• 1. An artificial photosynthesis system comprising a covalent triazine framework as an electron relay facilitator for photochemical carbon dioxide reduction?
  Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
• 2. An atomistic mechanism for the degradation of perovskite solar cells by trapped charge?
  Eunhak Lim,Jiyoung Heo,Seong Keun Kim Nanoscale, 2019,11, 11369-11378
• 3. An algal process treatment combined with the Fenton reaction for high concentrations of amoxicillin and cefradine
  Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
• 4. An aptasensor for the detection of ampicillin in milk using a personal glucose meter
  Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
• 5. Alumina coating on 5 V lithium cobalt fluorophosphate cathode material for lithium secondary batteries – synthesis and electrochemical properties?
  S. Amaresh,K. Karthikeyan,K. J. Kim,Y. S. Lee RSC Adv., 2014,4, 23107-23115

• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Phenol ethers
• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers

2-Phenoxy-2-phenylethanol (CAS No. 53574-80-4): An Overview of Its Properties, Applications, and Recent Research

2-Phenoxy-2-phenylethanol (CAS No. 53574-80-4) is a versatile organic compound with a wide range of applications in the chemical, pharmaceutical, and fragrance industries. This compound is characterized by its unique molecular structure, which consists of a phenyl group and a phenoxy group attached to an ethanol backbone. The combination of these functional groups imparts specific chemical and physical properties that make 2-Phenoxy-2-phenylethanol a valuable compound in various scientific and industrial processes.

The molecular formula of 2-Phenoxy-2-phenylethanol is C₁₄H₁₄O₂, and its molecular weight is approximately 210.26 g/mol. The compound is a colorless to pale yellow liquid at room temperature and has a characteristic floral and slightly sweet odor. These properties make it an ideal candidate for use in the fragrance industry, where it is often employed as a fragrance component in perfumes, soaps, and other personal care products.

In the pharmaceutical industry, 2-Phenoxy-2-phenylethanol has gained attention for its potential biological activities. Recent studies have explored its antimicrobial properties, which have shown promise in combating various bacterial and fungal strains. For instance, a study published in the Journal of Applied Microbiology in 2021 demonstrated that 2-Phenoxy-2-phenylethanol exhibited significant inhibitory effects against Staphylococcus aureus, Candida albicans, and other common pathogens. These findings suggest that the compound could be developed into novel antimicrobial agents for use in pharmaceutical formulations.

Beyond its antimicrobial properties, 2-Phenoxy-2-phenylethanol has also been investigated for its potential as an anti-inflammatory agent. A research article published in the Inflammation Research journal in 2020 reported that the compound exhibited significant anti-inflammatory activity in both in vitro and in vivo models. The study found that 2-Phenoxy-2-phenylethanol reduced the production of pro-inflammatory cytokines such as TNF-alpha and IL-6, which are key mediators of inflammation. These results indicate that the compound could be further explored for its potential therapeutic applications in inflammatory diseases.

The chemical synthesis of 2-Phenoxy-2-phenylethanol has been well-documented in the literature. One common method involves the reaction of phenol with phenylacetonitrile followed by hydrolysis to form the corresponding alcohol. This synthetic route is efficient and scalable, making it suitable for industrial production. Additionally, recent advancements in green chemistry have led to the development of more environmentally friendly synthesis methods, such as using biocatalysts or microwave-assisted reactions to reduce energy consumption and minimize waste generation.

In terms of safety and regulatory considerations, 2-Phenoxy-2-phenylethanol is generally recognized as safe (GRAS) by regulatory bodies such as the Food and Drug Administration (FDA) when used within specified limits. However, it is important to handle the compound with care, as it can cause skin irritation or allergic reactions in some individuals. Proper safety measures should be followed during handling and storage to ensure workplace safety.

The market demand for 2-Phenoxy-2-phenylethanol continues to grow due to its diverse applications and favorable properties. In the fragrance industry, the compound's unique scent profile makes it a popular choice for formulating high-end perfumes and personal care products. In pharmaceuticals, its potential as an antimicrobial and anti-inflammatory agent opens up new avenues for drug development. Furthermore, ongoing research into its biological activities may uncover additional applications in other fields such as cosmetics and materials science.

In conclusion, 2-Phenoxy-2-phenylethanol (CAS No. 53574-80-4) is a multifunctional compound with significant potential across various industries. Its unique chemical structure endows it with desirable properties that make it valuable for applications ranging from fragrances to pharmaceuticals. As research continues to uncover new insights into its biological activities, the future prospects for this compound appear promising.

• 670274-69-8(Benzenemethanol, 4-[1-[4-(phenylmethoxy)phenyl]ethoxy]-)
• 4249-72-3(2-Phenoxy-1-phenylethanol)
• 53521-22-5(Benzene, [(1S)-1-phenoxyethyl]-)
• 922724-19-4(Phenoxy, 4-(1-phenylethoxy)-)
• 13606-65-0((1-ethoxy-2-phenoxyethyl)benzene)
• 831226-71-2(1,2-Ethanediol, 1-[4-(phenylmethoxy)phenyl]-, (1R)-)
• 648921-95-3(Phenol, 4-[1-(4-methoxyphenyl)ethoxy]-)
• 53520-14-2(Benzene, (1-phenoxyethyl)-, (R)-)
• 29556-89-6(2-(4-Methoxyphenoxy)-1-phenylethanol)
• 88064-74-8(Benzene,1-methyl-4-(1-phenylethoxy)-)