Phthaloyl-glycine tert.butyl ester is a glycine-based amino acid derivative in which the amino group is acylated with a phthaloyl (phthalimide-like) protecting group and the carboxyl group is esterified as a tert-butyl ester. The molecule therefore bears a protected α-amino functionality, a tert-butyl ester carbonyl, and the phthaloyl aromatic imide/amide carbonyl system, with the side chain remaining as the glycine methylene unit. In peptide and amino acid chemistry workflows, this protected ester format functions as a stable intermediate that can be handled for stepwise assembly or further derivatization, while the phthaloyl group and tert-butyl ester provide chemoselective control over subsequent deprotection and coupling steps.
CAT No: CP00909
CAS No:6297-93-4
Synonyms/Alias:DL-Methionineethylesterhydrochloride;6297-53-6;SBB000541;C7H15NO2S.HCl;H-DL-Met-OEt.HCl;H-MET-OETHCL;L-Methionine,hydrochloride;ethylDL-methionatehydrochloride;SCHEMBL2031642;CTK8F9301;MolPort-002-497-762;NSC46033;6640AH;NSC-46033;NSC401038;NSC401317;AKOS025116608;MCULE-9963255300;NSC-401038;NSC-401317;AK187134;AM004628;SC-09762;ethyl2-amino-4-methylthiobutanoate,chloride;A819711
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