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Diethyl 2,3-difluorosuccinate is a chemical compound with the molecular formula C6H8F2O4. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 192.12 g/mol. diethyl 2,3-difluorosuccinate is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique difluorinated succinate structure. It can be synthesized through various methods, such as the reaction of diethyl succinate with a fluorinating agent like diethylaminosulfur trifluoride (DAST) or the use of a fluorinating catalyst. Diethyl 2,3-difluorosuccinate is known for its reactivity and stability, making it a valuable building block in the development of new compounds with potential applications in various industries.

868-24-6

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868-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868-24-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 868-24:
(5*8)+(4*6)+(3*8)+(2*2)+(1*4)=96
96 % 10 = 6
So 868-24-6 is a valid CAS Registry Number.

868-24-6SDS

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 diethyl 2,3-difluorosuccinate

1.2 Other means of identification

Product number -
Other names α,α'-Difluorbernsteinsaeure-diethylester

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:868-24-6 SDS

868-24-6Downstream Products

868-24-6Relevant academic research and scientific papers

Synthesis of 2′,3′-dideoxy-2′-fluoro-4′- thionucleosides from a fluoroxanthate

Jean-Baptiste, La?titia,Lefebvre, Pierre,Pfund, Emmanuel,Lequeux, Thierry

, p. 817 - 820 (2008)

The synthesis of a thiobutyrolactone as precursor of modified nucleosides is reported from a fluoroxanthate and a protected allylic alcohol. This approach opens a new and straightforward route for the synthesis of 2′,3′- dideoxy-2′-fluoro-4′-thiothymidine derivatives in few steps, including the formation of a fluorothiolactone and a Vorbrüggen thymine base alkylation reaction. Georg Thieme Verlag Stuttgart.

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