1112-55-6

Basic information

• Product Name: TETRAVINYLSILANE
• Synonyms: (CH2=CH)4Si;Silane, tetravinyl-;tetraethenyl-silan;TETRAVINYLSILANE;TETRAVINYLSILANE 97%;Tetraethenylsilane;Tetravinylsilane,97%;Silane, tetraethenyl-
• CAS NO: 1112-55-6
• Molecular Formula: C₈H₁₂Si
• Molecular Weight: 136.27
• EINECS: 214-192-0
• Product Categories: Others;monomer;Organometallic Reagents;Organosilicon
• Mol File: 1112-55-6.mol
• Article Data: 6

Chemical Properties

• Melting Point: <0°C
• Boiling Point: 130-131 °C(lit.)
• Flash Point: 43 °F
• Appearance: clear yellow liquid
• Density: 0.8 g/mL at 25 °C(lit.)
• Vapor Pressure: 12mmHg at 25°C
• Refractive Index: n20/D 1.461(lit.)
• Water Solubility: 7.26mg/L at 20℃
• BRN: 1739438
• CAS DataBase Reference: TETRAVINYLSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: TETRAVINYLSILANE(1112-55-6)
• EPA Substance Registry System: TETRAVINYLSILANE(1112-55-6)

Safety Data

• Hazard Codes: F,Xi
• Statements: 11-36/37/38
• Safety Statements: 16-26-36/37/39
• RIDADR: UN 1993 3/PG 2
• WGK Germany: 3
• F: 10-21
• TSCA: Yes
• HazardClass: 3.1
• PackingGroup: II
• Hazardous Substances Data: 1112-55-6(Hazardous Substances Data)

Usage

Chemical Properties

clear yellow liquid

Uses

Tetravinylsilane is a useful research chemical compound.

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

Downstream Products

• 18243-27-1 dimethylvinylsilane 
• 18244-95-6 methyltrivinylsilane 
• 1745-72-8 dichlorodivinylsilane 
• 75-94-5 trichlorovinylsilane 
• 1871-21-2 chlorotrivinylsilane 
• 67776-46-9 tetrakis[2-(trichlorosilyl)ethyl]silane 
• 637-69-4 4-Methoxystyrene 
• 827-54-3 2-naphthylethylene 
• 108-57-6 1,3-divinylbenzene 
• 4840-92-0 1-iodo-3-vinylbenzene 
• 1434508-17-4 (E)-1,2-bis(3-vinylphenyl)ethene 
• 105-06-6 1,4-Divinylbenzene 
• 2351-50-0 4-iodostyrene 

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 articles and documents

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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

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)).