For research use only. Not for therapeutic Use.
Boc-N-methyl-L-isoleucine(Cat No.:I043249)is a derivative of L-isoleucine where the N-terminal amine group is protected by a tert-butoxycarbonyl (Boc) group, and the amino group of isoleucine is methylated to form N-methyl-L-isoleucine. This modification prevents unwanted side reactions during peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). The Boc group allows selective deprotection during peptide elongation, while the N-methyl group introduces steric and electronic changes that can impact peptide conformation, stability, and hydrophobicity. This compound is used to synthesize modified peptides for research in drug development and bioactive peptide studies.
CAS Number | 52498-32-5 |
Synonyms | (2S,3S)-3-methyl-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]pentanoic acid |
Molecular Formula | C12H23NO4 |
Purity | ≥95% |
IUPAC Name | (2S,3S)-3-methyl-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]pentanoic acid |
InChI | InChI=1S/C12H23NO4/c1-7-8(2)9(10(14)15)13(6)11(16)17-12(3,4)5/h8-9H,7H2,1-6H3,(H,14,15)/t8-,9-/m0/s1 |
InChIKey | HTBIAUMDQYXOFG-IUCAKERBSA-N |
SMILES | CC[C@H](C)[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |