N-Boc-gamma-aminobutyric Acid

• CAT Number: R035823
• CAS Number: 57294-38-9
• Molecular Formula: C9H17NO4
• Molecular Weight: 203.24
• Purity: ≥95%
• Synonyms: Boc-4-aminobutanoic Acid; N-Boc-4-Aminobutyric Acid; N-Boc-γ-aminobutyric Acid?N-tert-Butoxycarbonyl-γ-aminobutyric Acid; NSC 164040; 4-(tert-Butoxycarbonyl)aminobutyric Acid; 4-(tert-Butyloxycarbonylamino)butanoic Acid; 4-[(tert-Butoxycarbonyl)amino
• Target: PROTAC Linkers
• Storage: -20°C
• IUPAC Name: 4-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
• InChI: InChI=1S/C9H17NO4/c1-9(2,3)14-8(13)10-6-4-5-7(11)12/h4-6H2,1-3H3,(H,10,13)(H,11,12)
• InChIKey: HIDJWBGOQFTDLU-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NCCCC(=O)O

N-Boc-gamma-aminobutyric acid (Cat No.:R035823) is a protected derivative of gamma-aminobutyric acid, featuring a tert-butoxycarbonyl (Boc) group on the amino terminus. This protecting group enhances the compound’s stability and selectivity during peptide synthesis and other organic transformations. N-Boc-GABA is commonly used as a building block in the preparation of pharmaceuticals, neuroactive compounds, and peptidomimetics. The Boc group can be selectively removed under acidic conditions, allowing for controlled deprotection. Its structural properties make it a valuable intermediate in medicinal chemistry and the development of GABA-related bioactive molecules.