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460-43-5

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460-43-5 Usage

General Description

2,2,2-Trifluoroethyl Methyl Ether is a chemical compound known for its unique properties. Its molecular formula is C3H5F3O, which denotes the presence of hydrogen, carbon, fluorine, and oxygen. It is composed of an ether functional group, meaning it includes a pair of carbon atoms linked by an oxygen atom. An important element in the composition is the three fluorine atoms attached to a carbon, which give it its trifluoroethyl group, contributing to its overall stability, and reactivity. 2,2,2-TRIFLUOROETHYL METHYL ETHER can be used in various chemical reactions due to these properties, but safety measures should be taken to handle it due to unknown hazards it may pose upon exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 460-43-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 460-43:
(5*4)+(4*6)+(3*0)+(2*4)+(1*3)=55
55 % 10 = 5
So 460-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H5F3O/c1-7-2-3(4,5)6/h2H2,1H3

460-43-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L17887)  2,2,2-Trifluoroethyl methyl ether, 99+%   

  • 460-43-5

  • 5g

  • 419.0CNY

  • Detail
  • Alfa Aesar

  • (L17887)  2,2,2-Trifluoroethyl methyl ether, 99+%   

  • 460-43-5

  • 25g

  • 1049.0CNY

  • Detail

460-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-TRIFLUOROETHYL METHYL ETHER

1.2 Other means of identification

Product number -
Other names 1,1,1-trifluoro-2-methoxyethane

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:460-43-5 SDS

460-43-5Relevant articles and documents

Solvolysis in 2,2,2-Trifluoroethanol-Water and 2,2,2-Trifluoroethanol-Etanol Mixtures. Selectivity of the Intermediates and N Values

Kaspi, Joseph,Rappoport, Zvi

, p. 3829 - 3837 (1980)

Solvolysis of 1-adamantyl bromide (1-Br) in eight TFE-EtOH mixtures gave a Grunwald-Winstein mGW value of 1.50, and the ethyl (1-OEt) and trifluoroethyl (1-OTFE) ethers.The selectivity ratios for reaction with the solvent components kTFE/kEtOH are medium dependent, being 2.60-0.83.In TFE-H2O, mGW = 0.56 and the kTFE/KH2O ratios increase with ΧH2O from 0.49 to 2.04.Solvolysis of 1-anisyl-2-methylpropen-1-yl tosylate (2-OTs) in TFE-EtOH gives mGW = 0.89 and an average kTFE/kEtOH value of 0.086.Methyl tosylate was solvolyzed in several TFE-EtOH and TFE- H2O mixtures and new values of the nucleophilic parameter N were determined.Products were derived from the free cation in the solvolysis of 2-OTs and from the solvent-separated ion pair in the solvolysis of 1-Br, and the selectivities of these species were analyzed.The nucleophilicities of TFE-H2O and TFE-EtOH mixtures and the recent use of the comparison od TFE-H2O and EtOH-H2O mixtures for evaluating solvent participation in solvolysis reactions were discussed.

Preparation of Methyl Fluoroalkyl Ethers

-

Page/Page column 4, (2010/12/29)

Methyl fluoroalkyl ether can be produced by the reaction of a fluoroalkyl alcohol with chloromethane. The process involves reacting an alkoxide of a fluoroalkyl alcohol with chloromethane.

Methyl hypofluorite (MeOF) reactions with various fluoroolefins

Suzuta, Tetsuya,Abe, Takashi,Sekiya, Akira

, p. 3 - 8 (2007/10/03)

The reaction of methyl hypofluorite (MeOF) with certain fluoroolefins, such as CF2=CF2, CF2=CFCF3, CF2=CFOCF3, CF2=CFOMe, CF2=CClF, CF2=CHF, CF2=CH2, CHF=CH2, CF2=CFCF=CF2, occurred in CD3CN or in the presence of NaF. Using neat MeOF in the presence of NaF was a novel method and gave good results. We observed that when more than three fluorine atoms are bonded to the C-C double bond, the addition products were obtained in mostly good yields.

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