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3,3,4,4,5,5,6,6,6-nonafluorohexanoyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64018-24-2

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64018-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64018-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,1 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64018-24:
(7*6)+(6*4)+(5*0)+(4*1)+(3*8)+(2*2)+(1*4)=102
102 % 10 = 2
So 64018-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H2ClF9O/c7-2(17)1-3(8,9)4(10,11)5(12,13)6(14,15)16/h1H2

64018-24-2SDS

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 3,3,4,4,5,5,6,6,6-nonafluorohexanoyl chloride

1.2 Other means of identification

Product number -
Other names Hexanoyl chloride,3,3,4,4,5,5,6,6,6-nonafluoro

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:64018-24-2 SDS

64018-24-2Downstream Products

64018-24-2Relevant academic research and scientific papers

Light-fluorous TEMPO: reagent, spin trap and stable free radical

Dobbs, Adrian P.,Jones, Peter,Penny, Mark J.,Rigby, Stephen E.

supporting information; experimental part, p. 5271 - 5277 (2009/11/30)

The synthesis of two light-fluorous TEMPO derivatives is reported, along with their fluorous-organic solvent partition coefficients and their ESR spectra. Applications of the fluorous-TEMPO reagents in oxidation reactions and as radical traps are discussed.

Novel light-fluorous TEMPO reagents and their application in oxidation reactions

Dobbs, Adrian P.,Penny, Mark J.,Jones, Peter

scheme or table, p. 6955 - 6958 (2009/04/07)

The synthesis of two light-fluorous TEMPO derivatives is reported, along with their application in oxidation reactions.

Synthesis of 2H,2H-perfluoroalkyl and 2H-perfluoroalkenyl carboxylic acids and amides

Achilefu, Samuel,Mansuy, Laurence,Selve, Claude,Thiebaut, Sylvie

, p. 19 - 26 (2007/10/02)

An efficient and convenient procedure for the synthesis of 2-perfluoroalkyl ethanoic acids by direct oxidation of 2-perfluoroalkyl ethanols with Jones' reagent (CrO3/H2SO4) is described.Treatment of the acids with aqueous sodium hydroxide gave 3-perfluoroalkyl, 3-fluoro-2,3-propenyl carboxylic acids wich may be used for the preparation of the corresponding chlorides and amides. - Keywords: Synthesis; 2-Perfluoroalkyl ethanoic acids; Jones' reagent; NMR spectroscopy; IR spectroscopy

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