69883-97-2 Usage
General Description
"(10Z)-3-hydroxy-2a,6,10-trimethyl-3-(1-methylethenyl)-2a,3,5,6,11a,11b-hexahydro-2H-6,9-epoxy-1,4-dioxacyclodeca[cd]pentalene-2,7(4aH)-dione" is a complex organic compound containing a cyclic structure with multiple functional groups. It is a dione, meaning it contains two ketone groups, and also features a hydroxyl group and an epoxy group. The compound also contains multiple methyl and ethenyl (vinyl) groups. As a result of these structural features, it is likely to exhibit a range of chemical and biological activities, and may have potential applications in various fields including pharmaceuticals, materials science, and organic synthesis. Further study and analysis would be necessary to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 69883-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,8 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69883-97:
(7*6)+(6*9)+(5*8)+(4*8)+(3*3)+(2*9)+(1*7)=202
202 % 10 = 2
So 69883-97-2 is a valid CAS Registry Number.
69883-97-2Relevant articles and documents
One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent
Sass, Daiane Cristina,Gomes Heleno, Vladimir Constantino,Callegari Lopes, Jo?o Luis,Constantino, Mauricio Gomes
, p. 3877 - 3880 (2008)
The conversion of a furanoheliangolide structure (15-deoxygoyazensolide) into an eremantholide one (eremantholide C) was achieved by tandem hydride conjugate addition-intramolecular carbanion addition using Stryker's reagent.
Solvent effect in reactions using strykers reagent
Sass, Daiane Cristina,Heleno, Vladimir Constantino Gomes,Cavalcante, Simone,Da Silva Barbosa, Jader,Soares, Ana Carolina Ferreira,Constantino, Mauricio Gomes
, p. 9374 - 9378 (2013/01/15)
The solvent has a significant influence in the rate of reactions promoted by Strykers reagent. The reactions performed in THF were, in most cases, faster than in toluene.
