96164-66-8 Usage
Uses
Used in Pharmaceutical Synthesis:
Hexyltrifluorosilane is used as a reagent for introducing the trifluorosilyl group into organic molecules, which is crucial in the synthesis of various pharmaceuticals. This modification can enhance the properties of the resulting compounds, such as solubility, stability, and bioavailability, making them more effective for medical applications.
Used in Agrochemical Production:
In the agrochemical industry, hexyltrifluorosilane is employed as a building block for the synthesis of compounds with specific properties, such as herbicides, insecticides, and fungicides. The trifluorosilyl group can improve the performance and selectivity of these agrochemicals, leading to more effective and environmentally friendly products.
Used in Material Science:
Hexyltrifluorosilane is utilized in the development of materials with unique properties, such as high thermal stability, low surface energy, and improved adhesion. The introduction of the trifluorosilyl group can enhance the performance of these materials, making them suitable for various applications, including coatings, adhesives, and sealants.
Used in Surface Coatings, Adhesives, and Sealants:
As an intermediate in the production of surface coatings, adhesives, and sealants, hexyltrifluorosilane contributes to the development of high-performance products with improved durability, adhesion, and resistance to environmental factors. The trifluorosilyl group can enhance the bonding strength and stability of these materials, making them ideal for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 96164-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,6 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 96164-66:
(7*9)+(6*6)+(5*1)+(4*6)+(3*4)+(2*6)+(1*6)=158
158 % 10 = 8
So 96164-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H13F3Si/c1-2-3-4-5-6-10(7,8)9/h2-6H2,1H3
96164-66-8Relevant academic research and scientific papers
Matsuhashi, Hayao,Asai, Satoshi,Hirabayashi, Kazunori,Hatanaka, Yasuo,Mori, Atsunori,Hiyama, Tamejiro
, p. 437 - 444 (1997)
A cross-coupling reaction of alkyltrifluorosilanes with aryl halides was achieved using a catalytic amount of tetrakis-(triphenylphosphine)palladium(0) and excess of tetrabutylammonium fluoride (TBAF) at 100°C with high chemoselectitvity. Functional groups like nitro, ketone carbonyl, and formyl tolerated the coupling conditions. Because potassium(18-crown-6) alkyltetrafluorosilicates also underwent a cross-coupling reaction in the presence of an additional molar amount of TBAF, the active species of the coupling reaction was assumed to be pentacoordinate silicates. TBAF in excess was considered to be required for trapping the tetrafluorosilane produced in the catalytic cycle of the cross-coupling reaction.
