2481-09-6 Usage
Description
S-tert-Butyl-L-cysteine hydrochloride is a protected form of L-Cysteine, a non-essential α-amino acid that is biosynthesized in humans. It plays a crucial role in various biological processes and has potential applications in different industries due to its unique properties.
Uses
Used in Pharmaceutical Industry:
S-tert-Butyl-L-cysteine hydrochloride is used as a precursor for the synthesis of various pharmaceutical compounds. Its role as a protected form of L-Cysteine allows for the development of drugs that can target specific biological pathways, making it a valuable component in drug discovery and design.
Used in Research and Development:
In the field of research and development, S-tert-Butyl-L-cysteine hydrochloride is used as a reagent for studying the properties and functions of L-Cysteine and its derivatives. This helps scientists understand the mechanisms of various biological processes and develop targeted therapies for various diseases.
Used in Nutraceutical Industry:
S-tert-Butyl-L-cysteine hydrochloride can be used as an additive in the nutraceutical industry, where it may contribute to the development of supplements and functional foods that promote health and well-being. Its role in the biosynthesis of L-Cysteine makes it a potential candidate for products aimed at supporting the immune system and overall health.
Used in Cosmetic Industry:
In the cosmetic industry, S-tert-Butyl-L-cysteine hydrochloride may be utilized for its antioxidant properties, which can help protect the skin from environmental stressors and promote a healthy, youthful appearance. It may also be used in the development of products that target specific skin concerns, such as aging or acne.
Used in Chemical Synthesis:
S-tert-Butyl-L-cysteine hydrochloride can be employed as a building block in the synthesis of various chemical compounds, including those with potential applications in materials science, electronics, and other industries. Its unique structure and properties make it a versatile component in the development of novel materials and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 2481-09-6 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 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2481-09:
(6*2)+(5*4)+(4*8)+(3*1)+(2*0)+(1*9)=76
76 % 10 = 6
So 2481-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO2S/c1-7(2,3)11-4-5(8)6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m0/s1
2481-09-6Relevant articles and documents
tert-Butyl group as thiol protection in peptide synthesis
Pastuszak, Juliusz Jacek,Chimiak, Andrzej
, p. 1868 - 1873 (2007/10/02)
S-tert-Butylcysteine was obtained by a new method. A number of its N-protected derivatives and esters were synthesized. Syntheses of several peptides containing tert-butyl and acetamidomethyl or benzyl thioethers of cysteine were carried out. The tert-butyl group was removed from the thiol group of peptides by treatment with (2-nitrophenyl)sulfenyl chloride (NpsCl). The S-(2-nitrophenyl)sulfenyl derivatives so obtained were converted either into cysteine by reduction or into cystine derivatives by disproportionation. Owing to the mild deprotection conditions and the great stability of the S-tert-butyl group, the other protecting groups, particularly those of the thiols, could be easily removed from a variety of combinations.