125814-22-4 Usage
Uses
Used in Pharmaceutical Development:
NOMEGA-tert-Butoxycarbonyl-NALPHA-9-fluorenylmethoxycarbonyl-L-lysine NALPH is used as a building block in the synthesis of peptides for various pharmaceutical applications. Its unique structure allows for the controlled assembly of peptide sequences, which is crucial for the development of new drugs with specific therapeutic properties.
Used in Peptide Research and Development:
In the field of peptide chemistry, NOMEGA-tert-Butoxycarbonyl-NALPHA-9-fluorenylmethoxycarbonyl-L-lysine NALPH serves as a key component in research and development activities. It enables scientists to explore the properties and potential applications of novel peptide sequences, contributing to the advancement of peptide-based therapies and diagnostic tools.
Used in Peptide Synthesis Methodologies:
NOMEGA-tert-Butoxycarbonyl-NALPHA-9-fluorenylmethoxycarbonyl-L-lysine NALPH is utilized as a protected amino acid in solid-phase peptide synthesis (SPPS) and liquid-phase peptide synthesis (LPPS) methodologies. The presence of the Boc and Fmoc protecting groups allows for the stepwise addition of amino acids to a growing peptide chain, ensuring the correct sequence and minimizing side reactions.
Used in Biochemical and Analytical Applications:
NOMEGA-tert-Butoxycarbonyl-NALPHA-9-fluorenylmethoxycarbonyl-L-lysine NALPH is also employed in various biochemical and analytical applications, such as the synthesis of bioactive peptides for use in assays, the development of peptide-based sensors, and the study of protein-protein interactions. Its controlled synthesis capabilities make it a valuable tool in these research areas.
Used in Cosmetics and Personal Care Industry:
NOMEGA-tert-Butoxycarbonyl-NALPHA-9-fluorenylmethoxycarbonyl-L-lysine NALPH can be used in the development of cosmetic and personal care products, where peptide-based ingredients are increasingly sought after for their potential benefits in skin care, hair care, and other applications. NOMEGA-tert-Butoxycarbonyl-NALPHA-9-fluorenylmethoxycarbonyl-L-lysine NALPH's role in peptide synthesis allows for the creation of targeted and effective ingredients for these products.
Check Digit Verification of cas no
The CAS Registry Mumber 125814-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,8,1 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125814-22:
(8*1)+(7*2)+(6*5)+(5*8)+(4*1)+(3*4)+(2*2)+(1*2)=114
114 % 10 = 4
So 125814-22-4 is a valid CAS Registry Number.
