• 1. Evolving better nanoparticles: Genetic algorithms for optimising cluster geometries
  Dalton Trans., 2003, 4193-4207
• 2. Excellent humidity sensor based on ultrathin HKUST-1 nanosheets?
  Qiaoe Wang,Meiling Lian,Xiaowen Zhu,Xu Chen RSC Adv., 2021,11, 192-197
• 3. Evolution of hierarchical porous structures in supramolecular guest–host hydrogels?
  Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
• 4. Emulsifier-free, organotellurium-mediated living radical emulsion polymerization (emulsion TERP) of styrene: poly(dimethylaminoethyl methacrylate) macro-TERP agent?
  Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
• 5. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198

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

Comprehensive Analysis of 2-Methoxy-4-phenoxyaniline (CAS No. 267416-80-8): Properties, Applications, and Industry Trends

2-Methoxy-4-phenoxyaniline (CAS No. 267416-80-8) is an organic compound with significant relevance in pharmaceutical and agrochemical research. This aniline derivative features a methoxy group and a phenoxy substituent, which contribute to its unique chemical properties. The compound's molecular formula is C₁₃H₁₃NO₂, and it is classified as an aromatic amine. Its structural characteristics make it a valuable intermediate in the synthesis of more complex molecules.

In recent years, the demand for specialty chemicals like 2-Methoxy-4-phenoxyaniline has surged due to advancements in drug discovery and material science. Researchers are particularly interested in its potential as a building block for heterocyclic compounds, which are widely used in medicinal chemistry. The compound's solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO) enhances its utility in laboratory settings.

One of the most frequently searched questions about CAS No. 267416-80-8 is its role in pharmaceutical intermediates. Studies suggest that this compound can be employed in the synthesis of bioactive molecules targeting various diseases. Additionally, its thermal stability and reactivity under controlled conditions make it suitable for catalytic reactions. These attributes align with the growing interest in sustainable chemistry and green synthesis methods.

The analytical characterization of 2-Methoxy-4-phenoxyaniline typically involves techniques such as high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR), and mass spectrometry (MS). These methods ensure the compound's purity and confirm its structural integrity. Industry professionals often search for HPLC methods for 2-Methoxy-4-phenoxyaniline to optimize their quality control processes.

Another trending topic related to this compound is its application in advanced material science. For instance, its incorporation into polymeric matrices has been explored for developing functional materials with enhanced properties. This aligns with the broader industry shift toward smart materials and nanotechnology.

From a commercial perspective, suppliers of 2-Methoxy-4-phenoxyaniline emphasize its high purity grades (e.g., ≥98%) to meet the stringent requirements of research laboratories and industrial applications. The compound is typically available in powder form, with storage recommendations highlighting protection from moisture and light to maintain stability.

In summary, 2-Methoxy-4-phenoxyaniline (CAS No. 267416-80-8) is a versatile chemical intermediate with broad applications in pharmaceuticals, agrochemicals, and material science. Its unique structural features and reactivity profile continue to attract attention from researchers and industry professionals alike. As the demand for specialized organic compounds grows, this compound is poised to play a pivotal role in future innovations.

• 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)