Cbz-Aib-Leu-OMe
Need Assistance?
  • US & Canada:
    +
  • UK: +

Cbz-Aib-Leu-OMe

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Cbz-Aib-Leu-OMe is a protected dipeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the α-aminoisobutyric acid (Aib) residue, preventing unwanted reactions during synthesis. Aib is a non-natural amino acid that induces helical structures in peptides due to its steric properties. Leu (Leucine) is the second amino acid in the sequence, known for its hydrophobic character, contributing to the overall structure and stability of the peptide. The OMe (methyl ester) group at the C-terminus indicates that the carboxyl group is esterified, which can be useful in strategies where further peptide extension or specific cleavage is required. This compound is employed to introduce both structural constraints and hydrophobic properties into peptides, enhancing their desired functional characteristics.

Category
Peptide Synthesis Reagents
Catalog number
BAT-016537
CAS number
866919-63-3
Molecular Formula
C19H28N2O5
Molecular Weight
364.44
Cbz-Aib-Leu-OMe
Synonyms
N-Benzoxycarbonyl-alpha-methyl-alanyl-L-leucine methyl ester; Methyl (2-(((benzyloxy)carbonyl)amino)-2-methylpropanoyl)-L-leucinate; Z-Aib-Leu-OMe; L-Leucine, 2-methyl-N-[(phenylmethoxy)carbonyl]alanyl-, methyl ester; 2-Methyl-N-[(phenylmethoxy)carbonyl]alanyl-L-leucine methyl ester
Purity
≥95%
Density
1.116±0.06 g/cm3
Melting Point
78-80 °C
Boiling Point
525.8±40.0 °C at 760 mmHg
Sequence
Cbz-Aib-Leu-OMe
InChI
InChI=1S/C19H28N2O5/c1-13(2)11-15(16(22)25-5)20-17(23)19(3,4)21-18(24)26-12-14-9-7-6-8-10-14/h6-10,13,15H,11-12H2,1-5H3,(H,20,23)(H,21,24)/t15-/m0/s1
InChI Key
LBJMILKEAJFUDH-HNNXBMFYSA-N
Canonical SMILES
COC(C(CC(C)C)NC(C(NC(OCC1=CC=CC=C1)=O)(C)C)=O)=O
Online Inquiry
Verification code
Inquiry Basket