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223668-64-2 | Trimethoxy(pentafluorophenyl)silane

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Trimethoxy(pentafluorophenyl)silane, also known as TMPS, is a silane derivative with a pentafluorophenyl group attached to a methoxy group. It is used in a variety of applications, such as in organic synthesis, as a reagent for surface modification, as a catalyst for polymerization, and as a precursor for other organos...

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CAS:223668-64-2 | Trimethoxy(pentafluorophenyl)silane ,Description

Trimethoxy(pentafluorophenyl)silane, also known as TMPS, is a silane derivative with a pentafluorophenyl group attached to a methoxy group. It is used in a variety of applications, such as in organic synthesis, as a reagent for surface modification, as a catalyst for polymerization, and as a precursor for other organosilicon compounds. TMPS is also used for the synthesis of polymers, for the production of nanomaterials, and for the modification of surfaces.
 

Scientific Research Application

Trimethoxy(pentafluorophenyl)silane is used in a variety of scientific research applications, including organic synthesis, surface modification, and polymerization. It is also used as a precursor for other organosilicon compounds. Trimethoxy(pentafluorophenyl)silane has been used in the synthesis of polymers, for the production of nanomaterials, and for the modification of surfaces. It has also been used in the synthesis of polymers for the production of nanomaterials, and for the modification of surfaces.
 

Mechanism of Action

Trimethoxy(pentafluorophenyl)silane reacts with a variety of organic compounds, including alcohols, amines, and carboxylic acids. The reaction is typically catalyzed by tertiary amines, such as triethylamine, or by a base, such as sodium hydroxide. The reaction proceeds via an SN2 mechanism, in which the silicon atom of the Trimethoxy(pentafluorophenyl)silane molecule is replaced by the organic compound.
 

Biochemical and Physiological Effects

Trimethoxy(pentafluorophenyl)silane has no known biochemical or physiological effects. It is not known to be toxic or hazardous to humans or animals.
 

Advantages and Limitations for Lab Experiments

The main advantage of using Trimethoxy(pentafluorophenyl)silane in laboratory experiments is its low cost and availability. It is also relatively easy to handle and store, and is non-toxic and non-hazardous. However, Trimethoxy(pentafluorophenyl)silane is a relatively volatile compound, and can easily evaporate if not stored properly.
 

Future Directions

In the future, Trimethoxy(pentafluorophenyl)silane could be used in the development of new catalysts and polymerization processes. It could also be used in the synthesis of new materials, such as nanomaterials, for use in medical and industrial applications. Additionally, Trimethoxy(pentafluorophenyl)silane could be used in the development of new surface modification techniques, such as self-assembly and microfluidic techniques. Finally, Trimethoxy(pentafluorophenyl)silane could be used in the development of new methods for the synthesis of organosilicon compounds.

More Information

Product Name :Trimethoxy(perfluorophenyl)silane
CAS No. :223668-64-2Molecular Weight :288.24
MDL No. :MFCD04039205Purity/ Specification : 
Molecular Formula :C9H9F5O3SiStorage :Inert atmosphere,Room Temperature
Boiling Point :-  
GHS Pictogram : 
Signal Word :WarningPrecautionary Statements :P501-P210-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313-P403+P235
UN# :N/AClass :N/A
Hazard Statements :H315-H319-H227Packing Group :N/A

 

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