• 1. Evolutionary de novo design of phenothiazine derivatives for dye-sensitized solar cells?
  Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
• 2. Emerging 2D hybrid nanomaterials: towards enhanced sensitive and selective conductometric gas sensors at room temperature
  Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
• 3. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
• 4. Excimer and exciplex formation in a pair of bright phosphorescent isomers constructed from Cu3(pyrazolate)3 and Cu3I3 coordination luminophores?
  Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
• 5. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693

Comprehensive Overview of 1H-Imidazol-2-yl(phenyl)methanol (CAS No. 22098-62-0): Properties, Applications, and Industry Insights

1H-Imidazol-2-yl(phenyl)methanol (CAS No. 22098-62-0) is a specialized organic compound featuring a unique molecular structure combining an imidazole ring and a phenyl methanol moiety. This hybrid architecture grants it versatile chemical properties, making it valuable in pharmaceutical research, agrochemical development, and material science. With growing interest in heterocyclic compounds and bioactive intermediates, this substance has garnered attention for its potential role in designing novel enzyme inhibitors and catalysts.

The compound’s CAS number 22098-62-0 serves as a critical identifier in regulatory documentation and scientific literature. Researchers frequently explore its synthetic pathways, including reductive amination or Grignard reactions, to optimize yield and purity. Recent studies highlight its utility as a building block for N-heterocyclic carbene (NHC) ligands, which are pivotal in asymmetric catalysis—a hot topic in green chemistry initiatives.

In the pharmaceutical sector, 1H-Imidazol-2-yl(phenyl)methanol is investigated for its structural motif in drug candidates targeting inflammatory and metabolic disorders. Its imidazole core mimics natural histidine residues, enabling interactions with biological receptors. This aligns with trending searches on "imidazole-based therapeutics" and "small molecule drug discovery," reflecting industry demand for innovative scaffolds.

From an industrial perspective, the compound’s solubility in polar solvents like ethanol and DMSO enhances its applicability in formulation chemistry. Environmental concerns have spurred interest in its biodegradability profile, with computational models predicting moderate persistence—a factor crucial for sustainable chemical design. Users often query "SAFETY DATA for CAS 22098-62-0" or "suppliers of high-purity imidazole derivatives," underscoring commercial relevance.

Analytical characterization of 22098-62-0 typically involves HPLC, NMR spectroscopy, and mass spectrometry to verify structural integrity. Quality control protocols emphasize minimizing residual solvents, a priority for compliance with ICH guidelines. These details address frequent search terms like "analytical methods for imidazole alcohols" and "specification sheets for research chemicals."

Emerging applications include its use in coordination polymers and metal-organic frameworks (MOFs), where its bifunctional groups facilitate modular assembly. This intersects with nanotechnology trends, particularly queries on "functional ligands for MOF synthesis." Additionally, its derivatization potential supports combinatorial chemistry workflows, answering industry needs for diversified compound libraries.

In summary, 1H-Imidazol-2-yl(phenyl)methanol exemplifies the convergence of academic curiosity and industrial utility. Its CAS registry 22098-62-0 anchors its identity in global databases, while its adaptability meets demands across life sciences and advanced materials. As research evolves, this compound will likely remain a focal point for innovations in molecular design and sustainable chemistry.

• 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)