CAS 116747-54-7
:Fmoc-Ala-Gly-OH
Fmoc-Ala-Gly-OH
CAS:Bachem ID: 4012679.
Formel:C20H20N2O5Reinheit:99.3%Farbe und Form:White PowderMolekulargewicht:368.39Glycine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanyl-
CAS:Formel:C20H20N2O5Reinheit:98%Farbe und Form:SolidMolekulargewicht:368.3832N-[N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-alanyl]-glycine
CAS:Kontrolliertes ProduktApplications FMOC-ALA-GLY-OH (cas# 116747-54-7) is a useful research chemical.
Formel:C20H20N2O5Farbe und Form:NeatMolekulargewicht:368.383Fmoc-Ala-Gly-OH
CAS:Fmoc-Ala-Gly-OH is a cell-surface residue that is found on proteins. It is the ligand for a number of protein receptors and has been shown to be involved in factors such as orientation, verotoxin, and neoglycopeptides. Fmoc-Ala-Gly-OH also acts as an inhibitor by binding to glycine and trisaccharide residues. This residue is located at the N-terminal of the protein.Formel:C20H20N2O5Reinheit:Min. 95%Molekulargewicht:368.38 g/molFmoc-Ala-Gly-OH
CAS:Fmoc-Ala-Gly-OH is a building block for peptide synthesis and Fmoc protected l-amino acid. It is an amino acid that belongs to the group of Fmoc protected l-amino acids. This amino acid can be used as a building block for peptide synthesis, which is a technique for the chemical synthesis of peptides. The general method involves the activation of carboxyl groups on one end of the growing peptide chain with an activating agent such as dicyclohexylcarbodiimide or diisopropylcarbodiimide. The activated carboxyl group reacts with an amine (or ammonia) to form an amide bond, linking the new molecule to the preceding one in the chain. This reaction produces a molecule with a free carboxyl group at one end, which can then repeat the process.
Formel:C20H20N2O5Reinheit:Min. 95%Molekulargewicht:368.39 g/mol





