25552-06-1 Usage
Uses
Used in Pharmaceutical Applications:
(2R,6S)-(+)-4-Benzyloxy-2-benzoyloxymethyl-6-methoxy-2H-pyran-3(6H)-one is used as a pharmaceutical agent for its antimicrobial properties, making it a candidate for the development of new drugs targeting various infections.
Used in Skincare Products:
In the skincare industry, (2R,6S)-(+)-4-Benzyloxy-2-benzoyloxymethyl-6-methoxy-2H-pyran-3(6H)-one is used as an antioxidant ingredient to protect the skin from oxidative stress and promote overall skin health.
Used in Adhesives and Coatings:
(2R,6S)-(+)-4-Benzyloxy-2-benzoyloxymethyl-6-methoxy-2H-pyran-3(6H)-one is used as an additive in adhesives and coatings to improve adhesion and enhance resistance to oxidation, thereby increasing the durability and performance of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 25552-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25552-06:
(7*2)+(6*5)+(5*5)+(4*5)+(3*2)+(2*0)+(1*6)=101
101 % 10 = 1
So 25552-06-1 is a valid CAS Registry Number.
25552-06-1Relevant academic research and scientific papers
3- and 4-uloses derived from N-acetyl- D -glucosamine: A unique pair of complementary organocatalysts for asymmetric epoxidation of alkenes
Schoeberl, Christof,Jaeger, Volker
supporting information; experimental part, p. 790 - 796 (2012/05/04)
The 4-ulose and the 3-ulose, both derived in two steps from the α-methyl glycoside of N-acetyl-D-glucosamine (GlcNAc), act as organocatalysts in the asymmetric epoxidation of alkenes, with unprecedented complementary enantioselectivity. The best results are found with α,β-unsaturated esters as substrates, with enantiomeric ratios up to 90:10 and 11:89, respectively. Copyright
