804548-75-2 Usage
General Description
The chemical compound 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 a complex organic compound with a furanone ring and multiple hydroxyl and alkyl groups. It is a chiral molecule with stereochemistry defined by the (3S,4R,5R) configuration. Its structure includes a butyl group, a cyclohexyl ring with a methyl and isopropyl group, and a furanone ring linked to a hydroxyisopropyl group. 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 have applications in organic synthesis, pharmaceuticals, or as a flavor or fragrance ingredient, but further research and testing would be needed to determine its specific uses and properties.
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 articles and documents
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.