• 1. Evolution study of photo-synthesized gold nanoparticles by spectral deconvolution model: a quantitative approach
  Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
• 2. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 3. Enabling stable MnO2 matrix for aqueous zinc-ion battery cathodes?
  Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
• 4. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 5. Excess electrons in lithium–ethylamine solutions—density, electrical conductivity and EPR studies
  Phys. Chem. Chem. Phys., 1999,1, 3561-3565

Introduction to 4-(4-Phenoxyphenyl)Butanoic Acid (CAS No. 6958-94-7)

4-(4-phenoxyphenyl)butanoic acid, also known by its CAS registry number CAS No. 6958-94-7, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound, with its unique structure and properties, has been the subject of extensive research in recent years, particularly in the context of drug discovery and development.

The molecular structure of 4-(4-phenoxyphenyl)butanoic acid consists of a butanoic acid backbone attached to a phenoxyphenyl group. This arrangement imparts the compound with both hydrophilic and hydrophobic characteristics, making it suitable for various applications. The phenoxy group, in particular, is known for its ability to enhance the solubility and bioavailability of molecules, which is a critical factor in drug design.

Recent studies have highlighted the potential of 4-(4-phenoxyphenyl)butanoic acid as a precursor or intermediate in the synthesis of bioactive compounds. For instance, researchers have explored its role in the development of anti-inflammatory agents and antioxidants. The compound's ability to interact with cellular pathways involved in inflammation and oxidative stress has been a focal point of these investigations.

In terms of synthesis, 4-(4-phenoxyphenyl)butanoic acid can be prepared through several methods, including nucleophilic aromatic substitution and coupling reactions. These methods have been optimized to improve yield and purity, ensuring that the compound meets the high standards required for pharmaceutical applications.

The physical properties of 4-(4-phenoxyphenyl)butanoic acid are also noteworthy. It has a melting point of approximately 120°C and is sparingly soluble in water but dissolves readily in organic solvents such as dichloromethane and ethyl acetate. These properties make it amenable to various analytical techniques, including high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy.

One of the most promising areas of research involving CAS No. 6958-94-7 is its potential use in targeted drug delivery systems. Scientists have investigated its ability to serve as a carrier molecule for delivering therapeutic agents to specific tissues or cells. This application leverages the compound's biocompatibility and its ability to encapsulate or conjugate with drugs without compromising their efficacy.

In addition to its pharmacological applications, 4-(4-phenoxyphenyl)butanoic acid has also been studied for its role in materials science. Researchers have explored its use as a building block for creating novel polymers and surfactants. These materials exhibit unique properties, such as enhanced stability and biodegradability, which could be valuable in industries ranging from packaging to biomedical engineering.

The environmental impact of CAS No. 6958-94-7 is another area that has garnered attention. Studies have assessed its biodegradability under various conditions, with findings suggesting that it can be effectively metabolized by microorganisms in aqueous environments. This characteristic is particularly important for ensuring that the compound does not persist as an environmental pollutant.

In conclusion, 4-(4-phenoxyphenyl)butanoic acid, identified by its CAS registry number CAS No. 6958-94-7, is a versatile compound with a wide range of potential applications. From drug discovery to materials science, ongoing research continues to uncover new ways to harness its unique properties for beneficial purposes.

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)