1112-55-6

Usage

Uses

Used in Chemical Research:
Tetravinylsilane is used as a research chemical compound for various applications in the field of chemistry. Its unique properties allow it to be used in the synthesis of new materials and compounds, as well as in the study of silicon-based chemistry.
Used in Silicon-based Chemistry:
Tetravinylsilane is used as a precursor in the synthesis of various silicon-containing materials and compounds. Its reactivity and versatility make it a valuable building block for the development of new materials with potential applications in various industries.
Used in Material Science:
Tetravinylsilane is used as a component in the development of new materials with unique properties. Its ability to form stable bonds with other elements allows it to be incorporated into a wide range of materials, including polymers, ceramics, and composites.
Used in Nanotechnology:
Tetravinylsilane is used in the field of nanotechnology for the synthesis of nanomaterials and the development of new nanostructures. Its ability to form stable bonds with other elements makes it a promising candidate for the creation of novel nanomaterials with potential applications in various fields, such as electronics, medicine, and energy.
Used in Electronics Industry:
Tetravinylsilane is used in the electronics industry for the development of new materials with improved electrical and thermal properties. Its incorporation into semiconductor materials and other electronic components can lead to enhanced performance and reliability.
Used in Pharmaceutical Industry:
Tetravinylsilane is used in the pharmaceutical industry for the synthesis of new drug candidates and the development of drug delivery systems. Its unique chemical properties make it a valuable tool in the design and synthesis of novel pharmaceutical compounds with potential therapeutic applications.
Used in Environmental Applications:
Tetravinylsilane is used in environmental applications for the development of materials with potential use in pollution control and remediation. Its ability to form stable bonds with other elements allows it to be incorporated into materials that can be used to remove contaminants from air, water, and soil.

Flammability and Explosibility

Flammable

InChI:InChI=1/C8H12Si/c1-5-9(6-2,7-3)8-4/h5-8H,1-4H2

Upstream product

• 75-01-4 chloroethylene 
• 3536-96-7 vinylmagnesium chloride 
• 1826-67-1 vinyl magnesium bromide 
• 2372-31-8 triethenylsilane 
• 75-94-5 trichlorovinylsilane 
• 74045-42-4 1,1-Divinyl-1-silacyclobutane 

Downstream Products

• 67776-46-9 tetrakis[2-(trichlorosilyl)ethyl]silane 
• 1871-21-2 chlorotrivinylsilane 
• 110-56-5 1,4-dichlorobutane 
• 18825-61-1 tetrakis(2-diphenylphosphinoethyl)silane 
• 86811-75-8 (π-tetravinylsilane)bis(triphenylphosphine)dinickel 
• 86811-74-7 (π-tetravinylsilane)triphenylphosphinenickel 
• 1436412-60-0 1,3-diisopropyl-2-(4-vinylphenyl)guanidine 
• 1436412-61-1 1,3-diisopropyl-2-(3-vinylphenyl)guanidine 
• 1436412-62-2 2-(2-fluoro-4-vinylphenyl)-1,3-diisopropylguanidine 
• 1436412-63-3 2-(2,5-dimethyl-4-vinylphenyl)-1,3-diisopropylguanidine 
• 637-69-4 4-Methoxystyrene 

Related news

Coordination environment friendly silicon in copper(I) chloride π-complexes with TETRAVINYLSILANE (cas 1112-55-6) and dimethyltetravinyldisiloxane08/20/2019

Two crystal complexes of copper(I) chloride with tetravinylsilane (TVS) dimethyltetravinyldisiloxane (DMTVDS) were prepared and examined by IR spectroscopy and X-ray diffraction: sp. gr. P2/a, Z = 4, a = 13.428(1) Å, b = 7.9584(7) Å, c = 14.694(1) Å for [Cu4Cl4(TVS)]; sp. gr. P21/c, a = 10.505(1...detailed

Dissociative electron attachment to the silane derivatives trichlorovinylsilane (SiCl3C2H3), TETRAVINYLSILANE (cas 1112-55-6) (Si(C2H3)4) and trimethylvinylsilane (Si(CH3)3C2H3)08/19/2019

The formation of negative ions following low energy (0–12 eV) electron attachment to the title compounds is studied in a crossed electron-molecular beam experiment applying mass spectrometric detection of the anions. All silane derivatives presently studied are weak electron scavengers which al...detailed

Depth profile of mechanical properties of plasma-polymerized TETRAVINYLSILANE (cas 1112-55-6) films evaluated by cyclic nanoindentation08/17/2019

Plasma-polymerized tetravinylsilane films deposited on silicon wafers by PECVD at different powers using pulsed plasma were analyzed by both typical conventional depth sensing and by cyclic nanoindentation. A comparative study of the two methods was carried out under reduced system drift. It was...detailed

Enhanced interfacial adhesion of glass fibers by TETRAVINYLSILANE (cas 1112-55-6) plasma modification08/15/2019

Plasma-polymerized tetravinylsilane was used to surface modify glass fibers to improve interfacial adhesion of a GF/polyester composite. Plasma polymer films of controllable thickness and physicochemical properties were deposited on unsized glass fibers by RF pulsed plasma using an effective pow...detailed

Plasma polymer films of TETRAVINYLSILANE (cas 1112-55-6) modified by UV irradiation08/14/2019

As-deposited plasma polymer films of tetravinylsilane were modified by UV irradiation at ambient conditions. Surface and bulk spectroscopic techniques confirmed significant changes in chemical composition and structure that resulted in increased mechanical constants (Young's modulus, hardne...detailed

Relevant academic research and scientific papers

Method for synthesizing tetravinyl silane

The invention discloses a method for synthesizing tetravinyl silane, which comprises the following steps of: one. The mixed organic solvent comprises first organic solvent and second organic solvent, first organic solvent is tetrahydrofuran, second organic solvent is an organic solvent immiscible with water. The reaction temperature is controlled to 30 °C - 35 °C by dropwise adding vinyl magnesium chloride dropwise. After completion of the reaction, the reaction is quenched with a weak acidic aqueous solution. After the quenching reaction is complete, the organic layer is directly rectified to obtain the product. The method has the advantages that the operation steps are simple, the reaction steps are few, the purification is easy, and the purity of the obtained tetravinyl silane is high.

METHOD FOR PRODUCING TETRAALKENYLSILANE

PROBLEM TO BE SOLVED: To provide an efficient method for producing a tetraalkenylsilane with improved production efficiency per unit volume of a reactor. SOLUTION: Provided is a method for producing a tetraalkenylsilane represented by general formula (3), comprising reacting an alkenyl trihalosilane represented by general formula (1) (in the formula, X represents a halogen atom and n represents an integer of 0 to 16. The same holds for general formulas (2) and (3)) with a Grignard compound represented by general formula (2). SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Side products in the syntheses of vinylsilanes and vinylsiloxanes using vinylmagnesium chloride

Impurity of moisture in the solvent (tetrahydrofuran) alters the, normal scheme of formation of vinylmagnesiumm chloride and gives rise to several unexpected products: benzene, toluene, and methyl chloride. Side products forming in alkali hydrolysis of trivinylsilane and hydrochlorination of tetravinylsilane were isolated and identified.

Silaethenes, XV. Pyrolysis of 1-Methyl-1-vinyl-1-silacyclobutane and 1,1-Divinyl-1-silacyclobutane - Follow-up Reactions of the Silaethenes Me(Vi)Si=CH2 and Vi2Si=CH2

The pyrolysis of the silacyclobutanes Vi(Me)Si(CH2)3 (VMS) and Vi2Si(CH2)3 (V2S) at 700-800 deg C and 1E-1 - 1E-2 mbar leads to the intermediates Vi(Me)Si=CH2 and Vi2Si=CH2, which undergo isomerisation to siliranes followed by cleavage to give allene and the corresponding silylenes Me(H)Si: and Vi(H)Si: respectively.Copyrolyes of these silacyclobutanes with dienes (2,3-dimethyl-1,3-butadiene or isoprene) yield silacyclopentene derivatives (4, 14 and 20).The formation of these products supports the proposed mechanism.The simultaneous existence of silaethenes and silylenes in the gas phase is proven by the presence of the disilacyclobutanes 13 and 17, respectively, in the reaction mixtures.Using isoprene as the quenching reagent for Vi(Me)Si=CH2 the two isomeric silacyclohexenes 15 and 16 are formed in low yield, in addition to almost equal amounts of 13 and 14 (eq. (6)).