• 1. Evolving better nanoparticles: Genetic algorithms for optimising cluster geometries
  Dalton Trans., 2003, 4193-4207
• 2. 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
• 3. Evolution of shape, size, and areal density of a single plane of Si nanocrystals embedded in SiO2 matrix studied by atom probe tomography
  Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
• 4. 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
• 5. Enabling shape memory and healable effects in a conjugated polymer by incorporating siloxane via dynamic imine bond?
  Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Diphenylmethanes

Exploring the Potential of (3-Methoxyphenyl)(Phenyl)methanol: A Comprehensive Overview

The compound (3-Methoxyphenyl)(Phenyl)methanol, also known by its CAS registry number 13391-45-2, has garnered significant attention in the field of biomedical research due to its unique chemical structure and potential applications. This aromatic alcohol is a derivative of phenol, featuring a 3-methoxyphenyl group attached to a methanol moiety. Its intricate structure offers a range of properties that make it a subject of interest for researchers exploring natural products, pharmacology, and biotechnology.

Recent studies have highlighted the compound's antioxidant activity, which is largely attributed to its phenolic hydroxyl group and methoxy substituent. These functional groups contribute to its ability to neutralize free radicals, making it a promising candidate for applications in disease prevention and cosmeceuticals. Moreover, the presence of the 3-methoxyphenyl group introduces additional complexity to its chemical profile, potentially enhancing its bioavailability and metabolic stability.

One of the most compelling aspects of (3-Methoxyphenyl)(Phenyl)methanol is its potential role in neuroprotection. Preclinical investigations have demonstrated that this compound may possess neuroprotective properties by mitigating oxidative stress and inflammation in neural cells. This aligns with the growing interest in natural compounds as alternative therapies for neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease.

Another area of research focuses on the compound's anti-inflammatory effects. By modulating key inflammatory pathways, including COX-2 inhibition and NF-kB suppression, this aromatic alcohol exhibits potent anti-inflammatory activity. Such properties make it a valuable lead compound in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) with reduced side effects compared to conventional therapies.

Recent advancements in biomedical engineering have also explored the use of (3-Methoxyphenyl)(Phenyl)methanol as a scaffold for designing novel drug delivery systems. Its hydroxyl and methoxy groups facilitate the formation of stable conjugates with biodegradable polymers, enabling sustained release and targeted delivery of therapeutic agents. This approach holds promise for improving drug efficacy and reducing systemic toxicity.

Furthermore, the compound's photoprotective properties have been investigated in the context of skin protection against UV radiation. Its ability to absorb UV light and scavenge reactive oxygen species (ROS) generated by UV exposure makes it a potential ingredient in sunscreen formulations and cosmetic antioxidants.

In summary, (3-Methoxyphenyl)(Phenyl)methanol, with its CAS number 13391-45-2, represents a versatile compound with diverse applications across the biomedical spectrum. Its unique structure, coupled with its demonstrated antioxidant, anti-inflammatory, and neuroprotective properties, positions it as a valuable tool in drug discovery and biomedical innovation. As research continues to unravel its full potential, this aromatic alcohol is poised to play a significant role in addressing unmet medical needs and advancing personalized medicine.

• 728-87-0(4,4'-Dimethoxybenzhydrol)
• 808740-71-8(Benzenemethanol,4-methoxy-a-(4-methylphenyl)-, (aR)-)
• 23308-82-9(1-(3-Methoxyphenyl)ethanol)
• 120523-12-8((1R)-1-(3-Methoxyphenyl)ethan-1-ol)
• 129940-69-8((αS)-3-Methoxy-α-methylbenzenemethanol)
• 14950-55-1(Benzenemethanol, 3,5-dimethoxy-a-methyl-)
• 720-44-5(4-Methoxybenzhydrol)
• 808740-72-9(Benzenemethanol,4-methoxy-a-(4-methylphenyl)-, (aS)-)
• 10487-81-7(Methylium, hydroxybis(4-methoxyphenyl)-)
• 35861-33-7(Methyl, hydroxybis(4-methoxyphenyl)-)