18406-93-4

Usage

Uses

Used in Organic Synthesis:
Silane, (2-methyl-2,5-cyclohexadiene-1,4-diyl)bis[trimethylis used as a reagent in organic synthesis for its ability to participate in various chemical reactions, facilitating the formation of new silicon-containing compounds with potential applications in different industries.
Used in Materials Science:
In the field of materials science, Silane, (2-methyl-2,5-cyclohexadiene-1,4-diyl)bis[trimethylis utilized as a precursor for developing new materials with enhanced properties. Its unique structure allows for the creation of materials with improved characteristics, such as thermal stability, mechanical strength, or specific chemical functionalities.
Used in Silicone Production:
Silane, (2-methyl-2,5-cyclohexadiene-1,4-diyl)bis[trimethylplays a role in the production of silicones, which are a class of polymers known for their wide range of applications, including sealants, adhesives, lubricants, and medical devices. Silane, (2-methyl-2,5-cyclohexadiene-1,4-diyl)bis[trimethylcontributes to the synthesis process, enabling the creation of silicones with tailored properties for specific uses.
Used in Research and Development:
In research and development, Silane, (2-methyl-2,5-cyclohexadiene-1,4-diyl)bis[trimethylis employed as a model compound to study the properties and reactivity of silanes. This helps in understanding the fundamental chemistry of these compounds and exploring new applications and uses in various fields.

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 108-88-3 toluene 

Downstream Products

• 7722-84-1 dihydrogen peroxide 
• 75-77-4 chloro-trimethyl-silane 
• 20395-25-9 1,1,3-trichloropropane 

Relevant academic research and scientific papers

BIS(TRIMETHYLSILYL) SIX-MEMBERED RING SYSTEMS AND RELATED COMPOUNDS AS REDUCING AGENTS FOR FORMING LAYERS ON A SUBSTRATE

A first compound having an atom in an oxidized state is reacted with a bis(trimethylsilyl) six-membered ring system or related compound to form a second compound having the atom in a reduced state relative to the first compound. The atom in an oxidized state is selected from the group consisting of Groups 2-12 of the Periodic Table, the lanthanides, As, Sb, Bi, Te, Si, Ge, Sn, and Al.

The Electrochemical Reductive Trimethylsilylation of Aryl Chlorides: A Good Route to Aryltrimethylsilanes and a Novel Route to Tris(trimethylsilyl)cyclohexadienes

The electroreductive trimethylsilylation of aryl chlorides R-C6H4Cl (R = H, o-Me, m-Me, p-Me) can be controlled so as to give, in good yields, either the corresponding aryltrimethylsilanes (products of the reduction of the carbon-chlorine bond) or mixtures of cis- and trans-tris(trimethylsilyl)cyclohexa-1,3(or 1,4)-dienes (products of the successive reduction of the carbon-chlorine bond and the partial reduction of the aromatic ring).Which of the two products is formed depends upon how much electricity is passed during the constant current electrolysis, in a one-compartment cell equipped with a sacrificial aluminum anode, of an aryl chloride in 80:20 THF/HMPA solution that also contains Et4NBF4 as the supporting electrolyte and excess Me3SiCl.The electroreductive trimethylsilylation of phenyltrimethylsilane gave, in 62percent yield, a mixture of three 3,5,6-tris(trimethylsilyl)cyclohexa-1,3-dienes, of which the trans, pseudo a-a isomer constituted 89percent.Such products cannot be obtained by the chemoreductive trimethylsilylation of phenyltrimethylsilane.The electroreductive trimethylsilylation of benzene and toluene produced the corresponding bis(trimethylsilyl)cyclohexa-1,4-dienes.The regio- and stereochemical outcomes of the electroreductive trimethylsilylation of the various substrates can be explained in terms of the electronic and steric effects of the substituents originally attached to the aromatic ring and the steric effects of the trimethylsilyl groups that are subsequently attached.