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Oxirane, 2-fluoro-2-(pentafluoroethyl)-3,3-bis(trifluoromethyl)-, also known as 2-fluoro-2-(pentafluoroethyl)-3,3-bis(trifluoromethyl)oxirane, is a halogenated organic compound with the chemical formula C5F10O. It is a colorless liquid at room temperature and is characterized by its highly fluorinated structure, which contributes to its unique chemical and physical properties. Oxirane, 2-fluoro-2-(pentafluoroethyl)-3,3-bis(trifluoromethyl)- is primarily used in the synthesis of various fluoropolymers and as an intermediate in the production of pharmaceuticals and agrochemicals. Due to its stability and reactivity, it is also employed as a building block in the development of new materials with specific properties, such as improved thermal and chemical resistance.

788-67-0

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788-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 788-67-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 788-67:
(5*7)+(4*8)+(3*8)+(2*6)+(1*7)=110
110 % 10 = 0
So 788-67-0 is a valid CAS Registry Number.

788-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-2-(1,1,2,2,2-pentafluoroethyl)-3,3-bis(trifluoromethyl)oxirane

1.2 Other means of identification

Product number -
Other names 2,3-epoxyperfluoro-2-methylpentane

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:788-67-0 SDS

788-67-0Relevant academic research and scientific papers

FLUOROALIPHATIC ESTERS OF FLUOROSULFONIC ACID. 2. REACTION BIS(FLUOROSULFATO)PERFLUOROALKANES WITH CESIUM FLUORIDE

Rogovik, V. M.,Delyagina, N. I.,Mysov, E. I.,Cherstkov, V. F.,Sterlin, S. R.,German, L. S.

, p. 1870 - 1876 (2007/10/02)

2,3-Bis(fluorosulfato)perfluoroalkanes split under the action of CsF in the absence of solvents, giving a mixture of α-fluorosulfatoperfluoro ketones, perfluoroalkene sulfates, and perfluoro α-diketones.The occurence of these reactions in solutions results mainly in the formation of oxides of the corresponding fluoroolefins or products of their conversions.The reactions carried out are the first examples of nucleophilic substitution at a secondary carbon atom in a perfluorinated saturated chain.

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