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Difluoro-Propanedioicacid, also known as 2,2-Difluorosuccinic acid, is a fluorinated derivative of succinic acid with the chemical formula C3H2F2O4. It is a di-carboxylic acid that contains two carboxylic acid functional groups. difluoro-Propanedioicacid is characterized by its unique properties and is utilized as an intermediate in various chemical syntheses.

1514-85-8

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1514-85-8 Usage

Uses

Used in Pharmaceutical Synthesis:
Difluoro-Propanedioicacid is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of novel drug molecules. Its unique properties allow it to be incorporated into the structures of potential therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, difluoro-Propanedioicacid serves as an intermediate in the production of various agrochemicals, contributing to the development of effective and targeted pest control solutions.
Used in Specialty Chemicals Synthesis:
Difluoro-Propanedioicacid is utilized as an intermediate in the synthesis of specialty chemicals, where its specific properties can enhance the performance or characteristics of the final products.
Used in Polymer Production:
difluoro-Propanedioicacid is also used in the production of polymers, where it can influence the polymer's properties, such as strength, flexibility, or chemical resistance.
Used as a Building Block in Organic Chemistry:
Difluoro-Propanedioicacid has potential applications in the field of medicinal chemistry and drug discovery, acting as a building block for the creation of complex organic molecules with potential therapeutic uses.

Check Digit Verification of cas no

The CAS Registry Mumber 1514-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1514-85:
(6*1)+(5*5)+(4*1)+(3*4)+(2*8)+(1*5)=68
68 % 10 = 8
So 1514-85-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H2F2O4/c4-3(5,1(6)7)2(8)9/h(H,6,7)(H,8,9)

1514-85-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-difluoropropanedioic acid

1.2 Other means of identification

Product number -
Other names Propanedioic acid,difluoro-(9CI)

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:1514-85-8 SDS

1514-85-8Relevant academic research and scientific papers

REACTIONS OF PERHALOCARBONS. PART IX. CONVERSION OF PER(POLY)FLUOROALKYL HALIDES INTO THE CORRESPONDING CARBOCYCLIC ACIDS WITH A REDOX SYSTEM

Hu, Chang-Ming,Qing, Feng-Ling,Zhang, Hong-Gen

, p. 275 - 280 (1990)

The conversion of per(poly)fluoroalkylhalides into the corresponding carbocyclic acids with a redox system-(NH4)2S2O8/HCO2Na is described.The reaction provides a convenient method for the synthesis of various per(poly)fluorocarboxylic acids under mild conditions.

METHODS OF MAKING POLYFUNCTIONAL POLYFLUORINATED COMPOUNDS

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Page/Page column 21-23, (2019/07/13)

A method of making a polyfunctional polyfluorinated compound includes combining first components that include a polyfluorinated cyclic compound having 4 to 7 ring carbon atoms and at least one of osmium tetroxide, ruthenium tetroxide or a precursor thereof and forming a polyfluorinated dicarboxylic acid. Two of the ring carbon atoms of the polyfluorinated cyclic compound form a double bond or an epoxide. The precursor reacts with an oxidant to form ruthenium tetroxide. Methods also include converting the polyfluorinated dicarboxylic acid to a polyfluorinated dicarboxylic acid halide and converting the polyfluorinated dicarboxylic acid halide to other polyfunctional polyfluorinated compounds.

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