218457-81-9 Usage
Uses
Used in Scientific Research:
FMOC-D-3,4-DIMETHOXYPHENYLALANINE is used as a research compound for its role in solid-phase peptide synthesis (SPPS) techniques. It aids in the construction of peptide chains, which is crucial for various biological and pharmaceutical studies.
Used in Pharmaceutical Industry:
FMOC-D-3,4-DIMETHOXYPHENYLALANINE is used as a building block in the synthesis of peptides and proteins, which are vital for the development of new drugs and therapeutic agents. Its application in this industry is focused on facilitating the creation of complex molecular structures that can be used for medicinal purposes.
Used in Laboratory Research:
FMOC-D-3,4-DIMETHOXYPHENYLALANINE is used as a reagent in laboratory settings for conducting experiments and studies related to peptide chemistry. Its presence in solid-phase peptide synthesis techniques makes it an essential component for researchers working on peptide-based projects.
Check Digit Verification of cas no
The CAS Registry Mumber 218457-81-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,4,5 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 218457-81:
(8*2)+(7*1)+(6*8)+(5*4)+(4*5)+(3*7)+(2*8)+(1*1)=149
149 % 10 = 9
So 218457-81-9 is a valid CAS Registry Number.
218457-81-9Relevant academic research and scientific papers
New synthetic amino acids for the design and synthesis of peptide-based metal ion sensors
Torrado, Alicia,Imperiali, Barbara
, p. 8940 - 8948 (2007/10/03)
The syntheses of two new nonstandard amino acids, Flu (6) and XBp (20), and a new synthesis of Dmd (12) are reported. These residues exhibit fluorescence, metal-coordination, and fluorescence-quenching properties, respectively. These building blocks have been incorporated into peptides via solid phase peptide synthesis to afford the prototype for a photoinduced electron transfer-based metal ion chemosensor. The fluorescence of the peptides is modulated upon metal binding. This results from a metal ion-induced conformational change that brings the side chains of the Flu and Dmd amino acids into proximity, thereby favoring photoinduced electron transfer (PET) fluorescence quenching.
