100694-07-3

Usage

Uses

Used in Organic Synthesis:
Lithium, [bis(2,4,6-trimethylphenyl)silyl]is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its high reactivity and selectivity make it a valuable tool in creating complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Lithium, [bis(2,4,6-trimethylphenyl)silyl]is used as a key reagent for the synthesis of various drugs. Its ability to form carbon-carbon and carbon-heteroatom bonds facilitates the production of complex pharmaceutical compounds.
Used in Agrochemical Production:
Lithium, [bis(2,4,6-trimethylphenyl)silyl]is also utilized in the agrochemical industry for the synthesis of pesticides and other agrochemicals. Its reactivity and selectivity contribute to the development of effective and targeted agrochemical products.
Used in Materials Science:
In the field of materials science, Lithium, [bis(2,4,6-trimethylphenyl)silyl]is employed in the synthesis of advanced materials with specific properties. Its role in forming carbon-carbon and carbon-heteroatom bonds allows for the creation of materials with tailored characteristics for various applications.

Upstream product

• 50490-74-9 chloro-di-(2,4,6-trimethylphenyl)silane 

Downstream Products

• 100756-32-9 cis-1,3-di-t-butyl-1-hydroxy-2,2,4,4-tetramesitylcyclotetrasilane 
• 100756-33-0 trans-1,3-di-t-butyl-1-hydroxy-2,2,4,4-tetramesitylcyclotetrasilane 
• 100694-05-1 1,4-di-t-butyl-3,3,6,6-tetramesityl-2,5,7-trioxa-1,3,4,6-tetrasilabicyclo<2.2.1>heptane 
• 100694-02-8 1,4-di-t-butyl-3,3,5,5-tetramesityl-2,6-dioxa-1,3,4,5-tetrasilabicyclo<2.1.1>hexane 
• 100694-04-0 cis-1,3-di-t-butyl-1,3-dichloro-2,2,4,4-tetramesitylcyclotetrasilane 
• 100694-03-9 1,3-di-t-butyl-2,2,4,4-tetramesityl-5-oxa-1,2,3,4-tetrasilabicyclo<1.1.1>pentane 
• 100694-01-7 1-t-butyl-2,2-dimesityl-1,1,2-trichlorodisilane 
• 444584-88-7 1-chloro-1-[2-(dimethylaminomethyl)phenyl]-1,2,2-tris(2,4,6-trimethylphenyl)disilane 
• 100694-06-2 1-t-butyl-2,2-dimesityldisilane 

Relevant academic research and scientific papers

SILICIUMVERBINDUNGEN MIT STARKEN INTRAMOLEKULAREN STERISCHEN WECHSELWIRKUNGEN. XVII. SYNTHESE UND KONFORMATION EINES 2,4,6-TRI-t-BUTYLPHENYL-SUBSTITUIERTEN DISILANS

The reaction of trifluoro(2,4,6-tri-t-butylphenyl)silane with dimesithylsilyllithium gives 1,1-difluoro-2,2-dimesityl-1-(2,4,6-tri-t-butylphenyl)disilane which has been characterized by X-ray structure analysis and empirical force field calculations.

TOWARDS TETRASILABICYCLOBUTANE: REDUCTIVE COUPLING OF 1-t-BUTYL-2,2-DIMESITYL-1,1,2-TRICHLORODISILANE

Reductive coupling of 1-t-butyl-2,2-dimesityl-1,1,2-trichlorodisilane employing Li-naphthalenide furnishes, on oxygenation or hydrolysis of the reaction mixture, products (8-11) that may arise from insertion of oxygen into or the addition of water across