• 1. 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
• 2. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
• 3. EWOD-driven droplet microfluidic device integrated with optoelectronic tweezers as an automated platform for cellular isolation and analysis?
  Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
• 4. Examination of the hydrogen-bonding networks in small water clusters (n = 2–5, 13, 17) using absolutely localized molecular orbital energy decomposition analysis?
  Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
• 5. Fe/S-Catalyzed synthesis of 2-benzoylbenzoxazoles and 2-quinolylbenzoxazoles via redox condensation of o-nitrophenols with acetophenones and methylquinolines?
  Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020

Benzeneacetic Acid, 4-(Phenylthio)-: A Comprehensive Overview

Benzeneacetic acid, 4-(phenylthio)-, also known by its CAS number 6317-61-9, is a compound of significant interest in the fields of organic chemistry and materials science. This compound is characterized by its unique structure, which combines a benzene ring with an acetic acid group and a phenylthio substituent. The phenylthio group (-S-C6H5) introduces interesting electronic and steric properties, making this compound a valuable building block in various chemical syntheses.

The benzeneacetic acid core of this molecule serves as a versatile platform for further functionalization. Recent studies have explored its potential in drug discovery, where the phenylthio group has been shown to enhance bioavailability and stability in biological systems. For instance, researchers have investigated the use of benzeneacetic acid derivatives as inhibitors of certain enzymes involved in metabolic disorders.

In the realm of materials science, benzeneacetic acid, 4-(phenylthio)-, has been employed as a precursor for the synthesis of advanced polymers and coatings. The sulfur atom in the phenylthio group plays a crucial role in forming strong sulfur-based bonds, which contribute to the mechanical strength and thermal stability of the resulting materials. This property has led to its application in high-performance adhesives and sealants.

Recent advancements in green chemistry have also highlighted the eco-friendly synthesis routes for this compound. By utilizing catalytic processes and renewable feedstocks, chemists have developed more sustainable methods to produce benzeneacetic acid, 4-(phenylthio)-. These methods not only reduce environmental impact but also lower production costs, making the compound more accessible for industrial applications.

The long-term stability and reactivity of benzeneacetic acid, 4-(phenylthio)-, have been extensively studied under various conditions. Researchers have found that the compound exhibits excellent stability under mild conditions, making it suitable for long-term storage and transportation. However, under harsh conditions such as high temperatures or strong oxidizing agents, the phenylthio group can undergo decomposition, releasing thiophenol.

In terms of spectroscopic analysis, benzeneacetic acid, 4-(phenylthio)-, has been thoroughly characterized using techniques such as NMR (nuclear magnetic resonance) and IR (infrared spectroscopy). These studies have provided valuable insights into the electronic environment of the sulfur atom and its influence on the overall molecular structure. The presence of the benzene ring contributes to strong aromaticity, which is reflected in the distinct peaks observed in UV-Vis spectra.

Looking ahead, the potential applications of benzeneacetic acid, 4-(phenylthio)- are vast and varied. Its unique combination of properties makes it a promising candidate for use in pharmaceuticals, agrochemicals, and advanced materials. Ongoing research is focused on optimizing its synthesis pathways and exploring novel functionalization strategies to unlock even more applications.

• 1527-17-9(2-2-(Phenylthio)phenylacetic Acid)
• 54997-33-0(Benzeneacetic acid, 2-[[4-(1-methylethyl)phenyl]thio]-)
• 63349-53-1(Benzeneacetic acid, 4-(phenylthio)-, methyl ester)
• 67666-89-1(1,3-BENZENEDIACETIC ACID, 4-(PHENYLTHIO)-)
• 93012-55-6(2-(2-((6-Carboxymethylphenyl)thio)phenyl)acetic acid)
• 1334500-01-4(3-4-(Methylsulfanyl)phenylphenylacetic Acid)
• 16188-55-9(2-[4-(methylsulfanyl)phenyl]acetic acid)
• 18698-73-2(2-3-(methylsulfanyl)phenylacetic acid)
• 126585-16-8(BENZENEACETIC ACID, 4-[(4-AMINOPHENYL)THIO]-)
• 3583-58-2(2-4-(ethylsulfanyl)phenylacetic acid)