53883-59-3 Usage
Uses
Used in Adhesives and Sealants Industry:
m-(TRIFLUOROMETHYL)PHENYLTRIMETHOXYSILANE is used as an adhesion promoter for improving the bond strength between organic and inorganic materials. Its application in this industry is crucial for the production of high-performance adhesives and sealants that offer enhanced durability and reliability in various applications.
Used in Coatings Industry:
In the coatings industry, m-(TRIFLUOROMETHYL)PHENYLTRIMETHOXYSILANE is utilized as a coupling agent to enhance the adhesion of coatings to various substrates. This results in coatings with improved durability, resistance to environmental factors, and overall performance.
Used in Surface Modification:
m-(TRIFLUOROMETHYL)PHENYLTRIMETHOXYSILANE is employed as a surface modifier to alter the properties of materials, such as improving their hydrophobicity, increasing their resistance to wear, or enhancing their compatibility with other materials. This application is vital in various industries, including automotive, aerospace, and electronics, where material performance is critical.
Used in Pharmaceutical Synthesis:
As a versatile chemical compound, m-(TRIFLUOROMETHYL)PHENYLTRIMETHOXYSILANE is used in the synthesis of pharmaceuticals and other organic compounds. Its reactivity allows for the creation of new drug molecules with potential therapeutic applications.
Used in Glass and Plastic Composites Production:
In the production of glass and plastic composites, m-(TRIFLUOROMETHYL)PHENYLTRIMETHOXYSILANE is used as a key component to improve the interfacial adhesion between the organic and inorganic phases. This results in composites with enhanced mechanical properties and overall performance.
Check Digit Verification of cas no
The CAS Registry Mumber 53883-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,8 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53883-59:
(7*5)+(6*3)+(5*8)+(4*8)+(3*3)+(2*5)+(1*9)=153
153 % 10 = 3
So 53883-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H13F3O3Si/c1-14-17(15-2,16-3)9-6-4-5-8(7-9)10(11,12)13/h4-7H,1-3H3
53883-59-3Relevant academic research and scientific papers
Direct Hiyama Cross-Coupling of (Hetero)arylsilanes with C(sp2)-H Bonds Enabled by Cobalt Catalysis
Lu, Ming-Zhu,Ding, Xin,Shao, Changdong,Hu, Zhengsong,Luo, Haiqing,Zhi, Sanjun,Hu, Huayou,Kan, Yuhe,Loh, Teck-Peng
supporting information, p. 2663 - 2668 (2020/03/30)
We report a chelation-assisted C-H arylation of various indoles with sterically and electronically diverse (hetero)arylsilanes enabled by cost-effective Cp*-free cobalt catalysis. Key to the success of this strategy is the judicious choice of copper(II) fluoride as a bifunctional sliane activator and catalyst reoxidant. This methodology features a broad substrate scope and good functional group compatibility. The synthetic versatility of this protocol has been highlighted by the gram-scale synthesis and late-stage diversification of biologically active molecules.
Directed palladium(II)-catalyzed intermolecular anti-markovnikov hydroarylation of unactivated alkenes with (hetero)arylsilanes
Lu, Ming-Zhu,Loh, Teck-Peng,Luo, Haiqing,Hu, Zhengsong,Shao, Changdong,Kan, Yuhe
supporting information, p. 9022 - 9028 (2020/12/02)
We describe herein a regioselective palladium(II)catalyzed intermolecular hydroarylation of unactivated aliphatic alkenes with electronically and sterically diverse (hetero)arylsilanes under redox-neutral conditions. A removable bidentate 8-amino-quinoline auxiliary was readily employed to dictate the regioselectivity, prevent β-hydride elimination, and facilitate protodepalladation. This silicon-based protocol features a broad substrate scope with excellent functional group compatibility and enables an expeditious route to a variety of γ-aryl butyric acid derivatives in good yields with exclusive anti-Markovnikov selectivity.
