220497-51-8 Usage
Description
(S)-N-FMOC-(5-BROMO-2-METHOXYPHENYL)ALANINE is a chemical compound that features an alanine molecule, a nonessential amino acid vital for protein synthesis and energy production, bound to a 5-bromo-2-methoxyphenyl group and an FMOC (9-fluorenylmethyloxycarbonyl) protecting group. These additional groups are frequently utilized in organic synthesis and peptide chemistry for the modification and protection of functional groups within molecules. (S)-N-FMOC-(5-BROMO-2-METHOXYPHENYL)ALANINE is particularly valuable in research and pharmaceutical applications, serving as a building block for peptide synthesis and offering insights into the structure and function of proteins and peptides in biological systems.
Uses
Used in Pharmaceutical Applications:
(S)-N-FMOC-(5-BROMO-2-METHOXYPHENYL)ALANINE is used as a building block for peptide synthesis, contributing to the development of novel pharmaceutical compounds. Its unique structure aids in understanding the properties and functions of proteins and peptides, which can be crucial for designing effective drugs.
Used in Research and Development:
In the research industry, (S)-N-FMOC-(5-BROMO-2-METHOXYPHENYL)ALANINE is used as a key component in the study of protein and peptide structures. Its incorporation into various molecules allows scientists to investigate the effects of different functional groups on the overall behavior and interactions of these biomolecules.
Used in Organic Synthesis:
(S)-N-FMOC-(5-BROMO-2-METHOXYPHENYL)ALANINE is utilized as a modifying agent in organic synthesis, where the 5-bromo-2-methoxyphenyl group and the FMOC protecting group can be employed to protect and modify functional groups within target molecules, enhancing the efficiency and selectivity of chemical reactions.
Used in Peptide Chemistry:
In peptide chemistry, (S)-N-FMOC-(5-BROMO-2-METHOXYPHENYL)ALANINE is used as a protected amino acid for the synthesis of peptides. The FMOC protecting group ensures that the alanine molecule's functional groups remain intact during the synthesis process, allowing for the creation of complex peptide structures with specific properties and functions.
Check Digit Verification of cas no
The CAS Registry Mumber 220497-51-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,4,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 220497-51:
(8*2)+(7*2)+(6*0)+(5*4)+(4*9)+(3*7)+(2*5)+(1*1)=118
118 % 10 = 8
So 220497-51-8 is a valid CAS Registry Number.
