40661-45-8 Usage
Uses
Used in Pharmaceutical Industry:
4-[2-(β-D-Glucopyranosyloxy)ethyl]-4-hydroxy-2,5-cyclohexadien-1-one is used as a potential drug candidate for various health conditions due to its antioxidant and anti-inflammatory properties. Its ability to combat oxidative stress and reduce inflammation makes it a valuable asset in the development of new treatments for a range of diseases and disorders.
Used in Drug Delivery Systems:
In the pharmaceutical industry, 4-[2-(β-D-Glucopyranosyloxy)ethyl]-4-hydroxy-2,5-cyclohexadien-1-one can be utilized in drug delivery systems to enhance its bioavailability and therapeutic efficacy. By incorporating 4-[2-(β-D-Glucopyranosyloxy)ethyl]-4-hydroxy-2,5-cyclohexadien-1-one into various drug delivery platforms, such as nanoparticles or liposomes, its potential for targeted delivery and improved pharmacokinetics can be maximized, leading to more effective treatments.
Used in Nutraceutical Industry:
4-[2-(β-D-Glucopyranosyloxy)ethyl]-4-hydroxy-2,5-cyclohexadien-1-one can also be used in the nutraceutical industry as a dietary supplement or functional food ingredient. Its antioxidant and anti-inflammatory properties can provide health benefits when incorporated into products aimed at promoting overall wellness and reducing the risk of chronic diseases.
Used in Cosmetic Industry:
In the cosmetic industry, 4-[2-(β-D-Glucopyranosyloxy)ethyl]-4-hydroxy-2,5-cyclohexadien-1-one can be employed as an active ingredient in skincare products. Its antioxidant and anti-inflammatory properties can contribute to skin health by protecting against environmental stressors and reducing signs of aging, making it a valuable addition to anti-aging and skin-soothing formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 40661-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,6 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40661-45:
(7*4)+(6*0)+(5*6)+(4*6)+(3*1)+(2*4)+(1*5)=98
98 % 10 = 8
So 40661-45-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H20O8/c15-7-9-10(17)11(18)12(19)13(22-9)21-6-5-14(20)3-1-8(16)2-4-14/h1-4,9-13,15,17-20H,5-7H2/t9-,10-,11+,12-,13-/m0/s1
40661-45-8Relevant academic research and scientific papers
Synthesis of 13C-labeled possible intermediates in the biosynthesis of phenylethanoid derivatives, cornoside and rengyosides
Kuwajima, Hiroshi,Takai, Yoshitaka,Takaishi, Kiyokazu,Inoue, Kenichiro
, p. 581 - 586 (2007/10/03)
In order to clarify the biosynthetic pathway of C6-C2 unit compounds containing salidroside, cornoside, and rengyosides A and B in oleaceous plants, 13C-labeled putative precursors, 4-hydroxyphenylethanol, salidroside and cornoside, were prepared.
BIOGENESIS-LIKE TRANSFORMATION OF SALIDROSIDE TO RENGYOL AND ITS RELATED CYCLOHEXYLETANOIDS OF FORSYTHIA SUSPENSA
Endo, Katsuya,Seya, Kazuhiko,Hikino, Hiroshi
, p. 3673 - 3682 (2007/10/02)
Photooxygenation of salidroside (8) in methanol in presence of Rose Bengal afforded cornoside (9), which, on high pressure hydrogenation with 5percent palladium on activated carbon, yielded rengyoside B (6).Reduction of 6 with sodium borohydride gave rengyoside A(5) stereoselectively.By enzymatic hydrolysis, 9, 6 and 5 furnished rengyolone (4), rengyoxide (3) and rengyol (1), respectively. Similerly, p-hydroxyphenylethanol (10), the aglycone part of salidroside (8), was oxygenated photochemically to a dienone alcohol, which cyclized spontaneously to rengyolone (4).Hallerone (17) was obtained by the photooxygenation of p-hydroxyphenylethyl acetate (10b).Thus the plausible biosynthetic routes from salidroside (8) to rengyol (1) and the related natural cyclohexylethanoids were simulated chemically.
