Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate

• CAT Number: L034235
• CAS Number: 69912-63-6
• Molecular Formula: C21H40N2O5
• Molecular Weight: 400.6
• Purity: ≥95%
• IUPAC Name: N-cyclohexylcyclohexanamine;(2S)-3-methoxy-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
• InChI: InChI=1S/C12H23N.C9H17NO5/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12;1-9(2,3)15-8(13)10-6(5-14-4)7(11)12/h11-13H,1-10H2;6H,5H2,1-4H3,(H,10,13)(H,11,12)/t;6-/m.0/s1
• InChIKey: IHZHDSHEYMELJP-ZCMDIHMWSA-N

Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate(CAT: L034235) is a chiral, protected amino acid ester that serves as a versatile intermediate in peptide synthesis and pharmaceutical research. This compound features a (S)-configured amino acid ester with a tert-butoxycarbonyl (Boc) protecting group on the amino functionality, which provides stability under various reaction conditions. The dicyclohexylamine counterion enhances solubility and facilitates purification in synthetic processes. Due to its chiral and protected structure, this compound is valuable in the synthesis of complex peptides, as well as in developing enantiomerically pure drug candidates. It is commonly used in pharmaceutical and biotechnological applications for creating bioactive molecules.