γ-Aminobutyric acid benzyl ester p-tosylate is an amino acid ester derivative of γ-aminobutyric acid in which the carboxyl group is converted to a benzyl ester and the amino functionality is present as a p-tosylate (tosyl-protected amine). The molecule therefore contains an ester carbonyl linked to a benzyl group, while the N-terminus bears a p-toluenesulfonyl protecting group that reduces free amine nucleophilicity and helps control chemoselective transformations. This protected ester/amine building block is used in peptide and amino acid derivative synthesis to support stepwise coupling and to manage orthogonal reactivity of the protected γ-aminobutyric acid side.
CAT No: CP02803
CAS No:26727-22-0
Synonyms/Alias:Benzyl4-aminobutanoate4-methylbenzenesulfonate;26727-22-0;H?-Abu-OBzl.p-tosylate;HGamma-Abu-OBzl.p-tosylate;C18H23NO5S;SCHEMBL1363911;CTK8B7671;AVEADJJUOBFQIQ-UHFFFAOYSA-N;MolPort-000-740-043;2415AB;ANW-58117;AKOS016002989;MCULE-9399058680;AK-87747;OR070380;TC-146862;ST24046114;BENZYL4-AMINOBUTANOATE;TOLUENESULFONICACID;J-300321;4-amino-butyricacidbenzylestertoluene-4-sulfonicacid
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