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Z-L-α-aminoadipic acid- d -t-butyl ester.DCHA

Z-L-α-aminoadipic acid- d -t-butyl ester.DCHA is a protected amino acid derivative based on L-α-aminoadipic acid, featuring a Z (benzyloxycarbonyl) carbamate protection on the amino group and a tert-butyl ester protecting the carboxyl functionality, with an additional DCHA counterion associated to the salt form. The molecule contains the protected carbamate and ester functionalities that mask the free amino and carboxyl groups while retaining the adipic acid-derived six-carbon backbone and its internal methylene chain for controlled chemical handling and subsequent deprotection. In peptide and amino acid chemistry workflows, it functions as a protected building block or intermediate for stepwise incorporation of the aminoadipic acid side chain into larger peptide derivatives and for preparing labeled or conjugatable amino acid frameworks under conditions that require chemoselective protection of the amino and carboxyl groups.

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

CAT No: CP02708

CAS No:201668-30-6

Synonyms/Alias:201668-30-6;Cbz-Aad(OtBu)-OH.DCHA;Z-AAD(OTBU)-OHDCHA;SCHEMBL1143900;C18H25NO6.C12H23N;Z5730;Z-L-a-aminoadipicacid-d-t-butylesterDCHA;K-5903

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M.F/Formula
C30H48N2O6
M.W/Mr.
532.7
Abbr
Cbz-Aad(OtBu)-OH.DCHA
InChI
1S/C18H25NO6.C12H23N/c1-18(2,3)25-15(20)11-7-10-14(16(21)22)19-17(23)24-12-13-8-5-4-6-9-13;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-6,8-9,14H,7,10-12H2,1-3H3,(H,19,23)(H,21,22);11-13H,1-10H2/t14-;/m0./s1
InChI Key
RYOMDXINFGAENM-UQKRIMTDSA-N
Canonical SMILES
CC(C)(C)OC(=O)CCCC(C(=O)O)NC(=O)OCC1=CC=CC=C1.C1CCC(CC1)NC2CCCCC2

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