(S)-Methyl 3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate

• CAT Number: L019822
• CAS Number: 266306-18-7
• Molecular Formula: C15H20BrNO4
• Molecular Weight: 358.23
• Purity: ≥95%
• IUPAC Name: methyl (2S)-3-(4-bromophenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoate
• InChI: InChI=1S/C15H20BrNO4/c1-15(2,3)21-14(19)17-12(13(18)20-4)9-10-5-7-11(16)8-6-10/h5-8,12H,9H2,1-4H3,(H,17,19)/t12-/m0/s1
• InChIKey: FDFQRJWLHKSHPZ-LBPRGKRZSA-N
• SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CC=C(C=C1)Br)C(=O)OC

(S)-Methyl 3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate（Cat No.:L019822）is a chiral, protected amino acid derivative featuring a methyl ester group, a para-bromophenyl side chain, and a Boc-protected amino group. With its (S)-configuration, this molecule is used as a building block in peptide synthesis and medicinal chemistry. The bromine atom on the aromatic ring allows for further functionalization via cross-coupling reactions, while the Boc group protects the amine during synthetic transformations. This compound is valuable for constructing complex molecules in drug development, asymmetric synthesis, and combinatorial chemistry, offering both reactivity and stereocontrol in various applications.