38254-63-6 Usage
Uses
Used in Pharmaceutical Industry:
S-(2-hydroxyethylmercapto)-L-cysteine is used as a therapeutic agent for its potential role in the treatment of certain medical conditions. Its unique structure allows it to interact with various biological targets, making it a promising candidate for drug development.
Used in Cosmetic Industry:
In the cosmetic industry, S-(2-hydroxyethylmercapto)-L-cysteine is used as an active ingredient for its antioxidant and skin-protective properties. It may help to reduce the signs of aging, protect the skin from environmental stressors, and maintain overall skin health.
Used in Research and Development:
S-(2-hydroxyethylmercapto)-L-cysteine is also utilized in research and development for its potential applications in various scientific fields. Its unique chemical properties make it an interesting subject for further study and exploration, with the potential to contribute to advancements in medicine, biotechnology, and other related areas.
Used in Environmental Applications:
S-(2-hydroxyethylmercapto)-L-cysteine may also find use in environmental applications, such as in the development of new materials for pollution control or water treatment. Its unique properties could be harnessed to create innovative solutions for environmental challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 38254-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38254-63:
(7*3)+(6*8)+(5*2)+(4*5)+(3*4)+(2*6)+(1*3)=126
126 % 10 = 6
So 38254-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO3S2/c6-4(5(8)9)3-11-10-2-1-7/h4,7H,1-3,6H2,(H,8,9)/t4-/m0/s1
38254-63-6Relevant academic research and scientific papers
Koide,Otaka,Fujii
, p. 1030 - 1034 (1993)
Disulfide bonds of peptides were effectively established between S- protected cysteine residues as well as free cysteine residues by the action of dimethylsulfoxide in trifluoroacetic acid. Oxytocin and α-human calcitonin gene-related peptide were synthesized using this oxidation system. The feasibility of this method for the formation of two disulfide bridges of apamin was also examined.
Keactions of cysteine sulfenyl thiocyanate with thiols to give unsymmetrical disulfides
Alguindigue Nimmo, Susan L.,Lemma, Kelemu,Ashby, Michael T.
, p. 467 - 471 (2008/02/08)
Cysteine sulfenyl thiocyanate (CSSCN) reacts with thiols at pH 0 to cleanly yield disulfides. 2-Mercaptoethanol (2-MESH), 3-mercaptopropionic acid (3-MPASH), penicillamine (PENSH), and glutathione (GSH) react with CSSCN to give the corresponding mixed disulfides: 2-MESSC, 3-MPASSC, PENSSC, and GSSC. These compounds are stable at pH 0 and have been characterized by 1H and 13C NMR spectroscopy.
