148616-91-5 Usage
General Description
OCTYL THIOMALTOSIDE is a non-ionic detergent and a mild solubilizing agent that is often used in protein research and biochemistry. It is derived from maltose and contains an octyl hydrophobic tail, making it effective at solubilizing and stabilizing membrane proteins. OCTYL THIOMALTOSIDE is commonly utilized in the extraction and purification of membrane proteins, as well as in the study of protein-protein interactions and structural biology. Additionally, it is known for its low toxicity and biocompatibility, making it a popular choice for use in biological and biomedical applications. Overall, OCTYL THIOMALTOSIDE is a versatile and valuable chemical for the study and manipulation of proteins and membranes in research and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 148616-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,6,1 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 148616-91:
(8*1)+(7*4)+(6*8)+(5*6)+(4*1)+(3*6)+(2*9)+(1*1)=155
155 % 10 = 5
So 148616-91-5 is a valid CAS Registry Number.
148616-91-5Relevant articles and documents
Preparation of S-glycoside surfactants and cysteine thioglycosides using minimally competent Lewis acid catalysis
Szabó, Lajos Z.,Hanrahan, Dillon J.,Jones, Evan M.,Martin, Erin,Pemberton, Jeanne E.,Polt, Robin
, p. 1 - 4 (2016)
Here we report a method for the preparation of anomerically pure β-S-glycopyranosides (1,2-trans-glycosides) from the corresponding peracetate donors. S-glycosylation was performed in CHCl3 at reflux in the presence of a catalytic amount of InBr3. Deacylation of the intermediate peracetates were achieved under Zemplén conditions. Five pyranose examples, monosaccharides D-glucose and D-galactose and disaccharides cellobiose, maltose, and lactose, were used as donors, and five thiols including an α/ω dithiol and Fmoc-L-cysteine were used as acceptors. Melting points, high res MS, [α]D and NMR data (1H and 13C, including COSY, HSQC and HMBC) are reported for compounds not previously described.
