2488-24-6 Usage
Uses
Used in Pharmaceutical Industry:
Z-THR-SER-OME is used as a therapeutic agent for its potential role in modulating immune responses and protein synthesis, given the presence of threonine, which is essential for these functions.
Used in Biochemical Research:
Z-THR-SER-OME serves as a research tool for studying the biosynthesis of purines and pyrimidines, as well as the role of serine as a precursor for other amino acids, contributing to a deeper understanding of metabolic pathways.
Used in Nutritional Supplements:
As a dietary supplement, Z-THR-SER-OME may be used to support protein synthesis and overall amino acid balance in the body, potentially benefiting individuals with specific nutritional needs.
Used in Cosmetics and Personal Care:
Z-THR-SER-OME could be utilized in cosmetic formulations for its potential role in skin health and regeneration, leveraging the properties of the constituent amino acids, particularly threonine and serine, which are known to be beneficial for skin integrity.
Used in Agricultural Applications:
In agriculture, Z-THR-SER-OME might be employed to enhance plant growth and health, given the role of amino acids in plant nutrition and development, especially in the context of ornithine's involvement in nitrogen metabolism.
Check Digit Verification of cas no
The CAS Registry Mumber 2488-24-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,8 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2488-24:
(6*2)+(5*4)+(4*8)+(3*8)+(2*2)+(1*4)=96
96 % 10 = 6
So 2488-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H22N2O7/c1-10(20)13(14(21)17-12(8-19)15(22)24-2)18-16(23)25-9-11-6-4-3-5-7-11/h3-7,10,12-13,19-20H,8-9H2,1-2H3,(H,17,21)(H,18,23)
2488-24-6Relevant academic research and scientific papers
Chlorosulfite, a Versatile and Mild Condensation Reagent for the Synthesis of Peptides
Appel, Rolf,Glaesel, Ursula,Glaesel, Volker Ingo
, p. 1542 - 1545 (2007/10/02)
The title compound 5, which can be easily obtained from hexamethylphosphoric triamide (1) and thionyl chloride by catalysis of dimethylformamide, is succesfully applied as a mild condensation reagent for the synthesis of peptides.
Method for removal of thiol-protecting groups
-
, (2008/06/13)
A novel method for removal of protective group(s) from an amino acid or peptide having thiol group(s) protected with p-methoxybenzyl, 1-adamantyl or t-butyl group by treating the protected amino acid or peptide with the mercuric salt of acetic acid or halogenoacetic acid, the removal being effected selectively and very smoothly in a good yield under extremely mild conditions without giving any undesirable influence upon other functional or protective group(s).
