• 1. Exceptional activity of sub-nm Pt clusters on CdS for photocatalytic hydrogen production: a combined experimental and first-principles study?
  Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
• 2. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
• 3. Emerging investigator series: heterogeneous reactions of sulfur dioxide on mineral dust nanoparticles: from single component to mixed components?
  Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
• 4. Exchangeability of amino acid residues with similar physicochemical properties in coiled-coil interactions?
  Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
• 5. 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

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Xylenols
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Xylenes Xylenols

Phenol, 2-Iodo-4,6-Dimethyl

Phenol, 2-Iodo-4,6-Dimethyl, also known by its CAS number 90003-93-3, is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound is characterized by its unique structure, which includes a phenol ring substituted with an iodo group at the 2-position and methyl groups at the 4 and 6 positions. The presence of these substituents imparts distinctive chemical and physical properties to the molecule, making it a valuable compound in both academic research and industrial applications.

The synthesis of Phenol, 2-Iodo-4,6-Dimethyl typically involves multi-step organic reactions, often starting from phenol derivatives and incorporating the iodo and methyl groups through electrophilic substitution or other suitable methods. Recent advancements in catalytic processes have enabled more efficient and selective syntheses of this compound, reducing production costs and improving yields.

In terms of physical properties, Phenol, 2-Iodo-4,6-Dimethyl exhibits a melting point of approximately 115°C and a boiling point around 285°C under standard conditions. Its solubility in common solvents such as water is relatively low due to the hydrophobic nature of the methyl groups and the electron-withdrawing effect of the iodo substituent.

One of the most notable applications of this compound is in the field of materials science, where it serves as a precursor for the synthesis of advanced polymers and high-performance materials. For instance, recent studies have demonstrated its potential in creating thermally stable polymers with excellent mechanical properties.

Moreover, Phenol, 2-Iodo-4,6-Dimethyl has found significant use in drug discovery and development processes. Its ability to act as a scaffold for bioactive molecules has led to its incorporation into various pharmacological agents targeting diseases such as cancer and neurodegenerative disorders.

The latest research on this compound has focused on its role in catalytic reactions and its potential as a building block for nanomaterials. For example, scientists have explored its use in constructing metal-organic frameworks (MOFs) with enhanced catalytic activity for environmental remediation purposes.

In conclusion, Phenol, 2-Iodo-4,6-Dimethyl is a critical compound with diverse applications across multiple disciplines. Its unique structure and properties make it an essential component in modern chemical research and industrial processes.

• 945743-56-6(1-[2-Hydroxy-3-iodo-6-(4-methylphenyl)naphthalen-1-yl]-3-iodo-6-(4-methylphenyl)naphthalen-2-ol)
• 10570-67-9(4-Iodo-2,6-dimethylphenol)
• 60577-30-2(4-Iodo-2-methylphenol)
• 549505-36-4([1,1-Biphenyl]-2,4-diol,3-iodo-(9CI))
• 2432-18-0(Phenol, 2,6-diiodo-4-methyl-)
• 24885-45-8(Phenol, 2-iodo-6-methyl-)
• 4186-52-1(2,4-diiodo-6-methylphenol)
• 23602-64-4(2-Hydroxy-3-iodobenzaldehyde)
• 388616-52-2(1,3-Benzenediol, 4-iodo-2-methyl-)
• 16188-57-1(2-Iodo-4-methylphenol)