219967-68-7 Usage
Uses
Used in Pharmaceutical Industry:
FMoc-β-Lys(Boc)-OH serves as a crucial building block for the synthesis of bioactive peptides and proteins, which are vital for the development of new drugs and therapeutic agents. Its role in the stepwise assembly of peptide chains through solid-phase peptide synthesis allows for the precise construction of complex peptide structures with specific biological functions.
Used in Research and Development:
In the field of research, FMoc-β-Lys(Boc)-OH is utilized as a key component in the synthesis of custom peptides for various experimental purposes. This includes the study of peptide-protein interactions, the development of peptide-based vaccines, and the exploration of novel peptide-based therapeutics.
Used in Diagnostics:
FMoc-β-Lys(Boc)-OH contributes to the creation of diagnostic agents, such as peptide-based probes and markers, which are employed in the detection and monitoring of diseases at the molecular level.
Used in Biochemistry Education:
As an essential component in peptide synthesis, FMoc-β-Lys(Boc)-OH is also used in educational settings to teach students the principles of organic chemistry, protein synthesis, and the techniques involved in peptide chemistry.
Overall, FMoc-β-Lys(Boc)-OH is a versatile compound with applications spanning across various sectors, including pharmaceuticals, research, diagnostics, and education, due to its role in the synthesis of peptides and proteins with diverse biological activities and potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 219967-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,9,6 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 219967-68:
(8*2)+(7*1)+(6*9)+(5*9)+(4*6)+(3*7)+(2*6)+(1*8)=187
187 % 10 = 7
So 219967-68-7 is a valid CAS Registry Number.
219967-68-7Relevant academic research and scientific papers
Abele, Stefan,Guichard, Gilles,Seebach, Dieter
, p. 2141 - 2156 (1998)
For further structural studies and for physiological investigations of β-peptides, it is necessary to have H2O-soluble derivatives. Thus, we have prepared β-hexa-, β-hepta-, and β-nonapeptides (1-6) with two, three, and seven side chains of lys
