492450-55-2 Usage
Uses
Used in Pharmaceutical Industry:
2,3,4,5,6,7,8,10A-OCTAHYDRO-XANTHEN-1-ONE is used as a synthetic intermediate for the preparation of various drugs and pharmaceuticals. Its versatile nature allows it to be a key component in the development of new medications.
Used in Fragrance Industry:
2,3,4,5,6,7,8,10A-OCTAHYDRO-XANTHEN-1-ONE is used as a fragrance ingredient for its pleasant, floral aroma, contributing to the creation of various scent profiles in perfumes and other fragranced products.
Used in Antimicrobial Applications:
2,3,4,5,6,7,8,10A-OCTAHYDRO-XANTHEN-1-ONE is used as an antimicrobial agent due to its potential to inhibit the growth of certain microorganisms, making it a valuable component in sanitizing and preserving products.
Used in Antioxidant Applications:
2,3,4,5,6,7,8,10A-OCTAHYDRO-XANTHEN-1-ONE is used as an antioxidant, helping to prevent oxidative damage in various products, including pharmaceuticals and cosmetics, by neutralizing free radicals.
Used in Anticancer Applications:
2,3,4,5,6,7,8,10A-OCTAHYDRO-XANTHEN-1-ONE is used in research for its potential anticancer properties, with the aim of developing new therapeutic agents for the treatment of various types of cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 492450-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,2,4,5 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 492450-55:
(8*4)+(7*9)+(6*2)+(5*4)+(4*5)+(3*0)+(2*5)+(1*5)=162
162 % 10 = 2
So 492450-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O2/c14-11-5-3-7-13-10(11)8-9-4-1-2-6-12(9)15-13/h8,12H,1-7H2
492450-55-2Relevant articles and documents
Environmentally benign, one-pot synthesis of pyrans by domino Knoevenagel/6π-electrocyclization in water and application to natural products
Jung, Ene Jin,Park, Byung Ho,Lee, Yong Rok
experimental part, p. 2003 - 2011 (2011/02/19)
In water medium, environmentally benign, facile, and efficient synthesis of pyrans was achieved in good yields by the reactions of a variety of cyclic 1,3-dicarbonyls with several α,β-unsaturated aldehydes. The key strategy was a formal [3+3] cycloaddition by domino Knoevenagel/6π- electrocyclization. This methodology was applied to the synthesis of biologically interesting pyranocoumarin, pyranoquinolinone, and pyranonaphthoquinone derivatives along with selected natural and non-natural products. The Royal Society of Chemistry 2010.
A Lewis acid-catalyzed formal [3 + 3] cycloaddition of α,β- unsaturated aldehydes with 4-hydroxy-2-pyrone, diketones, and vinylogous esters
Kurdyumov, Aleksey V.,Lin, Nan,Hsung, Richard P.,Gullickson, Glen C.,Cole, Kevin P.,Sydorenko, Nadiya,Swidorski, Jacob J.
, p. 191 - 193 (2007/10/03)
A Lewis acid-catalyzed formal cycloaddition of α,β-unsaturated aldehydes with 6-methyl-4-hydroxy-2-pyrone, 1,3-diketones, and vinylogous silyl esters is described here.
