109629-99-4 Usage
Uses
Used in Silicone Rubber and Adhesives Production:
CyclohexyldiethoxyMethylsilane is used as a crosslinking agent for improving the performance and properties of silicone rubbers and adhesives. Its reactivity and low viscosity make it an effective ingredient in these applications.
Used in Coatings Industry:
In the coatings industry, CyclohexyldiethoxyMethylsilane is used as an additive to enhance the adhesion, flexibility, and durability of coatings. Its ability to improve these properties makes it a valuable component in the formulation of various types of coatings.
Used in Sealants Industry:
CyclohexyldiethoxyMethylsilane is also utilized in the production of sealants, where it serves to boost the adhesion, flexibility, and durability of the sealant materials, ensuring their effectiveness in various sealing applications.
Used in Specialized Silicone Products:
CyclohexyldiethoxyMethylsilane finds application in the development of specialized silicone products, where its crosslinking properties contribute to the creation of materials with improved performance characteristics, tailored to specific industrial needs.
Check Digit Verification of cas no
The CAS Registry Mumber 109629-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,6,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 109629-99:
(8*1)+(7*0)+(6*9)+(5*6)+(4*2)+(3*9)+(2*9)+(1*9)=154
154 % 10 = 4
So 109629-99-4 is a valid CAS Registry Number.
109629-99-4Relevant academic research and scientific papers
Wiesenfeldt, Mario P.,Knecht, Tobias,Schlepphorst, Christoph,Glorius, Frank
, p. 8297 - 8300 (2018)
We report a method to convert readily available silylated arenes into silylated saturated carbo- and heterocycles by arene hydrogenation. The scope includes alkoxy- and halosilyl substituents. Silyl groups can be derivatized into a plethora of functionalities and find application in organic synthesis, materials science, and pharmaceutical, agrochemical, and fragrance research. However, silylated saturated (hetero-) cycles are difficult to access with current technologies. The yield of the hydrogenation depends on the amount of the silica gel additive. This silica effect also enables a significant improvement of a previously disclosed method for the hydrogenation of highly fluorinated arenes (e.g., to all-cis-C6H6F6).
