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24813-57-8

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24813-57-8 Usage

Organic compound

Yes

Contains

+ Two nitro groups
+ A heptafluoroisopropyl group

Attached to

Benzene ring

Common uses

+ Building block in the synthesis of pharmaceuticals
+ Building block in the synthesis of agrochemicals
+ Building block in the synthesis of industrial chemicals
+ Reagent in organic chemistry reactions

Reactivity

Highly reactive

Hazardous

Yes

Handling and storage

Should be done with care and according to safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 24813-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,1 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24813-57:
(7*2)+(6*4)+(5*8)+(4*1)+(3*3)+(2*5)+(1*7)=108
108 % 10 = 8
So 24813-57-8 is a valid CAS Registry Number.

24813-57-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-3,5-dinitrobenzene

1.2 Other means of identification

Product number -
Other names 2,4-Dinitroheptafluoroisopropylbenzene

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:24813-57-8 SDS

24813-57-8Downstream Products

24813-57-8Relevant articles and documents

Reactions Involving Fluoride Ion. Part 40. Amines as Initiators of Fluoride Ion Catalysed Reactions

Chambers, Richard D.,Gray, William K.,Korn, Stewart R.

, p. 13167 - 13176 (2007/10/03)

Tetrakis(dimethylamino)ethene (TDAE) and trimethylamine react with anhydrous unsaturated fluorocarbons to produce, 'in situ', powerful fluoride-ion sources.These are used to iniate carbon-carbon bond forming reactions eg. oligomerisation and polyfluoroalkylation, and many of these reactions occur efficiently in the absence of a solvent.

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