13617-25-9 Usage
Uses
Used in Chemical Synthesis:
1-Methyl-2-phenethyltrichlorosilane is used as a reagent in chemical synthesis, specifically for the production of silane coupling agents. These agents are crucial for enhancing the adhesion between different materials, such as inorganic surfaces and organic polymers, and are widely used in the manufacturing of composite materials.
Used in Silicone Polymer Production:
In the silicone industry, 1-Methyl-2-phenethyltrichlorosilane serves as a crosslinking agent, which is essential for the formation of three-dimensional networks in silicone polymers. This role is vital for improving the mechanical properties and thermal stability of the resulting polymers, making them suitable for various applications, including sealants, adhesives, and elastomers.
Used in Surface Modification:
1-Methyl-2-phenethyltrichlorosilane is also utilized as a surface modifying agent for various materials, such as glass, metals, and ceramics. By altering the surface properties of these materials, it enhances their compatibility with other substances, improving adhesion, wettability, and overall performance in various applications.
Used in Coatings and Adhesives Industry:
1-Methyl-2-phenethyltrichlorosilane is employed as a component in the formulation of coatings and adhesives, where its reactivity and ability to form strong bonds with different substrates contribute to the development of high-performance products with improved durability and resistance to environmental factors.
Used in Electronic Industry:
In the electronics sector, 1-Methyl-2-phenethyltrichlorosilane is used in the fabrication of semiconductor devices and microelectronic components. Its role in surface modification and adhesion enhancement is crucial for the successful integration of various materials in these high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13617-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,1 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13617-25:
(7*1)+(6*3)+(5*6)+(4*1)+(3*7)+(2*2)+(1*5)=89
89 % 10 = 9
So 13617-25-9 is a valid CAS Registry Number.
13617-25-9Relevant academic research and scientific papers
Organofluorosilicates in Organic Synthesis. XVI. Synthesis of Organopentafluorosilicates via the Diels-Alder, Ene, and Friedel-Crafts Reaction. Their Transformations to Organic Halides and Alcohols
Tamao, Kohei,Yoshida, Jun-ichi,Akita, Munetaka,Sugihara, Yoshihiro,Iwahara, Takahisa,Kumada, Makoto
, p. 255 - 260 (2007/10/02)
Described herein are several representative examples of cleavage reactions of otherwise hardly accessible organopentafluorosilicates which are obtainable via the Diels-Alder reaction, ene reaction, and the Friedel-Crafts reaction of vinyl-, ethynyl-, or allyl-trichlorosilanes.The Diels-Alder reaction between vinyltrichlorosilane and o-xylylene generated in situ by debromination of α,α'-dibromo-o-xylene afforded (1,2,3,4-tetrahydro-2-naphthyl)-trichlorosilane which was converted to the corresponding silicate.The silicate reacted with NBS and MCPBA to give the respective bromide and alcohol.The Diels-Alder reaction between ethynyltrichlorosilane and methyl coumalate gave a mixture of meta and para isomers of methyl (trichlorosilyl)benzoate in the ratio of 55/45, the silicate of which reacted with NBS to give two positional isomers of methyl bromobenzoate.The electronic effect of the methoxycarbonyl group on the Si-C bond cleavage was small.The silicate derived from 4-octenyltrichlorosilane which was obtained by the ene reaction between vinyltrichlorosilane and 1-hexene afforded, upon treatment with NBS, 4-octenyl bromide in the ratio of E/Z=83/17.The sterically crowded neophylsilicate obtainable via the Friedel-Crafts reaction of 2-methyl-1-propenyltrichlorosilane with benzene underwent the cleavage reaction with NBS in methanol.Neophyl bromide was formed with CuBr2 in a low yield, no product being formed arising from rearrangement of the neophyl radical.
