22509-50-8 Usage
Description
2,6-dichloro-4-nitrobenzoic acid is a chemical compound characterized by its molecular formula C7H3Cl2NO4. It is a yellow crystalline solid known for its high reactivity and stability, commonly utilized in organic synthesis and as an intermediate in the production of pharmaceuticals and dyes.
Uses
Used in Organic Synthesis:
2,6-dichloro-4-nitrobenzoic acid is used as a key intermediate for the synthesis of various organic compounds, leveraging its reactivity to form new chemical entities.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2,6-dichloro-4-nitrobenzoic acid is used as a precursor in the manufacturing process of certain drugs, contributing to the development of new medicinal agents.
Used in Dye Production:
2,6-dichloro-4-nitrobenzoic acid is also employed in the production of dyes, where its chemical properties are harnessed to create a range of colorants for various applications.
Used as a Reagent:
2,6-dichloro-4-nitrobenzoic acid serves as a reagent in the preparation of different compounds, facilitating chemical reactions in research and industrial settings.
Used in Antimicrobial Applications:
2,6-dichloro-4-nitrobenzoic acid has been studied for its potential as an antifungal and antibacterial agent, showing promise in inhibiting the growth of certain pathogens, thereby contributing to the field of microbiology and infectious disease control.
Used in Material Development:
2,6-dichloro-4-nitrobenzoic acid's properties are being explored for potential uses in the development of new materials, indicating its versatility and applicability in advancing material sciences.
Check Digit Verification of cas no
The CAS Registry Mumber 22509-50-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,5,0 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22509-50:
(7*2)+(6*2)+(5*5)+(4*0)+(3*9)+(2*5)+(1*0)=88
88 % 10 = 8
So 22509-50-8 is a valid CAS Registry Number.
22509-50-8Relevant articles and documents
A convenient synthesis of a lymphocyte function-associated antigen-1 (LFA-1) antagonist of 'Compound 4'
Xu, Sheng,Zhou, Guo-Chun
, p. 280 - 284 (2018/06/27)
The lymphocyte function-associated antigen-1 (LFA-1) antagonist of 'Compound 4' was synthesised by a convenient route using cheap, commercially available starting materials and catalysts under mild reaction conditions and by easily handled reactions. The total yield in the preparation of 'Compound 4' was more than 38% via Sonogashira coupling of an iodide and an alkyne, reduction of the alkyne catalysed by Raney nickel and later steps involving hydrolysis of an ester, condensation of an acid and an amine and a final hydrolysis of an ester.
Preparation of fluorous Yamaguchi reagents and evaluation of their reactivity in esterification
Nishio, Yuya,Kawazu, Akari,Hirano, Shun,Matsubara, Hiroshi
, p. 720 - 725 (2016/01/15)
Fluorous Yamaguchi (FY) reagents bearing a perfluoroalkyl chain were prepared and employed in esterification reactions; the yields were similar to those obtained with the traditional Yamaguchi (TY) reagent. Fluorous benzoic acids derived from the FY reagents were separated easily after the reaction. GC analysis revealed that the initial rates of reaction with the FY reagents were higher than those with the TY reagent. The acidities of benzoic acids produced from the FY and TY reagents were predicted by DFT to be similar (1.20 and 0.96, respectively).
TRIAZOLE COMPOUNDS AS ANTIVIRALS
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Paragraph 0337, (2014/01/18)
The present invention discloses compounds of Formula I: wherein the variables in Formula I are defined as described herein. Also disclosed are pharmaceutical compositions containing such compounds and methods for using the compounds of Formula I in the prevention or treatment of HCV infection.
