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79-53-8

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79-53-8 Usage

Uses

Chloropentafluoroacetone is used to modify other compounds by the addiction of CF3 and CF2Cl groups.

Check Digit Verification of cas no

The CAS Registry Mumber 79-53-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79-53:
(4*7)+(3*9)+(2*5)+(1*3)=68
68 % 10 = 8
So 79-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C3ClF5O/c4-2(5,6)1(10)3(7,8)9

79-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name CHLOROPENTAFLUOROACETONE

1.2 Other means of identification

Product number -
Other names chloropentafluoro-2-propanone

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:79-53-8 SDS

79-53-8Relevant articles and documents

3-CHLOROPENTAFLUOROPROPENE-1,2-OXIDE: PREPARATION AND REACTIONS WITH SOME HETEROATOM NUCLEOPHILES AND ANTIMONY PENTAFLUORIDE

Kvicala, J.,Paleta, O.

, p. 6721 - 6724 (1994)

Nucleophilic epoxidation of 3-chloropentafluoro-1-propene at PTC conditions afforded 3-chloropentafluoropropene-1,2-oxide, which was reacted with some oxygen and nitrogen nucleophiles to 3-chloro-3,3-difluoropropionic acid derivatives.With antimony pentafluoride, mixture of fluorinated acetones was obtained.

Interaction of perfluorinated α-fluorosulfatocarbonyl compounds with nucleophilic reagents

Delyagina, N. I.,Avetisyan, E. A.,Rogovik, V. M.,Cherstkov, V. F.,Sterlin, S. R.,German, L. S.

, p. 217 - 222 (2007/10/02)

α-Perfluorosulfatoperfluorocarbonyl compounds interact with alkaline metals halogenides to form the corresponding α-halo derivatives as a result of the direct nucleophilic substitution of the FSO3 group.Through the action of halogenide anions on perfluorinated α,β-bis-fluorosulfatocarbonyl compounds, substitution by halogen of the FSO3 group in the α-position to the carbonyl takes place.However, the FSO3 group in the β-position is cleaved, which allows α-substituted β-dicarbonyl derivatives to be obtained.

REDUCTIVE DEFLUORINATION OF HEXAFLUOROACETONE AND THE SYNTHESIS OF HALOPENTAFLUOROACETONES

Postovoi, S. A.,Vol'pin, I. M.,Mysov, E. I.,Zeifman, Yu. V.,German, L. S.

, p. 1067 - 1070 (2007/10/02)

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