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2338-64-9

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2338-64-9 Usage

Uses

1,1,2,2,3,3-Hexafluoroindene is used as an electrolyte for secondary battery.

Check Digit Verification of cas no

The CAS Registry Mumber 2338-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,3 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2338-64:
(6*2)+(5*3)+(4*3)+(3*8)+(2*6)+(1*4)=79
79 % 10 = 9
So 2338-64-9 is a valid CAS Registry Number.

2338-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3-hexafluoroindene

1.2 Other means of identification

Product number -
Other names 1,1,2,2,3,3-hexafluoro-2,3-dihydro-1H-indene

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:2338-64-9 SDS

2338-64-9Downstream Products

2338-64-9Relevant articles and documents

-

Platonov,V.E.,Yakobson,G.G.

, p. 374 - 384 (1976)

-

THERMOLYTIC TRANSFORMATION OF POLYFLUORINATED ORGANIC COMPOUNDS. XXVIII. PRODUCTION OF POLYFLUOROINDANES AND SOME OF THEIR CHARACTERISTICS

Platonov, V. E.,Malyuta, N. G.,Yakobson, G. G.

, p. 345 - 353 (2007/10/02)

The copyrolysis (620 deg C) of phenol and ortho- and para-halogenophenols with perfluoroethylene in a flow-type system was investigated. 1,1,2,2,3,3-hexafluoroindane was mostly obtained from phenol, anisole, and o-bromophenol; o-chlorophenol gives the same compounds as the main product together with 1,1,2,2,3,3-hexafluoro-4-chloroindane; in the case of o-fluorophenol the main reaction products are 1,1,2,2,3,3-hexafluoroindane and 1,1,2,2,3,3,4- and 1,1,2,2,3,3,5-heptafluoroindanes.With perfluoroethylene para-halogenophenols form 1,1,2,2,3,3-hexafluoro-5-halogenoindanes.The paths to the formation of the polyfluoroindanes are discussed.When heated with nitric acid, 1,1,2,2,3,3-hexafluoroindane gives mainly 4-nitro-1,1,2,2,3,3-hexafluoroindane, from which the corresponding amino derivative is obtained by reduction.

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