126727-02-4 Usage
Description
Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]is a chemical compound derived from the amino acid valine, commonly used as a building block in the synthesis of various peptides and proteins. It is known for its ability to modify and stabilize the structure of peptides and proteins, making it a valuable tool in biochemical research, drug development, and the study of protein structures and functions.
Uses
Used in Biochemical Research:
Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]is used as a building block for the synthesis of peptides and proteins, enabling researchers to study protein structures and functions.
Used in Drug Development:
Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]is used as a modifying agent to stabilize the structure of peptides and proteins, potentially leading to the development of new therapeutic agents.
Used in Therapeutic Applications:
Valine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]possesses potential therapeutic properties and may be studied further for its pharmacological applications in various medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 126727-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,2 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126727-02:
(8*1)+(7*2)+(6*6)+(5*7)+(4*2)+(3*7)+(2*0)+(1*2)=124
124 % 10 = 4
So 126727-02-4 is a valid CAS Registry Number.
126727-02-4Relevant articles and documents
Determination of Chemical and Enantiomeric Purity of α-Amino Acids and their Methyl Esters as N-Fluorenylmethoxycarbonyl Derivatives Using Amylose-derived Chiral Stationary Phases
Islam, Md. Fokhrul,Adhikari, Suraj,Paik, Man-Jeong,Lee, Wonjae
, p. 332 - 338 (2019/04/13)
Liquid chromatographic enantiomer separation and simultaneous determination of chemical and enantiomeric purity of α-amino acids and their methyl esters as N-fluorenylmethoxycarbonyl (FMOC) derivatives was performed on three covalently bonded type chiral stationary phases (CSPs) derived from amylose derivatives. The enantiomer separation of α-amino acid esters as N-FMOC derivatives was better than that of the corresponding acids, especially for CSP 1 and 2. Chemical impurities as the corresponding racemic acids present in several commercially available racemic amino acid methyl esters were observed to be 0.49–17.50%. Enantiomeric impurities of several commercially available L-amino acid methyl esters were found to be 0.03–0.58%, whereas chemical impurities as the corresponding racemic acids present in the same analytes were found to be 0.13–13.62%. This developed analytical method will be useful for the determination of chemical and enantiomeric purity of α-amino acids and/or esters as N-FMOC derivatives using amylose-derived CSPs.