(2S,3S,5S)-2-Amino-3-hydroxy-5-(tert-butyloxycarbonylamino)-1,6-diphenylhexane

• CAT Number: R006256
• CAS Number: 144163-85-9
• Molecular Formula: C23H32N2O3
• Molecular Weight: 384.52
• Purity: ≥95%
• Synonyms: N-[(1S,3S,4S)-4-Amino-3-hydroxy-5-phenyl-1-(phenylmethyl)pentyl]carbamic Acid 1,1-Dimethylethyl Ester; N-[(1S,3S,4S)-1-Benzyl-3-hydroxy-5-phenyl-4-aminopentyl]carbamic Acid tert-Butyl Ester
• Storage: Desiccate at +4C
• IUPAC Name: tert-butyl N-[(2S,4S,5S)-5-amino-4-hydroxy-1,6-diphenylhexan-2-yl]carbamate
• InChI: InChI=1S/C23H32N2O3/c1-23(2,3)28-22(27)25-19(14-17-10-6-4-7-11-17)16-21(26)20(24)15-18-12-8-5-9-13-18/h4-13,19-21,26H,14-16,24H2,1-3H3,(H,25,27)/t19-,20-,21-/m0/s1
• InChIKey: UKFHOTNATOJBKZ-ACRUOGEOSA-N
• SMILES: CC(C)(C)OC(=O)NC(CC1=CC=CC=C1)CC(C(CC2=CC=CC=C2)N)O

(2S,3S,5S)-2-Amino-3-hydroxy-5-(tert-butyloxycarbonylamino)-1,6-diphenylhexane (Cat No.: R006256) is a chiral, multifunctional compound used as an intermediate in the synthesis of peptide-based drugs and biologically active molecules. Its three stereocenters confer defined spatial orientation, essential for receptor binding and biological activity. The tert-butyloxycarbonyl (Boc) group protects the amino functionality during chemical transformations, while the hydroxyl and diphenyl groups enable further derivatization. This compound is particularly valuable in medicinal chemistry for developing protease inhibitors and other therapeutics requiring stereochemically controlled side chains.