For research use only. Not for therapeutic Use.
Boc-D-norleucine(Cat No.:I043297)is a derivative of norleucine, where the D-enantiomer of the amino acid is protected by a tert-butoxycarbonyl (Boc) group at the N-terminal. The Boc group prevents unwanted reactions during peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The carboxyl group of norleucine remains free for coupling with other amino acids to form peptide chains. D-norleucine, a non-natural amino acid similar to leucine, is often incorporated into peptides to alter their hydrophobicity, structure, and bioactivity. This compound is valuable in peptide synthesis, drug discovery, and research applications.
CAS Number | 55674-63-0 |
Synonyms | (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid |
Molecular Formula | C11H21NO4 |
Purity | ≥95% |
IUPAC Name | (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid |
InChI | InChI=1S/C11H21NO4/c1-5-6-7-8(9(13)14)12-10(15)16-11(2,3)4/h8H,5-7H2,1-4H3,(H,12,15)(H,13,14)/t8-/m1/s1 |
InChIKey | ZIOCIQJXEKFHJO-MRVPVSSYSA-N |
SMILES | CCCC[C@H](C(=O)O)NC(=O)OC(C)(C)C |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |