804548-75-2 Usage
Uses
Used in Organic Synthesis:
2(3H)-Furanone, 4-butyldihydro-3-(1-hydroxy-2-methylpropyl)-5-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]-, (3S,4R,5R)is used as an intermediate in organic synthesis for the production of various complex organic molecules, leveraging its unique structure and functional groups.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2(3H)-Furanone, 4-butyldihydro-3-(1-hydroxy-2-methylpropyl)-5-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]-, (3S,4R,5R)may be utilized as a building block for the development of new drugs, given its chiral nature and diverse functional groups that can be exploited for medicinal chemistry applications.
Used as a Flavor or Fragrance Ingredient:
2(3H)-Furanone, 4-butyldihydro-3-(1-hydroxy-2-methylpropyl)-5-[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]-, (3S,4R,5R)could be employed as a flavor or fragrance ingredient in the food, beverage, or cosmetics industries, capitalizing on its potential aromatic properties and the ability to impart unique scents or tastes.
Check Digit Verification of cas no
The CAS Registry Mumber 804548-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,4,5,4 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 804548-75:
(8*8)+(7*0)+(6*4)+(5*5)+(4*4)+(3*8)+(2*7)+(1*5)=172
172 % 10 = 2
So 804548-75-2 is a valid CAS Registry Number.
804548-75-2Relevant academic research and scientific papers
Conjugate addition of organocopper reagents to γ-alkoxybutenolides and application to the synthesis of non-racemic alkyl cyclopentenones
Robertson, Jeremy,Menant, Morgan,Ford, Rhonan,Bell, Stephen
, p. 2988 - 2997 (2007/10/03)
Simple organocopper reagents are shown to undergo anti-stereoselective 1,4-addition to menthyloxy-substituted lactone 1 in the presence of BF 3·OEt2; the Lewis acid causes partial epimerisation of the acetal centre after conjugate addition. Enolate alkylation of the adducts leads to di- and trisubstituted lactones that are converted, in favourable cases, into di- and trisubstituted cyclopentenones.
