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3-Chloro-2,6-difluorobenzoic acid is a fluorinated benzoic acid derivative with the molecular formula C7H3ClF2O2. It features a chloro substituent at the 3-position and two fluorine atoms at the 2and 6-positions on the benzene ring. This white crystalline solid is slightly soluble in water and serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its functional and structural properties also make it a valuable building block in organic synthesis and a reagent in chemical research, with potential applications in material science and polymer chemistry.

225104-76-7

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225104-76-7 Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-2,6-difluorobenzoic acid is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structural properties allow for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 3-chloro-2,6-difluorobenzoic acid is utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its presence in these compounds can enhance their performance and selectivity in controlling pests and weeds.
Used in Dye Industry:
3-Chloro-2,6-difluorobenzoic acid is used as a key intermediate in the production of various dyes. Its incorporation into dye molecules can result in improved color properties and stability.
Used in Organic Synthesis:
As a building block in organic synthesis, 3-chloro-2,6-difluorobenzoic acid is used to construct a wide range of organic compounds. Its functional groups and structural features facilitate the formation of diverse chemical entities for various applications.
Used in Chemical Research:
3-Chloro-2,6-difluorobenzoic acid serves as a reagent in chemical research, enabling the exploration of new reaction pathways and the development of innovative synthetic methods.
Used in Material Science and Polymer Chemistry:
Due to its functional and structural properties, 3-chloro-2,6-difluorobenzoic acid has potential applications in the field of material science and polymer chemistry. It can be incorporated into polymers to impart specific properties, such as enhanced thermal stability, mechanical strength, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 225104-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,1,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 225104-76:
(8*2)+(7*2)+(6*5)+(5*1)+(4*0)+(3*4)+(2*7)+(1*6)=97
97 % 10 = 7
So 225104-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClF2O2/c8-3-1-2-4(9)5(6(3)10)7(11)12/h1-2H,(H,11,12)

225104-76-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B23893)  3-Chloro-2,6-difluorobenzoic acid, 97%   

  • 225104-76-7

  • 1g

  • 559.0CNY

  • Detail
  • Alfa Aesar

  • (B23893)  3-Chloro-2,6-difluorobenzoic acid, 97%   

  • 225104-76-7

  • 5g

  • 2115.0CNY

  • Detail
  • Alfa Aesar

  • (B23893)  3-Chloro-2,6-difluorobenzoic acid, 97%   

  • 225104-76-7

  • 10g

  • 3616.0CNY

  • Detail

225104-76-7SDS

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 3-CHLORO-2,6-DIFLUOROBENZOIC ACID

1.2 Other means of identification

Product number -
Other names 3-Chloro-2,6-difluoro-Benzoicacid

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:225104-76-7 SDS

225104-76-7Relevant academic research and scientific papers

Direct C–H Carboxylation Forming Polyfunctionalized Aromatic Carboxylic Acids by Combined Br?nsted Bases

Hanasaka, Kazuya,Izumi, Koki,Kondo, Yoshinori,Kwon, Eunsang,Nozawa-Kumada, Kanako,Shigeno, Masanori,Tohara, Itsuki,Yamakoshi, Hiroyuki

supporting information, p. 809 - 814 (2022/02/05)

CO2 fixation into electron-deficient aromatic C–H bonds proceeds with the combined Br?nsted bases LiO-t-Bu and LiO-t-Am/CsF/18-crown-6 (t-Am = CEtMe2) under a CO2 atmosphere to afford a variety of polyfunctionalized aromat

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