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142453-19-8

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142453-19-8 Usage

Structure

A thiophene ring with two adjacent carbon atoms replaced by oxygen atoms, forming a cyclic diketone structure. Two fluorine atoms are substituted at positions 3 and 4 of the thiophene ring.

Type of compound

A chemical compound used in organic synthesis.

Applications

Can act as a building block for the construction of various organic molecules and materials. Has potential applications in medicinal chemistry and pharmaceutical research.

Additional information

Further research is needed to fully explore its potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 142453-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,5 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142453-19:
(8*1)+(7*4)+(6*2)+(5*4)+(4*5)+(3*3)+(2*1)+(1*9)=108
108 % 10 = 8
So 142453-19-8 is a valid CAS Registry Number.

142453-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name difluoro-2,5-dihydrothiophene-2,5-dione

1.2 Other means of identification

Product number -
Other names -

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:142453-19-8 SDS

142453-19-8Downstream Products

142453-19-8Relevant articles and documents

Process for the preparation of difluoromaleic anhydride

-

, (2008/06/13)

A process for producing difluoromaleic anhydride by reacting sulfur trioxide with a fluorinated precursor selected from the group consisting of hexafluoro-2,5-dihydrofuran, hexafluoro-2,5-dihydrothiophene, difluoro-2,5-dihydrothiophene-2,5-dione and tetrafluoro-2,5-dihydrothiophene-2-one. Also disclosed are the compounds difluoro-2,5-dihydrothiophene-2,5-dione and tetrafluoro-2,5-dihydrothiophene-2-one. Difluoromaleic anhydride is useful for example as a component of fluoropolymers.

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