214852-35-4 Usage
Description
FMOC-D-ASP-OFM, also known as N-(9-fluorenylmethoxycarbonyl)-D-aspartic acid alpha-methyl ester, is a chemical compound that serves as a crucial component in peptide synthesis and solid-phase peptide synthesis. It is a derivative of aspartic acid, a naturally occurring amino acid in proteins, which has been modified with an alpha-methyl ester group to enhance its stability and reactivity. The FMOC group in FMOC-D-ASP-OFM acts as a protective agent for the carboxyl group of aspartic acid, facilitating stepwise peptide synthesis while preventing unwanted side reactions. FMOC-D-ASP-OFM is widely utilized in the creation of peptide-based drugs and in the research and development of novel peptide-based materials and technologies, making it a versatile tool in peptide chemistry for the controlled and efficient synthesis of complex peptides with specific sequences and properties.
Uses
Used in Pharmaceutical Industry:
FMOC-D-ASP-OFM is used as a key building block for the synthesis of peptide-based drugs, contributing to the development of new therapeutic agents with specific biological activities. Its role in peptide synthesis allows for the creation of drugs with targeted effects and improved pharmacokinetic properties.
Used in Research and Development:
FMOC-D-ASP-OFM is utilized as a research tool for the exploration and development of new peptide-based materials and technologies. Its application in this field aids scientists in understanding the structure-function relationships of peptides and in designing innovative therapeutics and diagnostic tools.
Used in Peptide Synthesis:
FMOC-D-ASP-OFM is used as a protected amino acid in the synthesis of complex peptides, ensuring the controlled addition of amino acid residues and preventing side reactions that could compromise the integrity and function of the final peptide product.
Used in Solid-Phase Peptide Synthesis (SPPS):
FMOC-D-ASP-OFM is employed as a protected amino acid in solid-phase peptide synthesis, a technique that allows for the stepwise assembly of peptides on an insoluble resin support. This method enhances the efficiency and purity of peptide synthesis, making it a preferred approach for the production of large quantities of peptide-based compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 214852-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,8,5 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 214852-35:
(8*2)+(7*1)+(6*4)+(5*8)+(4*5)+(3*2)+(2*3)+(1*5)=124
124 % 10 = 4
So 214852-35-4 is a valid CAS Registry Number.
