944283-25-4 Usage
Description
BOC-THR(FMOC-GLY)-OH is a chemical compound that consists of a protected form of threonine (BOC-THR) and a protected form of glycine (FMOC-GLY) linked by an ester bond. Threonine is an essential amino acid involved in protein synthesis and various metabolic processes, while glycine is a non-essential amino acid important for the production of proteins and enzymes. The BOC and FMOC groups act as protective groups to prevent unwanted reactions during chemical synthesis.
Uses
Used in Peptide Synthesis:
BOC-THR(FMOC-GLY)-OH is used as a building block for the synthesis of peptide chains. The protective groups BOC and FMOC ensure that the amino acids are stable and can be selectively deprotected and coupled during the synthesis process.
Used in Biochemical Research:
BOC-THR(FMOC-GLY)-OH is used as a research tool in biochemical studies. It can be employed to investigate the role of threonine and glycine in various biological processes, as well as to develop new methods for peptide synthesis and modification.
Check Digit Verification of cas no
The CAS Registry Mumber 944283-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,2,8 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 944283-25:
(8*9)+(7*4)+(6*4)+(5*2)+(4*8)+(3*3)+(2*2)+(1*5)=184
184 % 10 = 4
So 944283-25-4 is a valid CAS Registry Number.
944283-25-4Relevant articles and documents
"o-Acyl isopeptide method" for peptide synthesis: Synthesis of forty kinds of "o-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OH
Yoshiya, Taku,Taniguchi, Atsuhiko,Sohma, Youhei,Fukao, Fukue,Nakamura, Setsuko,Abe, Naoko,Ito, Nui,Skwarczynski, Mariusz,Kimura, Tooru,Hayashi, Yoshio,Kiso, Yoshiaki
, p. 1720 - 1730 (2008/02/10)
The O-acyl isopeptide method has recently received attention as an efficient synthetic method for peptides. Herein, forty kinds of "O-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OH (1-40) were effectively synthesized in two-steps without epimerization. The O-acyl isodipeptide units are important building blocks to enable the routine use of the O-acyl isopeptide method. This journal is The Royal Society of Chemistry.
