alpha-Phenylbutyryl)urea;S46

Chemical Name:N-alpha-Benzyloxycarbonyl-L-alainyl-diazomethane, (3S)-3-Z-amino-1-diazo-2-butanone

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M.F/Formula
C11H14N2O2
M.W/Mr.
247,26 g/mole
Size
1 g;
InChI
1S/C11H14N2O2/c1-2-9(10(14)13-11(12)15)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H3,12,13,14,15)
InChI Key
AJOQSQHYDOFIOX-UHFFFAOYSA-N
Canonical SMILES
CCC(C1=CC=CC=C1)C(=O)NC(=O)N

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