69883-97-2 Usage
Uses
Used in Pharmaceutical Applications:
(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 can be used as a pharmaceutical agent due to its complex structure and potential biological activities. Its hydroxyl and epoxy groups may allow for interactions with biological targets, and its ketone groups could be involved in metabolic processes. Further research would be needed to determine the specific therapeutic applications of (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.
Used in Materials Science:
In the field of materials science, (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 may be utilized in the development of new materials with unique properties. Its cyclic structure and functional groups could contribute to the formation of novel polymers or composites with specific characteristics, such as enhanced stability or reactivity.
Used in Organic Synthesis:
(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 can also be employed as a building block or intermediate in organic synthesis. Its diverse functional groups and structural features make it a potentially valuable component in the synthesis of more complex organic molecules, which could have applications in various industries, such as pharmaceuticals, agrochemicals, or specialty chemicals.
Note: The specific applications and industries mentioned above are hypothetical and provided as examples based on the compound's structural features. Further research and development would be necessary to fully explore and validate the potential uses of (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.
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 academic research and scientific papers
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.
Identification of a Covalent Importin-5 Inhibitor, Goyazensolide, from a Collective Synthesis of Furanoheliangolides
Barluenga, Sofia,Liu, Weilong,Loewith, Robbie,Patouret, Rémi,Plank, Michael,Winssinger, Nicolas
, p. 954 - 962 (2021/06/28)
Sesquiterpenes are a rich source of covalent inhibitors with a long history in traditional medicine and include several important therapeutics and tool compounds. Herein, we report the total synthesis of 16 sesquiterpene lactones via a build/couple/pair strategy, including goyasensolide. Using an alkyne-tagged cellular probe and proteomics analysis, we discovered that goyazensolide selectively targets the oncoprotein importin-5 (IPO5) for covalent engagement. We further demonstrate that goyazensolide inhibits the translocation of RASAL-2, a cargo of IPO5, into the nucleus and perturbs the binding between IPO5 and two specific viral nuclear localization sequences.
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.
Selectivity in reduction of natural furanoheliangolides with Stryker's reagent
Sass, Daiane C.,Heleno, Vladimir C. G.,Morais, Gustavo O.,Lopes, Joao L. C.,Lopes, Norberto P.,Constantino, Mauricio G.
experimental part, p. 6148 - 6153 (2011/10/08)
Reduction of the natural sesquiterpene lactones furanoheliangolides with Stryker's reagent is an effective process for producing eremantholides through a biomimetic pathway. Other reduction products are also formed. Oxygenated functions at C-15 of the fur
