1217863-25-6 Usage
Description
2-[(4-Chlorophenyl)dimethylsilyl]phenylmethanol is a chemical compound characterized by its molecular formula C17H19ClOSi. It is a white crystalline solid that is prominently utilized as a reagent in organic synthesis. 2-[(4-Chlorophenyl)dimethylsilyl]phenylmethanol features a phenyl ring with a chlorophenyl group and a dimethylsilyl group substitution, along with a hydroxyl group attached to the phenyl ring. Its structural composition endows it with versatile applications in different industries.
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-[(4-Chlorophenyl)dimethylsilyl]phenylmethanol is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to be a valuable component in the development of new drugs and agricultural chemicals, contributing to the enhancement of their efficacy and safety.
Used in Organic Synthesis:
As a reagent, 2-[(4-Chlorophenyl)dimethylsilyl]phenylmethanol is employed in organic synthesis to facilitate various chemical reactions. Its presence can help in the formation of desired products with improved yield and selectivity, making it a crucial component in the synthesis of complex organic molecules.
Used in the Production of Functional Materials:
2-[(4-Chlorophenyl)dimethylsilyl]phenylmethanol is also utilized in the production of functional materials, where its unique properties can be harnessed to create materials with specific characteristics. These materials can find applications in various fields, such as electronics, coatings, and adhesives, where their tailored properties can provide advantages over conventional materials.
Used as a Protecting Reagent:
In organic chemistry, 2-[(4-Chlorophenyl)dimethylsilyl]phenylmethanol serves as a protecting reagent to shield specific functional groups during chemical reactions. This protection is essential to prevent unwanted side reactions and ensure the selective formation of the desired product, ultimately leading to a more efficient and cleaner synthesis process.
Check Digit Verification of cas no
The CAS Registry Mumber 1217863-25-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,8,6 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1217863-25:
(9*1)+(8*2)+(7*1)+(6*7)+(5*8)+(4*6)+(3*3)+(2*2)+(1*5)=156
156 % 10 = 6
So 1217863-25-6 is a valid CAS Registry Number.
1217863-25-6Relevant articles and documents
Improved Hiyama cross-coupling reactions using HOMSi
Marcuccio, Sebastian M.,Epa, Ruwan,Moslmani, Maisa,Hughes, Andrew B.
, p. 7178 - 7181 (2012/01/14)
Various parameters in the Hiyama cross-coupling reaction of HOMSi reagents with ethyl bromobenzoate were studied. These included solvent, ligand, palladium source, and added water. DMF and THF were found to be excellent solvents. Palladium chloride was found to be the best palladium source and no added water was required. The use of tri-o-tolylphosphine as the ligand proved to be particularly effective.
