• 1. Emerging enantiomeric resolution materials with homochiral nano-fabrications
  Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
• 2. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
  Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
• 3. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
• 4. Empowering microfluidics by micro-3D printing and solution-based mineral coating?
  Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
• 5. Dissociative dynamics of O2 on Ag(110)?
  Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445

3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid: A Comprehensive Overview

The compound 3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid, identified by the CAS number 1261902-10-6, is a significant molecule in the field of organic chemistry and pharmacology. This compound has garnered attention due to its unique structural properties and potential applications in drug discovery and material science. Recent studies have highlighted its role in various biological systems, making it a subject of interest for researchers worldwide.

The molecular structure of 3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid consists of a benzoic acid moiety with specific substituents that confer unique electronic and steric properties. The presence of a methoxy group at the 5-position and a chloromethylphenyl group at the 3-position introduces significant electronic effects, which influence its reactivity and bioavailability. These structural features make it a versatile building block for synthesizing more complex molecules with tailored functionalities.

Recent advancements in synthetic methodologies have enabled the efficient synthesis of 3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid. Researchers have explored various routes, including Suzuki coupling reactions and Friedel-Crafts acylation, to optimize its production. These methods not only enhance yield but also ensure high purity, which is critical for its application in pharmaceuticals and biotechnology.

The biological activity of 3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid has been extensively studied in recent years. Experimental data indicate that this compound exhibits potent anti-inflammatory and antioxidant properties, making it a promising candidate for developing therapeutic agents against chronic diseases such as neurodegenerative disorders and cardiovascular conditions. Additionally, its ability to modulate key cellular pathways has been documented in preclinical models, further underscoring its potential in drug development.

In the context of material science, 3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid has been investigated for its role in creating advanced materials with tailored electronic properties. Its incorporation into polymer frameworks has shown promise in enhancing conductivity and mechanical stability, which could lead to innovative applications in electronics and energy storage systems.

The synthesis and characterization of 3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid have been supported by cutting-edge analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. These tools provide detailed insights into its molecular structure and purity, ensuring reliability in both academic research and industrial applications.

In conclusion, 3-(4-Chloro-3-methylphenyl)-5-methoxybenzoic acid, with its distinctive chemical properties and diverse applications, continues to be a focal point in scientific research. As ongoing studies unravel its full potential, this compound is poised to make significant contributions to fields ranging from medicine to materials science.

• 892843-81-1([1,1'-Biphenyl]-4-carboxylicacid, 2'-chloro-4'-methoxy-)
• 1261992-00-0(2-Chloro-4-(3,5-dimethoxyphenyl)benzoic acid)
• 1179607-85-2(2-chloro-5-(3-methoxyphenyl)benzoic Acid)
• 1215205-42-7(2'-Chloro-5'-methoxybiphenyl-3-carboxylic acid)
• 1181567-17-8(4-Chloro-3-(4-methoxyphenyl)benzoic acid)
• 1262007-22-6(3-(2,5-Dichlorophenyl)-5-methoxybenzoic acid)
• 1237071-49-6(2-Chloro-4-(3-methoxyphenyl)benzoic acid)
• 1261956-12-0(2-chloro-4-(2-chloro-5-methoxyphenyl)benzoic Acid)
• 1181609-23-3(4-chloro-3-(3-methoxyphenyl)benzoic Acid)
• 1261992-55-5(2-chloro-5-(2-chloro-5-methoxyphenyl)benzoic Acid)