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667-49-2

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667-49-2 Usage

Safety Profile

Reaction with sodium azide formsa highly explosive solid. When heated to decomposition itemits toxic fumes of F??.

Check Digit Verification of cas no

The CAS Registry Mumber 667-49-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 667-49:
(5*6)+(4*6)+(3*7)+(2*4)+(1*9)=92
92 % 10 = 2
So 667-49-2 is a valid CAS Registry Number.
InChI:InChI=1/C3F4O/c4-1(2(5)6)3(7)8

667-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,3-trifluoroprop-2-enoyl fluoride

1.2 Other means of identification

Product number -
Other names 2,3,3-Trifluor-acrylsaeure-fluorid

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:667-49-2 SDS

667-49-2Relevant articles and documents

ELECTROPHILIC ALKENYLATION OF FLUOROOLEFINS BY PERFLUORO(2-ALKOXYPROPENES)

Chepik, S. D.,Belen'kii, G. G.,German, L. S.

, p. 1712 - 1714 (1991)

Perfluoro(2-alkoxypropenes) react with tetrafluoroethylene under mild conditions in the presence of SbF5 to give the corresponding perfluoro(2-alkoxy-2-pentenes). 1-Trifluoromethoxyperfluoropropene is converted by the action of SbF5 in SO2ClF solution to the acid fluoride derivative of perfluoroacrylic acid.

Novel synthetic route to perfluoroallyl cyanide (PFACN) reacting perfluoroallyl fluorosulfonate with cyanide

Tverdomed, Sergey N.,Hirschberg, Markus E.,Pajkert, Romana,Hintzer, Klaus,R?schenthaler, Gerd-Volker

, p. 65 - 69 (2018/03/21)

A novel synthetic method for the preparation of perfluoroallyl cyanide CF2[dbnd]CFCF2CN (PFACN) is presented. This includes the addition – elimination reaction of cyanide anion with perfluoroallyl fluorosulfate CF2[dbnd]CF

EINSTUFIGE HERSTELLUNG HALOGENIERTER CARBONSAUREFLUORIDE AUS DEN FREIEN SAUREN

Schwertfeger, W.,Siegemund, G.

, p. 237 - 246 (2007/10/02)

The reaction of per- or polyhalogenated carboxylic acids with trifluoromethyl or difluorochloromethyl substituted aromatics takes place in the presence of Lewis-acid-catalysts and forms the corresponding acid fluorides in good to very good yields.

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