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773873-26-0

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773873-26-0 Usage

Description

2,3-DIFLUORO-4-METHOXYBENZOIC ACID is a chemical compound with the formula C8H6F2O3, belonging to the benzoic acid derivatives. It features two fluorine atoms and one methoxy group, contributing to its unique chemical properties. This white crystalline solid has a melting point of approximately 118-120°C and exhibits limited solubility in water. Due to its potential to cause irritation to the skin, eyes, and respiratory system, careful handling is advised.

Uses

Used in Pharmaceutical Industry:
2,3-DIFLUORO-4-METHOXYBENZOIC ACID is utilized as a building block in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, making it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-DIFLUORO-4-METHOXYBENZOIC ACID serves as a key intermediate in the production of pesticides and other agrochemicals. Its incorporation can enhance the effectiveness of these products and contribute to agricultural productivity.
Used in Specialty Chemicals Production:
2,3-DIFLUORO-4-METHOXYBENZOIC ACID is also employed as an intermediate in the manufacturing of specialty chemicals. Its distinctive chemical characteristics enable the creation of high-value compounds for use in various industries, such as materials science and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 773873-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,8,7 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 773873-26:
(8*7)+(7*7)+(6*3)+(5*8)+(4*7)+(3*3)+(2*2)+(1*6)=210
210 % 10 = 0
So 773873-26-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6F2O3/c1-13-5-3-2-4(9)7(10)6(5)8(11)12/h2-3H,1H3,(H,11,12)

773873-26-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H26830)  2,3-Difluoro-6-methoxybenzoic acid, 97%   

  • 773873-26-0

  • 1g

  • 824.0CNY

  • Detail
  • Alfa Aesar

  • (H26830)  2,3-Difluoro-6-methoxybenzoic acid, 97%   

  • 773873-26-0

  • 10g

  • 4754.0CNY

  • Detail

773873-26-0SDS

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 2,3-Difluoro-6-methoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 2,3-difluoro-6-methoxybenzoic acid

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:773873-26-0 SDS

773873-26-0Downstream Products

773873-26-0Relevant articles and documents

Preparation method for 2, 3-difluoro-6-methoxy benzoic acid

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Paragraph 0030; 0033-0036; 0039-0042; 0045-0048; 0051-0054, (2017/02/28)

The invention provides a preparation method for 2, 3-difluoro-6-methoxy benzoic acid. The preparation method includes the steps: (1) preparing tetrahydrofuran solution of lithium diisopropylamide; (2) reducing temperature to range from -75 DEG C to -65 DE

PYRAZOLE DERIVATIVES FOR THE INHIBITION OF CDK' S AND GSK' S

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Page/Page column 148, (2008/06/13)

The invention provides compounds of the formula (I), or salts, tautomers, N-oxides or solvates thereof wherein: R1 is selected from: (a) 2,6-dichlorophenyl; (b) 2,6-difluorophenyl; (c) a 2,3,6-trisubstituted phenyl group wherein the substituents for the phenyl group are selected from fluorine, chlorine, methyl and methoxy; (d) a group R0; (e) a group R a; (f) a group Rlb; (g) a group Rlc; (h) a group Rld; and 0) 2,6-difluorophenylamino ; wherein R )0υ, r R> llaa, T Rj I1bD, T R) I1cC, r R> Iidα, r R?2zaa, r R>22bD and RJ are as defined in the claims. The compounds have activity as inhibitors of cdk kinase (such as cdkl or cdk2) and glycogen synthase kinase-3 activity.

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