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  Analyst, 1966,91, 208-210
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  Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
• 3. An atlas of endohedral Sc2S cluster fullerenes?
  Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
• 4. An atomic scale study of defects in Co2FeAl
  Ravi Kumar Yadav,R. Govindaraj Phys. Chem. Chem. Phys., 2020,22, 26876-26886
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Biphenyls and derivatives Chlorinated biphenyls

2-(4-Carboxy-3-fluorophenyl)-6-chlorobenzoic Acid: A Comprehensive Overview

2-(4-Carboxy-3-fluorophenyl)-6-chlorobenzoic acid, identified by the CAS number 1261964-27-5, is a complex organic compound with significant potential in various fields of chemistry and materials science. This compound is characterized by its unique structure, which includes a benzoic acid moiety substituted with a fluorine atom at the 3-position and a chlorine atom at the 6-position, along with a carboxy group at the 4-position of the phenyl ring. These substituents contribute to its distinctive chemical properties and reactivity.

The synthesis of 2-(4-Carboxy-3-fluorophenyl)-6-chlorobenzoic acid involves multi-step reactions, often starting from fluorobenzene derivatives and progressing through various substitution and oxidation processes. Recent advancements in synthetic methodologies have enabled more efficient and selective routes to this compound, reducing production costs and minimizing environmental impact. Researchers have also explored the use of microwave-assisted synthesis and catalytic systems to optimize reaction conditions, making this compound more accessible for large-scale applications.

In terms of applications, 2-(4-Carboxy-3-fluorophenyl)-6-chlorobenzoic acid has shown promise in pharmaceutical research as a potential lead compound for drug development. Its structure allows for interactions with various biological targets, including enzymes and receptors, making it a valuable tool in medicinal chemistry. Additionally, this compound has been investigated for its role in polymer chemistry, where it serves as a building block for advanced materials with tailored properties such as improved thermal stability and mechanical strength.

Recent studies have focused on the electrochemical properties of 1261964-27-5, revealing its potential as an active material in energy storage devices such as supercapacitors and batteries. The presence of electron-withdrawing groups like chlorine and fluorine enhances its redox activity, making it a candidate for high-performance energy storage solutions. Furthermore, computational modeling techniques have been employed to predict its electronic structure and reactivity, providing insights into its behavior under different conditions.

The environmental impact of synthesizing and using 2-(4-Carboxy-3-fluorophenyl)-6-chlorobenzoic acid has also been a topic of interest. Researchers are exploring green chemistry approaches to minimize waste generation and improve sustainability in its production processes. This includes the use of biodegradable solvents, recyclable catalysts, and energy-efficient reaction conditions.

In conclusion, 2-(4-Carboxy-3-fluorophenyl)-6-chlorobenzoic acid, with its CAS number 1261964-27-5, represents a versatile compound with diverse applications across multiple disciplines. Ongoing research continues to uncover new potential uses while addressing challenges related to synthesis efficiency and environmental sustainability.

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• 1261964-19-5(4-(4-Carboxy-3-fluorophenyl)-2-chlorobenzoic acid)
• 1261892-91-4(2-(2,3-dichlorophenyl)-6-fluorobenzoic Acid)
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• 1261970-07-3(2-(3-Chloro-2-methylphenyl)-6-fluorobenzoic acid)
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