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2,2,3,3,3-PENTAFLUOROPROPOXYLMETHYLOXIRANE is a colorless liquid chemical compound with the molecular formula C6H4F5O2, characterized by a slightly sweet odor and high flammability.

706-89-8

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706-89-8 Usage

Uses

Used in Organic Synthesis:
2,2,3,3,3-PENTAFLUOROPROPOXYLMETHYLOXIRANE is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of desired products.
Used in Solvent Applications:
As a solvent, 2,2,3,3,3-PENTAFLUOROPROPOXYLMETHYLOXIRANE is utilized in dissolving and processing certain substances, taking advantage of its solvency properties to enhance reaction rates or improve product quality.
Used in Polymer Production:
2,2,3,3,3-PENTAFLUOROPROPOXYLMETHYLOXIRANE is employed in the production of polymers, where it may act as a monomer or a component in the synthesis of polymeric materials with specific properties.
Used as a Chemical Intermediate:
In the chemical industry, 2,2,3,3,3-PENTAFLUOROPROPOXYLMETHYLOXIRANE serves as an intermediate in the synthesis of more complex molecules, playing a crucial role in the production of various end products.

Check Digit Verification of cas no

The CAS Registry Mumber 706-89-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 706-89:
(5*7)+(4*0)+(3*6)+(2*8)+(1*9)=78
78 % 10 = 8
So 706-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H7F5O2/c7-5(8,6(9,10)11)3-12-1-4-2-13-4/h4H,1-3H2

706-89-8SDS

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 2-(2,2,3,3,3-pentafluoropropoxymethyl)oxirane

1.2 Other means of identification

Product number -
Other names 2,2,3,3,3-PENTAFLUORO-1-PYRIDIN-2-YL-ETHANOL

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:706-89-8 SDS

706-89-8Downstream Products

706-89-8Relevant academic research and scientific papers

An approach to fluorinated surface coatings via photoinitiated cationic cross-linking of mixed epoxy and fluoroepoxy systems

Matuszczak, Stephen,Feast, W. James

, p. 269 - 277 (2000)

The synthesis and characterisation of four polyfluorinated monoepoxides is described. These fluoroepoxy monomers were cationically polymerised either neat or as mixtures with diglycidylether of bisphenol-A using the initiator system (CH3CH2)3Al/H2O (2/1) or the photoinitiator Ph2I+, PF6-. Contact angle measurements indicated that, in favourable cases, the fluorinated epoxide monomer surface segregated at low loadings to give significant lowering of the surface free energy of photocured films of diglycidylether of bisphenol-A.

Sulfated anionics with short perfluoroalkyl chains and preparation method thereof

-

Paragraph 0186-0189, (2017/09/06)

The present invention relates to a fluorinated sulfate anionic surfactant comprising a short fluorinated alkyl group, and a production method thereof. The fluorinated sulfate anionic surfactant comprising a perfluorinated alkyl group according to the present invention has low surface tension despite having a short fluorinated alkyl group, has high solubility for water in a salt state, and has excellent performance, thereby being able to be usefully used as an anionic surfactant.COPYRIGHT KIPO 2017

[(Polyfluoroalkoxy)methyl]thiiranes and 2-anilinoethanethiols

Guseinova,Magerramov,Allakhverdiev

experimental part, p. 946 - 949 (2009/06/18)

By reaction of appropriate oxiranes with thiourea [(polyfluoroalkoxy) methyl]-substituted thiiranes were obtained that are key compounds for the synthesis of perfluoro-containing 1,2-aminopropanethiols.

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