87402-76-4 Usage
Uses
Used in Pharmaceutical Applications:
3,4-bis(4-hydroxy-3-methoxybenzyl)tetrahydrofuran-2,3-diol is used as a potential therapeutic agent for its antioxidant properties, which may help in combating oxidative stress-related diseases. The presence of hydroxy and methoxy groups could also contribute to its antimicrobial capabilities, making it a candidate for treatments targeting various infections.
Used in Cosmetic Industry:
In the cosmetics field, 3,4-bis(4-hydroxy-3-methoxybenzyl)tetrahydrofuran-2,3-diol is utilized as an active ingredient for its potential to provide antioxidant benefits to the skin, protecting it from environmental stressors and promoting overall skin health. Its antimicrobial properties may also be leveraged to formulate products that support skin hygiene and prevent microbial imbalances.
Used in Scientific Research:
3,4-bis(4-hydroxy-3-methoxybenzyl)tetrahydrofuran-2,3-diol serves as a subject of interest in scientific research for its unique structural features and the possibility of exploring its biological activities further. Researchers may investigate its potential interactions with biological systems, mechanisms of action, and applications in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 87402-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,0 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87402-76:
(7*8)+(6*7)+(5*4)+(4*0)+(3*2)+(2*7)+(1*6)=144
144 % 10 = 4
So 87402-76-4 is a valid CAS Registry Number.
87402-76-4Relevant academic research and scientific papers
LIGNANS. 13. TOTAL SYNTHESES OF (-)-CARINOL, (-)-CARISSANOL AND (-)-HYDROXYTHUJAPLICA TIN METHYL ETHER
Khamlach, Kenza,Dhai, Robert,Brown, Eric
, p. 2195 - 2199 (2007/10/02)
The title compounds were obtained by α-hydroxylation of the corresponding optically active α,β-dibenzyl-γ-butyrolactones, followed by chemical reduction of the lactonic ring and/or catalytic hydrogenolysis of the O-benzyl protecting groups.
