268736-19-2 Usage
Uses
Used in Organic Synthesis:
2,5-Cyclohexadien-1-one, 4-[1-(1,1-dimethylethoxy)-2-iodoethoxy]-4-methylis used as a reactive intermediate for the synthesis of various organic compounds. Its unique structure allows it to participate in a wide array of chemical reactions, making it a valuable component in the creation of new molecules with specific properties.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,5-Cyclohexadien-1-one, 4-[1-(1,1-dimethylethoxy)-2-iodoethoxy]-4-methylis used as a key building block for the development of novel drugs. Its reactivity and solubility properties enable the compound to be incorporated into drug molecules, potentially leading to the discovery of new therapeutic agents with improved efficacy and selectivity.
Used in Material Science:
2,5-Cyclohadien-1-one, 4-[1-(1,1-dimethylethoxy)-2-iodoethoxy]-4-methylis utilized in material science for the development of new materials with unique properties. Its ability to participate in various chemical reactions allows it to be integrated into the synthesis of advanced materials with applications in areas such as electronics, coatings, and adhesives.
Used in the Preparation of Complex Molecules:
2,5-Cyclohexadien-1-one, 4-[1-(1,1-dimethylethoxy)-2-iodoethoxy]-4-methylserves as a valuable building block for the preparation of more complex molecules with diverse functionalities. Its unique structure and reactivity make it an ideal candidate for the synthesis of advanced compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 268736-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,8,7,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 268736-19:
(8*2)+(7*6)+(6*8)+(5*7)+(4*3)+(3*6)+(2*1)+(1*9)=182
182 % 10 = 2
So 268736-19-2 is a valid CAS Registry Number.
268736-19-2Relevant academic research and scientific papers
Villar, Felix,Equey, Olivier,Renaud, Philippe
, p. 1061 - 1063 (2000)
Desymmetrization of 1,4-dien-3-ols and related compounds via Ueno-Stork radical cyclizations is reported. The stereochemistry of the cyclization is controlled by the acetal center. Excellent stereocontrol at C(4) and C(5) of the newly formed tetrahydrofuran rings is observed. Use of a chiral auxiliary allows the preparation of enantiomerically pure material. The utility of this method has been demonstrated by achieving a short synthesis of (+)-eldanolide, the pheromone of the male African sugarcane stem borer Eldana saccharina.
Highly stereoselective radical cyclization of haloacetals controlled by the acetal center
Villar, Felix,Kolly-Kovac, Tanja,Equey, Olivier,Renaud, Philippe
, p. 1566 - 1577 (2007/10/03)
A systematic investigation of radical haloacetal cyclizations (Ueno-Stork reaction) where the acetal center is the unique stereogenic element is reported. This highly diastereoselective reaction can be used for the preparation of polysubstituted tetrahydrofurans and γ-lactones. We report herein the full experimental details of reactions where up to three new chiral centers are created. To demonstrate the potential of this approach, short syntheses of (+)-eldanolide and of tricyclic acetals related to biologically active lignans have been achieved.
