Dicyclohexylamine (R)-2-((tert-butoxycarbonyl)amino)-5-phenylpentanoate

• CAT Number: L026818
• CAS Number: 919529-74-1
• Molecular Formula: C28H46N2O4
• Molecular Weight: 474.70
• Purity: ≥95%
• IUPAC Name: N-cyclohexylcyclohexanamine;(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-phenylpentanoic acid
• InChI: InChI=1S/C16H23NO4.C12H23N/c1-16(2,3)21-15(20)17-13(14(18)19)11-7-10-12-8-5-4-6-9-12;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-6,8-9,13H,7,10-11H2,1-3H3,(H,17,20)(H,18,19);11-13H,1-10H2/t13-;/m1./s1
• InChIKey: WTRAZOVTEAIRDM-BTQNPOSSSA-N
• SMILES: CC(C)(C)OC(=O)NC(CCCC1=CC=CC=C1)C(=O)O.C1CCC(CC1)NC2CCCCC2

Dicyclohexylamine (R)-2-((tert-butoxycarbonyl)amino)-5-phenylpentanoate（Cat No.:L026818）is a chiral intermediate used in the synthesis of peptides and other complex organic molecules, particularly in pharmaceutical research. This compound features a (R)-2-amino-5-phenylpentanoate backbone protected by a tert-butoxycarbonyl (Boc) group, with dicyclohexylamine as a counterion. It is crucial in the development of enantiomerically pure drugs, where stereoselectivity is essential for biological activity. Its role in peptide synthesis and drug discovery makes it a valuable tool in the production of therapeutic agents and advanced organic compounds.