19720-12-8 Usage
Uses
Used in Biochemistry Research:
Z-ASP-OME DCHA is used as a reagent for the synthesis of peptides amidating enzymes and in protease studies. Its application in these areas is crucial for understanding the structure and function of proteins, as well as their interactions within biological systems.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Z-ASP-OME DCHA is used as a building block for the development of new drugs. Its role in peptide synthesis allows researchers to create novel compounds with potential therapeutic applications.
Used in Academic Research:
Z-ASP-OME DCHA is utilized in academic institutions for teaching and research purposes. It serves as a valuable tool for students and researchers to learn about peptide synthesis, enzymatic reactions, and other biochemical processes.
Used in Diagnostic Applications:
In the field of diagnostics, Z-ASP-OME DCHA may be employed in the development of assays and tests that rely on the detection or manipulation of specific proteins or enzymes. Its use in these applications can contribute to the advancement of diagnostic techniques and the identification of biomarkers for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 19720-12-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,2 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19720-12:
(7*1)+(6*9)+(5*7)+(4*2)+(3*0)+(2*1)+(1*2)=108
108 % 10 = 8
So 19720-12-8 is a valid CAS Registry Number.
19720-12-8Relevant academic research and scientific papers
Tetrazole analogues of aspartic, glutamic and α-aminoadipic acids and their derivatives with tetrazole ring in side chains useful for solid-phase peptide synthesis
Manturewicz,Grzonka
, p. 2121 - 2131 (2008/09/18)
Tetrazole analogues of Fmoc-aspartic, -glutamic and -α-aminoadipic acids with acidic tetrazolyl group in side chains suitable for solid-phase peptide synthesis were obtained. Moreover, the appropriate derivatives of aspartic and glutamic acids containing tetrazole ring methylated in position N1 or N2 were synthesized as well.
