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80793-21-1

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80793-21-1 Usage

Physical State

Clear, colorless liquid.

Solubility

Insoluble in water.

Stability

Highly stable and non-reactive.

Common Uses

a. Solvent in industrial applications.
b. Surfactant in the production of fluoropolymer coatings.
c. Solvent in cleaning and degreasing processes.
d. Chemical intermediate in the synthesis of other fluorinated compounds.

Industrial Applications

Electronics, automotive, aerospace, and textiles.

Hazardous Nature

Considered hazardous, may pose health and environmental risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 80793-21-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80793-21:
(7*8)+(6*0)+(5*7)+(4*9)+(3*3)+(2*2)+(1*1)=141
141 % 10 = 1
So 80793-21-1 is a valid CAS Registry Number.

80793-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H,1H,1H-PERFLUOROOCTAN-2-ONE

1.2 Other means of identification

Product number -
Other names METHYL PERFLUORO-N-HEXYL KETONE

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:80793-21-1 SDS

80793-21-1Relevant articles and documents

Transition metal complexes bearing NHC ligands substituted with secondary polyfluoroalkyl groups

Kola?íková,?im?nek,Rybá?ková,Cva?ka,B?ezinová,Kví?ala

, p. 19663 - 19673 (2015/11/27)

Using three different approaches, racemic 1-(perfluoroalkyl)ethylamines were synthesized from perfluoroalkyl iodides or perfluoroalkanoic acids, and further transformed to the corresponding N,N′-disubstituted ethane-1,2-diimines and ethane-1,2-diamines as mixtures of diastereoisomers. Their cyclization afforded imidazolium or dihydroimidazolium salts, which led to silver or palladium complexes bearing NHC ligands substituted with secondary polyfluoroalkyl groups. The palladium complexes bearing a throwaway 3-chloropyridine ligand proved to be moderately active in the model Suzuki-Miyaura coupling.

Reactivity of perfluorohexyl iodide with N,N-disubstituted amides and esters in the presence of a metal couple and radical initiator

Benefice-Malouet, S.,Commeyras, A.

, p. 103 - 108 (2007/10/02)

The reactivity of perfluorohexyl iodide with N,N-disubstituted amides or ethyl formate as solvents and reactants, in the presence of a zinc-copper metal couple and radical initiator, has been investigated.In each case, the corresponding perfluorinated carbonyl compounds, such as aldehydes, amides, ketones and esters, were obtained in good yield, thus proving the efficacy of this reaction.The influence of the radical initiator on the reaction mechanisms has been studied and is discussed. - Keywords: Reactivity; Perfluorohexyl iodide; Disubstituted amines; Zinc-copper metal couple; Radical initiator; NMR spectroscopy; IR spectroscopy; Mass spectrometry

REACTION OF METHYLMAGNESIUM IODIDE WITH PERFLUOROCARBOXYLATE ESTERS

Batizat, D. V.,Yarosh, A. A.,Ignatenko, A. V.,Ponomarenko, V. A.

, p. 1022 - 1024 (2007/10/02)

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