• 1. Dissociative dynamics of O2 on Ag(110)?
  Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
• 2. Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices
  Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
• 3. Essential effect of the electrolyte on the mechanical and chemical degradation of LiNi0.8Co0.15Al0.05O2 cathodes upon long-term cycling??
  Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
• 4. Examination of deposit in commercial diluted phosphoric acid
  Analyst, 1880,5, 146-147
• 5. Fast synthesis of copper nanoclusters through the use of hydrogen peroxide additive and their application for the fluorescence detection of Hg2+ in water samples?
  Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248

• Solvents and Organic Chemicals Organic Compounds Organosulfur compounds Thioethers Aryl thioethers

Comprehensive Overview of N-(3-methylbutan-2-yl)-2-(methylsulfanyl)aniline (CAS No. 1154296-78-2)

N-(3-methylbutan-2-yl)-2-(methylsulfanyl)aniline (CAS No. 1154296-78-2) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research, agrochemical development, and material science. This compound, characterized by its unique aniline derivative structure, is often explored for its potential applications in drug discovery and catalysis. Researchers are particularly interested in its sulfanyl group, which may contribute to its reactivity and binding properties in biological systems.

The compound's molecular structure features a methylsulfanyl substituent attached to an aniline backbone, coupled with a branched 3-methylbutan-2-yl group. This combination of functional groups makes it a versatile intermediate in organic synthesis. Recent studies have highlighted its potential role in the development of novel therapeutics, particularly in targeting enzyme inhibition and receptor modulation. Its lipophilic nature also suggests potential applications in drug delivery systems.

In the context of green chemistry, N-(3-methylbutan-2-yl)-2-(methylsulfanyl)aniline has been investigated for its potential as a sustainable catalyst or ligand in environmentally friendly reactions. The growing demand for eco-friendly synthetic routes has driven research into compounds like this, which may reduce reliance on hazardous reagents. Additionally, its structural analogs have been explored in polymer chemistry, where they contribute to the development of high-performance materials.

From a commercial perspective, the compound's CAS No. 1154296-78-2 is frequently searched in databases by chemical suppliers and research institutions. Its availability and purity standards are critical for reproducibility in experiments. The compound is often compared to other aniline derivatives, such as N-alkyl anilines or thioether-containing compounds, due to their shared applications in medicinal chemistry.

One of the most frequently asked questions about N-(3-methylbutan-2-yl)-2-(methylsulfanyl)aniline revolves around its synthetic pathways. Researchers often seek optimized methods for its preparation, including one-pot reactions or microwave-assisted synthesis. Another hot topic is its toxicity profile, as understanding its biological safety is essential for preclinical studies. The compound's stability under various conditions is also a key consideration for industrial applications.

In summary, N-(3-methylbutan-2-yl)-2-(methylsulfanyl)aniline (CAS No. 1154296-78-2) represents a promising area of research with diverse applications. Its structural versatility and potential in drug development and material science make it a compound of significant interest. As the scientific community continues to explore its properties, it is likely to remain a focal point in organic chemistry and applied research.

• 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)