358-60-1 Usage
Uses
Used in Silicone Rubber Production:
Triethoxyfluorosilane is used as a crosslinking agent for enhancing the strength and durability of silicone rubber. Its ability to form stable bonds within the rubber matrix contributes to the creation of high-performance silicone products with improved mechanical properties.
Used in Surface Modification of Glass and Metal:
In the glass and metal industries, triethoxyfluorosilane is utilized as a surface modifier. It helps improve the adhesion, wettability, and overall performance of these materials by altering their surface properties, leading to better integration with other substances or coatings.
Used as an Adhesion Promoter in Various Industrial Applications:
Triethoxyfluorosilane is employed as an adhesion promoter to improve the bonding between different materials. Its reactivity allows it to form strong chemical bonds with various substrates, ensuring a robust and durable connection in applications such as coatings, adhesives, and sealants.
Used in Coatings Industry:
Triethoxyfluorosilane is used as a component in the formulation of coatings to enhance their adhesion to various surfaces, including glass, metal, and plastics. This results in coatings with improved durability, resistance to wear, and overall performance.
Used in Adhesives and Sealants Industry:
In the adhesives and sealants industry, triethoxyfluorosilane is used to improve the bonding strength and flexibility of these products. Its ability to form strong chemical bonds with different substrates ensures a reliable and long-lasting adhesion in various applications, such as automotive, construction, and electronics.
Used in Electronic Industry:
Triethoxyfluorosilane is utilized in the electronic industry for its ability to improve the adhesion and performance of electronic components and materials. It is particularly useful in the fabrication of semiconductor devices, where its surface-modifying properties can enhance the performance and reliability of the devices.
Check Digit Verification of cas no
The CAS Registry Mumber 358-60-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 358-60:
(5*3)+(4*5)+(3*8)+(2*6)+(1*0)=71
71 % 10 = 1
So 358-60-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H15FO3Si/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3
358-60-1Relevant academic research and scientific papers
Cleavage of the C-Si bond in trifluoro(phenyl)silane with aliphatic alcohols
Voronkov,Boyarkina,Gebel',Albanov,Basenko
, p. 1927 - 1929 (2008/02/03)
Trifluoro(phenyl)silane reacts with aliphatic alcohols under reflux. The reaction involves not only Si-F bond cleavage to form ethoxyfluoro(phenyl) silanes, but also C-Si bond cleavage to form benzene and alkoxyfluoro- and tetraalkoxysilanes. The formation of the latter products was proved by 19F and 29Si NMR spectroscopy and also by model disproportionation reactions of trifluoro(phenyl)silane with trimethoxy-(phenyl)-, tetramethoxy-, or tetraethoxysilanes.
A convenient preparation of pentafluorophenyl( fluoro) silanes: Reactivity of pentafluorophenyltrifluorosilane
Frohn,Giesen,Klose,Lewin,Bardin
, p. 155 - 164 (2007/10/02)
Pentafluorophenyl(fluoro)silanes (C6F5)nSiF4-n (n = 1, 2) were prepared from the corresponding ethoxysilanes by sequential chlorodeethoxylation with SOCl2 and fluoridation of chlorosilanes with SbF3. The conversion of C6F5Si(OEt)3 and C6F5SiCl3 into C6F5SiF3 with anhydrous HF was described. Some reactions of C6F5SiF3 with electrophiles and nucleophiles were studied.
