995-43-7

Usage

Uses

Used in Organic Synthesis:
Methyl-tri-n-butylsilane is used as a reagent in organic synthesis for the functionalization of silicon-based materials. Its unique structure allows for the attachment of various functional groups to silicon, enabling the creation of a wide range of organosilicon compounds with diverse applications.
Used in Cross-Coupling Reactions:
In the field of organic chemistry, Methyl-tri-n-butylsilane serves as a cross-coupling agent, facilitating the formation of carbon-carbon bonds. This property is particularly valuable in the synthesis of complex organic molecules, where the formation of specific carbon-carbon linkages is crucial for the desired molecular architecture.
Used in the Production of Specialty Chemicals:
Methyl-tri-n-butylsilane is employed in the production of specialty chemicals, such as silicones and silane coupling agents. These materials are used in various industries, including coatings, adhesives, sealants, and elastomers, due to their unique properties like heat resistance, water repellency, and adhesion to various substrates.
Used in the Semiconductor Industry:
In the semiconductor industry, Methyl-tri-n-butylsilane is utilized in the fabrication of silicon-based devices. Its ability to form stable bonds with silicon makes it a valuable component in the production of semiconductor materials and devices, contributing to the advancement of electronic and optoelectronic technologies.
Used in the Pharmaceutical Industry:
Methyl-tri-n-butylsilane is also used in the pharmaceutical industry for the synthesis of drug molecules that contain silicon. The incorporation of silicon into drug molecules can enhance their stability, solubility, and bioavailability, leading to improved therapeutic efficacy.

Upstream product

• 693-03-8 n-butyl magnesium bromide 
• 75-79-6 Methyltrichlorosilane 
• 109-72-8 n-butyllithium 
• 2031-67-6 Methyltriethoxysilan 
• 1578-31-0 tri(2-furyl)methylsilane 
• 102129-44-2 sodium bis(1,2-benzenediolato)methylsilicate 
• 1116-70-7 tri(n-butyl)aluminium 
• 106-98-9 1-butylene 
• 999-35-9 di-n-butylmethylsilane 
• 18147-23-4 butyl-dichloro-methyl-silane 
• 18143-64-1 butylmethylsilane 
• 19284-22-1 n-butylmethylchlorosilane 
• 996-07-6 dibutyl-chloro-methyl-silane 

Relevant academic research and scientific papers

PROCESS FOR THE STEPWISE SYNTHESIS OF SILAHYDROCARBONS

The invention relates to a process for the stepwise synthesis of silahydrocarbons bearing up to four different organyl substituents at the silicon atom, wherein the process includes at least one step a) of producing a bifunctional hydridochlorosilane by a redistribution reaction, selective chlorination of hydridosilanes with an ether/HCI reagent, or by selective chlorination of hydridosilanes with SiCI4, at least one step b) of submitting a bifunctional hydridochloromonosilane to a hydrosilylation reaction, at least one step c) of hydrogenation of a chloromonosilane, and a step d) in which a silahydrocarbon compound is obtained in a hydrosilylation reaction.

Synthesis of tetraalkylsilanes

This invention relates to a process for preparing tetrahydrocarbylsilane in high yield, comprising: a) forming a reaction mass from molten metal and trihydrocarbylaluminum, in an hydrocarbon solvent under an inert gas atmosphere; b) maintaining the reaction mass at a temperature in the range of from about 100° to about 130° C. for a period of time sufficient to form sodium tetrahydrocarbylaluminate; c) contacting the sodium tetrahydrocarbylaluminate with organotrihalosilane; and d) heating the contacted tetrahydrocarbylaluminate and organotrihalosilane to a temperature and for a period of time sufficient to form the tetrahydrocarbylsilane, wherein the tetrahydrocarbylaluminate and tetrahydrocarbylsilane are formed at a pressure of less than about 3000 KPa and wherein the hydrocarbyl group of the tetrahydrocarbyl silane is one or a mixture of hydrocarbyl groups having less than about 8 carbon atoms each.

Reactivity of Hypervalent Species: Reactions of Anionic Penta-Coordinated Silicon Complexes towards Nucleophiles

The reactivity of anionic penta-coordinated silicon complexes 4-O)2>-Na+ 1 with nucleophilic reagents has been studied. 1 can be reduced to organosilanes RSiH3 by metallic hydrides.Reactions with an excess of Grignard or organolithium reagents (R'MgX or R'Li) gave tetraorganosilanes RSiR'3.When only two molar equivalents of Grignard reagents (R'MgX) or lithium reagents (R'Li) are added to complexs 1 functional silanes RR'2SiX can be prepared.