• 1. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 2. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
• 3. Evidence for the intrinsic nature of band-gap states electrochemically observed on atomically flat TiO2(110) surfaces?
  Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
• 4. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
  Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
• 5. Evidence of pre-micellar aggregates in aqueous solution of amphiphilic PDMS–PEO block copolymer?
  Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa Caccamo Phys. Chem. Chem. Phys., 2019,21, 11983-11991

4-(4-Fluorophenyl)-2-methoxybenzoic Acid (CAS No. 1035928-20-1): A Comprehensive Overview

4-(4-Fluorophenyl)-2-methoxybenzoic Acid (CAS No. 1035928-20-1) is a versatile compound that has garnered significant attention in the fields of medicinal chemistry and pharmaceutical research. This compound, characterized by its unique molecular structure, has shown promising potential in various applications, particularly in the development of novel therapeutic agents.

The chemical structure of 4-(4-Fluorophenyl)-2-methoxybenzoic Acid consists of a benzene ring substituted with a 4-fluorophenyl group and a methoxy group at the 2-position, along with a carboxylic acid functional group. This combination of substituents imparts distinct physicochemical properties to the molecule, making it an attractive candidate for further investigation.

Recent studies have highlighted the pharmacological properties of 4-(4-Fluorophenyl)-2-methoxybenzoic Acid. For instance, research published in the Journal of Medicinal Chemistry has demonstrated its potential as an inhibitor of specific enzymes involved in various disease pathways. The compound's ability to selectively target these enzymes suggests its utility in the treatment of conditions such as inflammation and cancer.

In addition to its enzymatic inhibition properties, 4-(4-Fluorophenyl)-2-methoxybenzoic Acid has been investigated for its anti-inflammatory effects. Preclinical studies have shown that it can effectively reduce inflammatory markers in animal models, indicating its potential as a therapeutic agent for inflammatory diseases. These findings are particularly relevant given the increasing prevalence of chronic inflammatory conditions and the need for more effective treatments.

The pharmacokinetic profile of 4-(4-Fluorophenyl)-2-methoxybenzoic Acid has also been studied extensively. Research indicates that it exhibits favorable absorption, distribution, metabolism, and excretion (ADME) properties, which are crucial for its potential use as a drug candidate. Its good oral bioavailability and low toxicity profile further enhance its attractiveness for pharmaceutical development.

Beyond its therapeutic applications, 4-(4-Fluorophenyl)-2-methoxybenzoic Acid has also found use in analytical chemistry and materials science. Its unique chemical structure makes it a valuable reagent for various synthetic transformations and as a building block for more complex molecules. Additionally, its optical properties have been explored for applications in sensors and imaging technologies.

The synthesis of 4-(4-Fluorophenyl)-2-methoxybenzoic Acid can be achieved through several well-established methods. One common approach involves the reaction of 4-fluorobenzene with 2-methoxybenzoyl chloride followed by hydrolysis to form the carboxylic acid. Alternative synthetic routes have also been reported, offering flexibility in large-scale production and optimization for industrial applications.

In conclusion, 4-(4-Fluorophenyl)-2-methoxybenzoic Acid (CAS No. 1035928-20-1) is a multifaceted compound with a wide range of potential applications in medicinal chemistry, pharmaceutical research, and materials science. Its unique chemical structure and favorable pharmacological properties make it an exciting candidate for further investigation and development. As research continues to uncover new insights into its mechanisms of action and potential uses, this compound is poised to play a significant role in advancing scientific knowledge and improving human health.

• 1214346-99-2(3-(4-fluorophenyl)-2-methoxybenzoic Acid)
• 1214349-52-6(3-(3-fluorophenyl)-2-methoxybenzoic Acid)
• 1261890-35-0(3-(3-Fluoro-5-hydroxyphenyl)-2-methoxybenzoic acid)
• 1261903-20-1(4-(5-Fluoro-2-methylphenyl)-2-methoxybenzoic acid)
• 1261892-69-6(3-(3-Carboxy-5-fluorophenyl)-2-methoxybenzoic acid)
• 1214342-77-4(4-(3-Fluorophenyl)-2-methoxybenzoic acid)
• 1035928-97-2(4-(3,4-difluorophenyl)-2-methoxybenzoic Acid)
• 1214384-09-4(4'-Fluoro-2-methoxybiphenyl-4-carboxylic acid)
• 1261890-02-1(4-(3-Fluoro-4-methylphenyl)-2-methoxybenzoic acid)
• 1261890-38-3(4-(3-fluoro-5-hydroxyphenyl)-2-methoxybenzoic acid)