18290-60-3 Usage
Uses
Used in Chemical Synthesis:
[2-(3-Cyclohexenyl)ethyl]trichlorosilane is used as a precursor in the synthesis of various organosilicon compounds, leveraging its reactivity to form a range of silicon-containing materials.
Used in Silicone Polymer Production:
In the polymer industry, [2-(3-Cyclohexenyl)ethyl]trichlorosilane serves as a crosslinking agent, crucial for the production of silicone polymers, which are known for their thermal stability, flexibility, and resistance to environmental degradation.
Used in Surface Functionalization:
[2-(3-CYCLOHEXENYL)ETHYL]TRICHLOROSILANE is utilized as a reagent in the functionalization of surfaces, where its ability to form covalent bonds with surfaces can alter their properties for specific applications, such as improving adhesion or introducing new functionalities.
Used in Pharmaceutical and Agrochemical Synthesis:
[2-(3-Cyclohexenyl)ethyl]trichlorosilane is employed as an intermediate in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides by providing a versatile route to incorporate silicon-containing moieties into these molecules.
Used in Research and Development:
In the field of research and development, [2-(3-Cyclohexenyl)ethyl]trichlorosilane is used to explore new chemical reactions and mechanisms, as well as to develop novel materials with improved properties, such as enhanced thermal stability or specific catalytic activities.
Check Digit Verification of cas no
The CAS Registry Mumber 18290-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,9 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18290-60:
(7*1)+(6*8)+(5*2)+(4*9)+(3*0)+(2*6)+(1*0)=113
113 % 10 = 3
So 18290-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H13Cl3Si/c9-12(10,11)7-6-8-4-2-1-3-5-8/h1-2,8H,3-7H2
18290-60-3Relevant academic research and scientific papers
Trichlorosilyl groups containing organochlorosilanes and their preparation methods by the double-silylation of olefins with trichlorosilane
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Page 4, (2008/06/13)
The present invention provides organosilicon compounds containing two trichlorosilyl groups and their preparation methods. Organosilicon compounds of formula II are prepared by reacting linear chain or cyclic olefins of formula I with trichlorosilane in the presence of quaternary organophosphonium salt as a catalyst.R1—HC=CH—R2??(I) 1In formulas I and II, R1 and R2 may be identical or different and represent a hydrogen atom, a linear or a cyclic C1-C8 alkyl, a linear or a cyclic C1-C8 alkenyl, benzyl, phenyl, a C1-C8 alkyl substituted phenyl group, two functional groups between R1 and R2 may be covalently bonded to form a C4-C8 ring with or without a carbon-carbon double bond.
Hydrosilylation of 4-vinyl-1-cyclohexene
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, (2008/06/13)
By reacting 4-vinyl-1-cyclohexene with a hydrogenchlorosilane compound in the presence of a platinum catalyst to give a reaction solution containing a monosilyl compound, removing the residual 4-vinyl-1-cyclohexene and isomers thereof from the reaction solution, and reacting the monosilyl compound again with the hydrogenchlorosilane compound, an organic silicon compound in which the two double bonds in 4-vinyl-1-cyclohexene have been hydrosilylated is produced in high yields.
