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359-72-8

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359-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359-72-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 359-72:
(5*3)+(4*5)+(3*9)+(2*7)+(1*2)=78
78 % 10 = 8
So 359-72-8 is a valid CAS Registry Number.

359-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name perfluoro-2-methyl-2-pentene

1.2 Other means of identification

Product number -
Other names 1,1,3,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)-1-pentene

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:359-72-8 SDS

359-72-8Relevant articles and documents

Development of technology of perfluoroethyl isopropyl ketone production

Fenichev,Babenko,Bispen,Moldavskii

, p. 376 - 386 (2013/07/05)

Synthesis of perfluoroethyl isopropyl ketone by an interaction of hexafluoropropene with perfluoropropionic acid fluoride or hexafluoropropene oxide was examined. Interchangeability of perfluoropropionic acid fluoride and hexafluoropropene oxide was demonstrated. The features of perfluoroethyl isopropyl ketone synthesis were studied in polar aprotic solvents on catalysts: alkali metal fluoride. A method for obtaining perfluoroethyl isopropyl ketone by direct catalytic reaction in a tubular reactor without use of solvents was suggested and investigated. The mechanism of interaction was considered. The main impurities resulting in obtaining perfluoroethyl isopropyl ketone were determined. The methods of cleaning perfluoroethyl isopropyl ketone were worked out.

REACTION OF 2-TRIFLUOROMETHYLPERFLUORO-2-PENTENYL FLUOROSULFATE WITH NUCLEOPHILIC REAGENTS

Avetisyan, E. A.,Cherstkov, V. F.,Snegirev, V. F.,Sterlin, S. R.,German, L. S.

, p. 615 - 618 (2007/10/02)

2-Trifluoromethylperfluoro-2-pentenyl fluorosulfate undergoes SN2' nucleophilic reactions.The reaction of this fluorosulfate with halide salts gives an equilibrium mixture of 1-halo-2-trifluoromethylperfluoro-2-pentene and 2-trifluoromethyl-3-haloperfluoro-1-pentene.

ALKYLATION OF PERFLUORO-2-METHYL-2-PENTYLCARBANION WITH ALKYL AND ALLYL HALIDES

Dmowski, Wojciech,Wozniacki, Ryszard

, p. 385 - 394 (2007/10/02)

Perfluoro-2-methyl-2-pentylcarbanion, generated from perfluoro-4-methyl-2-pentene in an aprotic solvent, reacted with halides RX, where R = alkyl or allyl and X = I, Br, or Cl, to give fluorohydrocarbons of the general formula CF3CF2CF2C(CF3)2R.No reaction with iso-propyl iodide and with 1-iodo-2,2,2-trifluoroethane occured.The reaction with 1-iodo-3,3,3-trifluoropropane resulted in the formation of 3,3,3-trifluoropropene and 2-H-perfluoro-2-methylpentane.

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