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2643-25-6

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2643-25-6 Usage

General Description

1,2,2-Trifluorovinyl-triphenylsilane is a chemical compound with the molecular formula C20H15F3Si. It is a colorless liquid with a melting point of -14°C and a boiling point of 103-104°C. 1,2,2-Trifluorovinyl-triphenylsilane is used as a reagent in organic synthesis and as a building block in the production of various pharmaceutical and agrochemical products. It is also used as a precursor for functional materials and in semiconductor industry. 1,2,2-Trifluorovinyl-triphenylsilane is a highly reactive compound and should be handled with caution in a well-ventilated environment and with proper protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 2643-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2643-25:
(6*2)+(5*6)+(4*4)+(3*3)+(2*2)+(1*5)=76
76 % 10 = 6
So 2643-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H15F3Si/c21-19(22)20(23)24(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

2643-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(1,2,2-trifluoroethenyl)silane

1.2 Other means of identification

Product number -
Other names 1,2,2-trifluorovinyl-triphenylsilane

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:2643-25-6 SDS

2643-25-6Downstream Products

2643-25-6Relevant articles and documents

Fluorinated Vinylsilanes from the Copper-Catalyzed Defluorosilylation of Fluoroalkene Feedstocks

Sakaguchi, Hironobu,Ohashi, Masato,Ogoshi, Sensuke

supporting information, p. 328 - 332 (2017/12/13)

Herein, a copper-catalyzed C?F bond defluorosilylation reaction of tetrafluoroethylene and other polyfluoroalkenes is described. Mechanistic studies, based on a series of stoichiometric reactions with copper complexes, revealed that the key steps of this defluorosilylation reaction are 1) the 1,2-addition of a silylcopper intermediate to the polyfluoroalkene and 2) a subsequent selective β-fluorine elimination, which generates a Cu?F species. The β-fluorine elimination is facilitated by Lewis acidic F?Bpin, which is generated in situ during the defluorosilylation.

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