(S)-tert-Butyl (1-(3-bromophenyl)-2-hydroxyethyl)carbamate

• CAT Number: L018392
• CAS Number: 910308-92-8
• Molecular Formula: C13H18BrNO3
• Molecular Weight: 316.19
• Purity: ≥95%
• IUPAC Name: tert-butyl N-[(1S)-1-(3-bromophenyl)-2-hydroxyethyl]carbamate
• InChI: InChI=1S/C13H18BrNO3/c1-13(2,3)18-12(17)15-11(8-16)9-5-4-6-10(14)7-9/h4-7,11,16H,8H2,1-3H3,(H,15,17)/t11-/m1/s1
• InChIKey: CYSVECFBQRKMKO-LLVKDONJSA-N
• SMILES: CC(C)(C)OC(=O)N[C@H](CO)C1=CC(=CC=C1)Br

(S)-tert-Butyl (1-(3-bromophenyl)-2-hydroxyethyl)carbamate（Cat No.:L018392）is a chiral carbamate compound featuring a (3-bromophenyl)ethyl backbone with a hydroxyl group at the 2-position and a Boc (tert-butoxycarbonyl) protecting group on the amine. The (S)-configuration provides stereochemical definition, making it valuable in asymmetric synthesis and pharmaceutical development. The Boc group protects the nitrogen during multi-step reactions and can be easily removed under acidic conditions. The hydroxyl functionality allows for further derivatization, such as esterification or etherification. This compound serves as a key intermediate in the synthesis of enantiomerically pure bioactive molecules and medicinal chemistry scaffolds.