4519-17-9

Usage

Uses

Used in Organic Synthesis:
1,4-Bis(vinyldimethylsilyl)benzene is used as an intermediate in organic synthesis for the production of a wide range of chemical compounds. Its reactivity allows for the creation of new molecules with potential applications in various industries.
Used in Silicone Polymers:
1,4-BIS(VINYLDIMETHYLSILYL)BENZENE is used as a precursor in the manufacturing of silicone polymers, which are known for their unique properties such as heat resistance, flexibility, and chemical inertness. These polymers are utilized in a variety of applications, including sealants, adhesives, and coatings.
Used in Chemical Preparations:
1,4-Bis(vinyldimethylsilyl)benzene is employed in the preparation of other chemical products, leveraging its reactivity and the ability to form stable carbon-silicon bonds. This makes it a versatile building block in the chemical industry.
Used in the Production of Specialty Materials:
Due to its unique structure and reactivity, 1,4-bis(vinyldimethylsilyl)benzene is used in the development of specialty materials with tailored properties for specific applications, such as high-performance plastics and advanced composites.

InChI:InChI=1/C14H22Si2/c1-7-15(3,4)13-9-11-14(12-10-13)16(5,6)8-2/h7-12H,1-2H2,3-6H3

Upstream product

• 1719-58-0 Chlorodimethylvinylsilane 
• 17763-88-1 1,4-phenylene bis(trifluoromethanesulfonate) 
• 1078-97-3 1,4-bis(dimethylchlorosilyl)benzene 
• 1826-67-1 vinyl magnesium bromide 
• 106-37-6 1.4-dibromobenzene 

Downstream Products

• 1267749-83-6 1-[(1-heptynyl)dimethylsilyl]-4-(dimethylvinylsilyl)benzene 
• 1267749-75-6 1-{[(triethylsilyl)ethynyl]dimethylsilyl}-4-(dimethylvinylsilyl)benzene 
• 33002-32-3 1,4-Bis-(dimethyl-triethylsilanylethynyl-silanyl)-benzene 
• 1267749-81-4 1-{[(cyclohexyl)ethynyl]dimethylsilyl}-4-(dimethylvinylsilyl)benzene 
• 1267749-76-7 1-{[(dimethylphenylsilyl)ethynyl]dimethylsilyl}-4-(dimethylvinylsilyl)benzene 
• 1267749-77-8 C₂₃H₃₈OSi₃ 
• 1267749-78-9 C₃₂H₅₄O₂Si₄ 
• 1267749-79-0 1-{[3-methyl-3-(trimethylsiloxy)pent-1-ynyl]dimethylsilyl}-4-(dimethylvinylsilyl)benzene 
• 1267749-80-3 C₂₈H₅₀O₂Si₄ 
• 1228307-61-6 1,4-bis{[(E)-2-(1',3',2'-dioxaborinan-2'-yl)ethen-1-yl]dimethylsilyl}benzene 

Relevant academic research and scientific papers

Cross-Electrophile C(sp2)?Si Coupling of Vinyl Chlorosilanes

The cross-electrophile coupling has become a powerful tool for C?C bond formation, but its potential for forging the C?Si bond remains unexplored. Here we report a cross-electrophile Csp2-Si coupling reaction of vinyl/aryl electrophiles with vinyl chlorosilanes. This new protocol offers an approach for facile and precise synthesis of organosilanes with high molecular diversity and complexity from readily available materials. The reaction proceeds under mild and non-basic conditions, demonstrating a high step economy, broad substrate scope, wide functionality tolerance, and easy scalability. The synthetic utility of the method is shown by its efficient accessing of silicon bioisosteres, the design of new BCB-monomers, and studies on the Hiyama cross-coupling of vinylsilane products.

CAPPED DUAL-HEADED ORGANOALUMINUM COMPOSITIONS

The present disclosure relates to a capped dual-headed organoaluminum composition having the formula (I) and processes to prepare the same. In at least one aspect, the capped dual-headed organoaluminum compositions can be used in olefin polymerization.

High temperature thermosets derived from benzocyclobutene-containing main-chain oligomeric carbosilanes

A series of benzocyclobutene-carbosilane thermosets derived from benzocyclobutene-containing oligomeric silylenephenylene (PBSEPs) were synthesized. DSC analysis results demonstrated that the reaction of PBSEPs presumably took place within the temperature