2441-27-2 Usage
Uses
Used in Silicone Polymer Production:
Trichloro(1-chlorovinyl)silane serves as a crucial component in the synthesis of silicone polymers, which are valued for their thermal stability, chemical inertness, and hydrophobic properties. It is used as a monomer for the polymerization process, contributing to the formation of a wide range of silicone-based products.
Used in Chemical Synthesis:
In the chemical industry, trichloro(1-chlorovinyl)silane is utilized as a reagent or intermediate in various synthesis processes. Its high reactivity allows it to participate in numerous chemical reactions, making it a versatile compound for creating a variety of products.
Used in Coatings and Sealants:
trichloro(1-chlorovinyl)silane is also employed in the formulation of coatings and sealants, where its ability to form stable silicone polymers provides enhanced durability, water resistance, and adhesion properties.
Used in Adhesives:
Trichloro(1-chlorovinyl)silane contributes to the development of adhesives with strong bonding capabilities and resistance to environmental factors, such as moisture and temperature fluctuations.
Used in Electronic Applications:
In the electronics industry, the compound is used in the creation of silicone-based materials for insulation, encapsulation, and as a component in the manufacturing of semiconductor devices, taking advantage of its thermal and chemical stability.
Used in Textile and Paper Processing:
Trichloro(1-chlorovinyl)silane is utilized in the textile and paper industries for water-repellent and soil-release finishes, leveraging its ability to form durable, hydrophobic coatings on fibers and paper surfaces.
Used in Cosmetics and Personal Care:
In cosmetics and personal care products, the compound is used to create silicone-based emollients, providing a smooth, non-greasy feel and improving the spreadability of formulations.
Used in Medical Applications:
In the medical field, trichloro(1-chlorovinyl)silane is employed in the development of silicone-based materials for use in implants, medical devices, and drug delivery systems, capitalizing on its biocompatibility and stability.
Each application of trichloro(1-chlorovinyl)silane leverages its unique chemical properties to fulfill specific needs within various industries, underscoring its importance and versatility in modern chemical manufacturing and product development.
Check Digit Verification of cas no
The CAS Registry Mumber 2441-27-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2441-27:
(6*2)+(5*4)+(4*4)+(3*1)+(2*2)+(1*7)=62
62 % 10 = 2
So 2441-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H2Cl4Si/c1-2(3)7(4,5)6/h1H2
2441-27-2Relevant academic research and scientific papers
Polyfluoroalkyl derivatives of silicon. Part XIII. Preparation and pyrolysis of trifluoro(halogenovinyl)silanes and (1-fluoro-2-halogenoethyl)trihalogenosilanes
Haszeldine, Robert N.,Pool, Colin R.,Tipping, Anthony E.
, p. 2177 - 2181 (2007/10/12)
Treatment of 1-chloro-2-fluoroethyl- or 1,2-dichloroethyl-trichlorosilane with quinoline gives trichloro(1-chlorovinyl)silane; trichloro(1,2-dibromoethyl)silane dehydrohalogenates similarly. In contrast 2-chloro-1-fluoro-ethyl- and 1,2-difluoroethyl-trichlorosilane give vinyl fluoride under comparable conditions. Both 1-chlorovinyl-and 1-bromovinyl-trifluorosilane, prepared from the trichlorosilyl analogues, decompose slowly at 280°C to afford acetylene and tetrahalogenosilanes via the suspected intermediacy of the alkylidenecarbene CH2:C:. Pyrolysis of (2-chloro-1-fluoroethyl)trifluorosilane gives vinyl chloride via a carbene intermediate, but the trichlorosilyl analogue yields the rearrangement compound dichloro(1,2-dichloroethyl)fluorosilane. 1,2-Difluoroethyl-trifluorosilane and -trichlorosilane both decompose via a non-carbene mechanism involving β elimination.
