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Z-L-aspartic acid β-allyl ester

Z-L-aspartic acid β-allyl ester is an L-aspartate-derived amino acid ester in which the α-carboxyl group is masked as a β-allyl ester while the side chain retains the aspartic acid β-carboxyl functionality as an esterified substituent, and the amino functionality is present as a Z-protected (benzyloxycarbonyl) group. The molecule bears a carbamate protecting group on the nitrogen (Z), and the β-allyl ester provides an allyl ester handle that can be manipulated under conditions suited to ester deprotection or allyl group transformations, while the stereochemistry is specified as L by the product name. In peptide and amino acid chemistry workflows, this protected ester form is employed as a controlled-release building block for preparing aspartate-containing intermediates and for accessing selectively functionalized aspartyl derivatives in solution-phase or solid-phase synthesis and in structure-activity or labeling studies requiring an aspartate side-chain ester.

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

CAT No: CP00432

CAS No:99793-10-9

Synonyms/Alias:99793-10-9;AmbotzZAA1042;Z-Asp(OAll)-OH;Z-L-asparticacidss-allylester;ZINC94568742;X5760;A-9315;N-(Benzyloxycarbonyl)-L-asparticacid4-allylester;L-Asparticacid,N-[(phenylmethoxy)carbonyl]-,4-(2-propen-1-yl)ester

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M.F/Formula
C15H17NO6
M.W/Mr.
307.3
Abbr
Z-Asp(OAll)-OH
InChI
1S/C15H17NO6/c1-2-8-21-13(17)9-12(14(18)19)16-15(20)22-10-11-6-4-3-5-7-11/h2-7,12H,1,8-10H2,(H,16,20)(H,18,19)/t12-/m0/s1
InChI Key
LKXLDZQGKGEICY-LBPRGKRZSA-N
Canonical SMILES
C=CCOC(=O)CC(C(=O)O)NC(=O)OCC1=CC=CC=C1

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