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2441-27-2

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2441-27-2 Usage

General Description

Trichloro(1-chlorovinyl)silane is a chemical compound with the molecular formula C2HCl4Si. It is a clear, colorless to slightly yellow liquid with a pungent odor, commonly used in the production of silicone polymers and other silicone-based products. Trichloro(1-chlorovinyl)silane is highly reactive and flammable, requiring careful handling and storage. It is also toxic if inhaled or absorbed through the skin, and can cause irritation to the eyes, skin, and respiratory system. Due to its hazardous nature, trichloro(1-chlorovinyl)silane should only be used by trained professionals in a well-ventilated area and with appropriate protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 2441-27-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2441-27:
(6*2)+(5*4)+(4*4)+(3*1)+(2*2)+(1*7)=62
62 % 10 = 2
So 2441-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H2Cl4Si/c1-2(3)7(4,5)6/h1H2

2441-27-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trichloro(1-chloroethenyl)silane

1.2 Other means of identification

Product number -
Other names EINECS 219-473-1

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:2441-27-2 SDS

2441-27-2Relevant articles and documents

Polyfluoroalkyl derivatives of silicon. Part XIII. Preparation and pyrolysis of trifluoro(halogenovinyl)silanes and (1-fluoro-2-halogenoethyl)trihalogenosilanes

Haszeldine, Robert N.,Pool, Colin R.,Tipping, Anthony E.

, p. 2177 - 2181 (2007/10/12)

Treatment of 1-chloro-2-fluoroethyl- or 1,2-dichloroethyl-trichlorosilane with quinoline gives trichloro(1-chlorovinyl)silane; trichloro(1,2-dibromoethyl)silane dehydrohalogenates similarly. In contrast 2-chloro-1-fluoro-ethyl- and 1,2-difluoroethyl-trichlorosilane give vinyl fluoride under comparable conditions. Both 1-chlorovinyl-and 1-bromovinyl-trifluorosilane, prepared from the trichlorosilyl analogues, decompose slowly at 280°C to afford acetylene and tetrahalogenosilanes via the suspected intermediacy of the alkylidenecarbene CH2:C:. Pyrolysis of (2-chloro-1-fluoroethyl)trifluorosilane gives vinyl chloride via a carbene intermediate, but the trichlorosilyl analogue yields the rearrangement compound dichloro(1,2-dichloroethyl)fluorosilane. 1,2-Difluoroethyl-trifluorosilane and -trichlorosilane both decompose via a non-carbene mechanism involving β elimination.

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