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Silane, 1,2-ethenediylbis[trichloro-], also known as 1,2-bis(trichlorosilyl)ethane or Si2Cl6C2H2, is a chemical compound that consists of a silicon-carbon backbone with two trichlorosilyl groups attached to the carbon atoms. This organosilicon compound is used as a coupling agent in the production of composite materials, particularly in the reinforcement of glass fibers with resins. It enhances the adhesion between the inorganic glass fibers and the organic polymer matrix, resulting in improved mechanical properties and durability of the composite material. The compound is also utilized in the synthesis of other organosilicon compounds and as a precursor in the production of silicones. Due to its reactivity and potential hazards, it is important to handle Silane, 1,2-ethenediylbis[trichloro- with care, following appropriate safety measures.

692-52-4

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692-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 692-52-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 692-52:
(5*6)+(4*9)+(3*2)+(2*5)+(1*2)=84
84 % 10 = 4
So 692-52-4 is a valid CAS Registry Number.

692-52-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name trichloro(2-trichlorosilylethenyl)silane

1.2 Other means of identification

Product number -
Other names 1,2-Bis-trichlorsilyl-ethylen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:692-52-4 SDS

692-52-4Relevant academic research and scientific papers

Reaction of Hexachlorodisilane with Trichloroethynylsilane and 2-Propynyl Chloride in the Gas Phase

Chernyshev,Komalenkova,Kapitova,Bykovchenko,Khromykh,Bochkarev

, p. 1043 - 1046 (2007/10/03)

Reaction of acetylenic compounds (trichloroethynylsilane and 2-propynyl chloride) with hexachlorodisilane in the gas phase at 450-520°C was studied. Main products of the reaction were identified, and a mechanism of their formation was proposed. It was shown that of the two reaction centers of 2-propynyl chloride (C=≡C and C-Cl) only the C-Cl bond is involved in reaction with dichlorosilylenes generated from hexachlorodisilane.

Gas-Phase Reactions of Hexachlorodisilane with Vinyl Chloride and Allyl Chloride

Chernyshev,Komalenkova,Kapitova,Bykovchenko,Khromykh,Bochkarev

, p. 1447 - 1450 (2007/10/03)

Gas-phase reactions of hexachlorodisilane with vinyl chloride and allyl chloride is studied. Dichlorosilylene generated from Si2Cl6 reacts with the above chloroalkenes mainly at the C-Cl bond to form alkenyltrichlorosilanes. The yields of vinyltrichlorosilane and allyltrichlorosilane are 45-63 and 49-81%, respectively. A mechanism of the reactions of Si2Cl6 with vinyl chloride and allyl chloride is proposed.

Gas-phase reactions of hexachlorodisilane with chloroform, carbon tetrachloride, and Di- and tetrachloroethylenes

Chernyshev,Komalenkova,Kapitova,Bykovchenko

, p. 1113 - 1116 (2007/10/03)

Gas-phase reactions of hexachlorodisilane with chloroalkanes (CHCl3 and CCl4) and chloroalkenes (ClCH=CHCl and Cl2C=CCl2) are studied. Dichlorosilylenes generated from Si2Cl6 insert into the C-Cl bonds in chloroalkanes; with chloroalkenes, insertion into the C-Cl bonds occurs along with cyclo-addition to the C=C bonds.

PALLADIUM COMPLEXES IN THE HYDROSILYLATION OF ACETYLENE

Kopylova, L. I.,Pukhnarevich, V. B.,Voronkov, M. G.

, p. 276 - 278 (2007/10/02)

The catalytic activities of triphenylphosphine-, trialkylphosphine-, and acetylacetone-palladium complexes in the hydrosilylation of acetylene with trichloro-, alkyldichloro-, triethyl, and triethoxy-silanes were investigated.The yields of the corresponding (triorganylsilyl)ethylenes and 1,2-bis(triorganylsilyl)ethanes (conditions: 70-80 deg C, solvent xylene) depend on the nature of the ligands on the palladium atom and the character of the substituents on the silicon atom in the hydride silane.

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