42390-97-6 Usage
Uses
Used in Pharmaceutical Research:
H-LYS(2-CL-Z)-OH is used as a research compound for exploring its potential effects and applications in the pharmaceutical industry. The attachment of the 2-chloro-Z group to lysine may provide new avenues for drug development, particularly in areas where lysine plays a significant role in biological processes.
Used in Biochemical Studies:
In the field of biochemistry, H-LYS(2-CL-Z)-OH is utilized as a modified amino acid to investigate its interactions with other biomolecules and its impact on protein structure and function. Understanding these interactions can lead to insights into the role of lysine in various biological systems and the potential for targeted therapies.
Used in Chemical Synthesis:
H-LYS(2-CL-Z)-OH serves as a building block in the synthesis of new compounds with specific properties. The 2-chloro-Z group may facilitate the creation of novel chemical entities with applications in various industries, including materials science, pharmaceuticals, and agrochemicals.
Used in Diagnostic Tools Development:
The unique properties of H-LYS(2-CL-Z)-OH may be harnessed in the development of diagnostic tools, such as biosensors or imaging agents, that rely on the specific interactions between lysine and other molecules. This could lead to more accurate and sensitive detection methods for various biological markers.
Check Digit Verification of cas no
The CAS Registry Mumber 42390-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,9 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42390-97:
(7*4)+(6*2)+(5*3)+(4*9)+(3*0)+(2*9)+(1*7)=116
116 % 10 = 6
So 42390-97-6 is a valid CAS Registry Number.
42390-97-6Relevant academic research and scientific papers
Facile synthesis of α-hydroxy carboxylic acids from the corresponding α-amino acids
Stuhr-Hansen, Nicolai,Padrah, Shahrokh,Str?mgaard, Kristian
supporting information, p. 4149 - 4151 (2015/02/02)
An effective and improved procedure is developed for the synthesis of α-hydroxy carboxylic acids by treatment of the corresponding protonated α-amino acid with tert-butyl nitrite in 1,4-dioxane-water. The amino moiety must be protonated and located α to a carboxylic acid function in order to undergo initial diazotization and successive hydroxylation, since neither β-amino acids nor acid derivatives such as esters and amides undergo hydroxylations. The method is successfully applied for the synthesis of 18 proteinogenic amino acids.
New Side-Chain Protecting Groups for Lysine and Tyrosine Suitable for Solid-Phase Peptide Synthesis
Salem, Ezzeldin M.,Schou, O.
, p. 62 - 64 (2007/10/02)
The syntheses of two new lysine and tyrosine derivatives, Boc-Lys(2-ClZ) and Boc-Tyr(2-BrBzl) have been described.Their use in the solid-phase peptide synthesis of the decapeptide Glu-Arg(NO2)-Gly-Phe-Phe-Tyr-Thr-Pro-Lys-Thr (I) corresponding to the seque
