1112-55-6 | Tetravinylsilane

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$74.00	$52.00
5g	97%	in stock	$251.00	$176.00

Description

• Catalog Number: AB50429
• Chemical Name: Tetravinylsilane
• CAS Number: 1112-55-6
• Molecular Formula: C8H12Si
• Molecular Weight: 136.2664
• MDL Number: MFCD00008607
• SMILES: C=C[Si](C=C)(C=C)C=C
• NSC Number: 113262

Computed Properties

• Complexity: 107
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Rotatable Bond Count: 4

Upstream Synthesis Route

Tetravinylsilane is a versatile organosilicon compound that finds wide application in chemical synthesis. Its unique properties make it a valuable reagent in various reactions. In organic synthesis, Tetravinylsilane is commonly used as a dienophile in Diels-Alder reactions, where it reacts with dienes to form cyclohexenes. This reaction is utilized in the construction of complex organic molecules with multiple stereocenters.Additionally, Tetravinylsilane is often employed in transition metal-catalyzed cross-coupling reactions to introduce vinyl groups into organic molecules. This strategy allows for the creation of diverse carbon-carbon bonds, enabling the synthesis of various functionalized compounds. The presence of vinyl groups in the Tetravinylsilane molecule offers a convenient handle for further functionalization, facilitating the generation of complex molecular architectures.Furthermore, Tetravinylsilane serves as a precursor for the synthesis of various silicon-containing materials. Through hydrosilylation reactions, Tetravinylsilane can be used to introduce vinyl groups onto silicon-based surfaces or polymers, enhancing their chemical reactivity and allowing for the development of advanced materials with tailored properties.Overall, the diverse applications of Tetravinylsilane in chemical synthesis highlight its significance as a valuable building block for the creation of intricate organic molecules and functional materials.

Literature

• Ionic chemistry of tetravinylsilane cation (TVS+) formed by electron impact: theory and experiment.

  The journal of physical chemistry. A 20090611

• Approaches to the preparation of carborane-containing carbosilane compounds.

  Organic letters 20050120