6154-39-8 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
Z-GLY-GLN-OH is used as a building block in the synthesis of longer peptides and proteins, facilitating the development of new pharmaceutical agents and therapeutics. Its presence in the synthesis process helps in creating complex peptide structures with specific biological activities.
Used in Biochemical Studies and Peptide Chemistry:
Z-GLY-GLN-OH serves as a model compound in biochemical studies, allowing researchers to investigate the synthesis and properties of peptides. It provides insights into the behavior of dipeptides and their interactions with other molecules, contributing to a better understanding of peptide chemistry.
Used in Peptide Synthesis:
Z-GLY-GLN-OH is used as a protected dipeptide in the synthesis of larger peptide chains. The Z-protection group on the amino terminus of the glycine residue prevents unwanted side reactions during the synthesis process, ensuring the formation of the desired peptide sequence.
Check Digit Verification of cas no
The CAS Registry Mumber 6154-39-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6154-39:
(6*6)+(5*1)+(4*5)+(3*4)+(2*3)+(1*9)=88
88 % 10 = 8
So 6154-39-8 is a valid CAS Registry Number.
6154-39-8Relevant academic research and scientific papers
Peptide coupling of unprotected amino acids through in situ p-nitrophenyl ester formation
Gagnon, Paul,Huang, Xicai,Therrien, Eric,Keillor, Jeffrey W.
, p. 7717 - 7719 (2007/10/03)
Several series of dipeptides and tripeptides were prepared via an activation-coupling method involving the in situ formation of a p-nitrophenyl ester of an (N-protected) amino acid, followed by coupling with an unprotected amino acid in partially aqueous solutions. The resulting peptide is easily isolated by precipitation. In general, the yields obtained are good to excellent and racemization is minimal. This method is particularly advantageous with respect to its simplicity and lack of obligatory side chain protection/deprotection steps.
