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58705-93-4

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58705-93-4 Usage

Physical state

Clear, colorless liquid

Odor

Faint ether-like

Usage

Solvent, component in refrigerants and heat transfer fluids

Environmental benefits

Low toxicity, non-flammability, low global warming potential

Chemical structure

Stable and non-reactive with many substances

Boiling point

31.6°C

Suitability

Wide range of applications due to low boiling point

Check Digit Verification of cas no

The CAS Registry Mumber 58705-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,0 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58705-93:
(7*5)+(6*8)+(5*7)+(4*0)+(3*5)+(2*9)+(1*3)=154
154 % 10 = 4
So 58705-93-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H6F6O/c1-12-2-4(7,8)3(6)5(9,10)11/h3H,2H2,1H3

58705-93-4SDS

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 1,1,1,2,3,3-hexafluoro-4-methoxybutane

1.2 Other means of identification

Product number -
Other names 2,2,3,4,4,4-hexafluorobutyl methyl ether

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:58705-93-4 SDS

58705-93-4Relevant articles and documents

Free Radical Chemistry. Part 3. Substituent Effects in Additions of Ethers to Fluorinated Alkenes

Chambers, Richard D.,Grievson, Brian,Kelly, Noel M.

, p. 2209 - 2214 (2007/10/02)

Systematic studies on free-radical addition of acyclic ethers to hexafluoropropene reveal the influence of steric effects on the competitive formation of mono-, di-, and tri-adducts.It is concluded that 'captodative' effects are not dominant in systems containing polyfluoroalkyl groups.Remarkably efficient free-radical additions of trialkyl borates, to fluorinated alkenes occur, but in a series X-OMe (X=MeCO, HCO, MeOCO etc.) reactivity is reduced by electron withdrawal.

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