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115262-00-5 | (Chlorodifluoromethyl)trimethylsilane

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(Chlorodifluoromethyl)trimethylsilane (CFMTS) is a chemical compound with a wide range of practical applications. It is a colorless, volatile liquid with a strong odor that is used in a variety of fields such as pharmaceuticals, electronics, and materials science. CFMTS is a useful reagent in organic synthesis due to i...

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CAS:115262-00-5 | (Chlorodifluoromethyl)trimethylsilane ,Description

(Chlorodifluoromethyl)trimethylsilane (CFMTS) is a chemical compound with a wide range of practical applications. It is a colorless, volatile liquid with a strong odor that is used in a variety of fields such as pharmaceuticals, electronics, and materials science. CFMTS is a useful reagent in organic synthesis due to its ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds. It is also used as a solvent for various organic compounds and as a catalyst for various reactions. CFMTS is an important intermediate for the production of various fluorinated compounds and can be used as a starting material for the synthesis of various organofluorines.
 

Scientific Research Applications

 

  • Dielectric Thin Film Deposition: Trimethylsilane-based PECVD processes, using materials like (Chlorodifluoromethyl)trimethylsilane, can deposit dielectric thin films. These films are used in advanced device multilevel metal interconnection schemes, improving circuit performance (Loboda, 1999).
  • Synthesis of Gem-Difluoroolefins: (Chlorodifluoromethyl)trimethylsilane, combined with triphenylphosphine, synthesizes gem-difluoroolefins from carbonyl compounds. These compounds are precursors for organic synthesis and act as bioisosteres for enzyme inhibitors (Wang, Li, Ni, & Hu, 2014).
  • Organic Chemistry: (Chlorodifluoromethyl)trimethylsilane is used to assemble compounds bearing chlorodifluoromethyl groups from organozinc chlorides and sulfuryl chloride (Smirnov, Maslov, Levin, Struchkova, & Dilman, 2014).
  • Gold-Catalyzed Oxidative Coupling Reactions: Aryltrimethylsilanes, including (Chlorodifluoromethyl)trimethylsilane, are used in gold-catalyzed oxidative coupling reactions. This process demonstrates an intramolecular electrophilic aromatic substitution mechanism (Brenzovich, Brazeau, & Toste, 2010).
  • Chemical Vapor Deposition (CVD) Chemistry: The effect of (Chlorodifluoromethyl)trimethylsilane pressure on CVD chemistry was studied. It plays a role in the formation of methane and other hydrocarbon molecules during the CVD process (Toukabri & Shi, 2013).
  • Organometallic Synthesis: Various trimethylsilanes, including (Chlorodifluoromethyl)trimethylsilane, are utilized as carbanion equivalents for synthesis in organometallic chemistry (Das & O’Shea, 2014).
  • Surface Chemistry Studies: Studies on trimethylsilane-dosed surfaces provide insights into electron beam effects and surface chemistry, which are crucial for understanding surface reactions and coatings (Wang et al., 1995).

More Information

Product Name :(Chlorodifluoromethyl)trimethylsilane
CAS No. :115262-00-5Molecular Weight :158.65
MDL No. :MFCD20486786Purity/ Specification : 
Molecular Formula :C4H9ClF2SiStorage :Inert atmosphere,2-8°C
Boiling Point :-  
GHS Pictogram : 
Signal Word :DangerPrecautionary Statements :P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
UN# :1993Class :3
Hazard Statements :H225Packing Group :

 

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