566172-19-8 Usage
Description
N-tert-Butyloxycarbonyl Glutathione DiMethyl Diester Disulfide DiMer is a chemical compound derived from glutathione, a naturally occurring peptide found in cells that plays a critical role in various biological processes, including detoxification and immune system regulation. N-tert-Butyloxycarbonyl Glutathione DiMethyl Diester Disulfide DiMer is characterized by its unique structure, which includes a tert-butyloxycarbonyl group, two methyl ester groups, and a disulfide bond, making it a valuable intermediate in the synthesis of glutathione and its derivatives.
Uses
Used in Pharmaceutical Industry:
N-tert-Butyloxycarbonyl Glutathione DiMethyl Diester Disulfide DiMer is used as an intermediate in the synthesis of Glutathione (G597951) and its derivatives for various pharmaceutical applications. Glutathione is known for its antioxidant, detoxifying, and immune-boosting properties, making it a crucial component in the development of drugs targeting a wide range of health conditions, including oxidative stress, inflammation, and immune disorders.
Used in Cosmetic Industry:
In the cosmetic industry, N-tert-Butyloxycarbonyl Glutathione DiMethyl Diester Disulfide DiMer may be utilized as a precursor for the development of glutathione-based skincare products. Glutathione is known for its skin-lightening and anti-aging properties, making it a popular ingredient in various cosmetic formulations aimed at improving skin health and appearance.
Used in Research and Development:
N-tert-Butyloxycarbonyl Glutathione DiMethyl Diester Disulfide DiMer can also be employed in research and development settings, where it may be used to study the properties and functions of glutathione and its role in cellular processes. By understanding the structure and activity of N-tert-Butyloxycarbonyl Glutathione DiMethyl Diester Disulfide DiMer, researchers can gain valuable insights into the development of new therapeutic strategies and drug candidates targeting glutathione-related pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 566172-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,6,1,7 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 566172-19:
(8*5)+(7*6)+(6*6)+(5*1)+(4*7)+(3*2)+(2*1)+(1*9)=168
168 % 10 = 8
So 566172-19-8 is a valid CAS Registry Number.
566172-19-8Relevant articles and documents
A convenient catalyst for aqueous and protein Suzuki-Miyaura cross-coupling
Chalker, Justin M.,Wood, Charlotte S. C.,Davis, Benjamin G.
supporting information; experimental part, p. 16346 - 16347 (2010/01/29)
(Figure Presented) A phosphine-free palladium catalyst for aqueous Suzuki-Miyaura cross-coupling is presented. The catalyst is active enough to mediate hindered, ortho-substituted biaryl couplings but mild enough for use on peptides and proteins. The Suzuki-Miyaura couplings on protein substrates are the first to proceed in useful conversions. Notably, hydrophobic aryl and vinyl groups can be transferred to the protein surface without the aid of organic solvent since the aryl- and vinylboronic acids used in the coupling are water-soluble as borate salts. The convenience and activity of this catalyst prompts use in both general synthesis and bioconjugation.
