(2R)-2-[(Tert-butoxy)carbonylamino]-2-(4-bromophenyl)acetic acid

• CAT Number: L018074
• CAS Number: 1228570-47-5
• Molecular Formula: C13H16BrNO4
• Molecular Weight: 330.17
• Purity: ≥95%
• IUPAC Name: (2R)-2-(4-bromophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]acetic acid
• InChI: InChI=1S/C13H16BrNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-4-6-9(14)7-5-8/h4-7,10H,1-3H3,(H,15,18)(H,16,17)/t10-/m1/s1
• InChIKey: HFPMULXPVQWEJG-SNVBAGLBSA-N
• SMILES: CC(C)(C)OC(=O)N[C@H](C1=CC=C(C=C1)Br)C(=O)O

[(2R)-2-[(Tert-butoxy)carbonylamino]-2-(4-bromophenyl)acetic Acid（Cat No.:L018074）is a specialized chiral building block utilized in the synthesis of complex pharmaceutical compounds. The presence of a tert-butoxycarbonyl (Boc) group provides a protective functionality for the amino group, which is pivotal during peptide synthesis or other organic transformations requiring selective reactions. The 4-bromophenyl moiety enhances the molecule’s versatility, allowing for further functionalization through palladium-catalyzed coupling reactions. This compound is vital for researchers focusing on the development of new drugs, offering a reliable pathway for modifying bioactive molecules.