• 1. An integrated process of CO2 capture and in situ hydrogenation to formate using a tunable ethoxyl-functionalized amidine and Rh/bisphosphine system?
  Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
• 2. An aptasensor for detection of potassium ions based on RecJf exonuclease mediated signal amplification
  Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
• 3. An air-stable organometallic polymer containing titanafluorene moieties obtained by the Sonogashira–Hagihara cross-coupling polycondensation?
  Alvin Tanudjaja,Shinsuke Inagi,Fusao Kitamura,Toshikazu Takata,Ikuyoshi Tomita Dalton Trans., 2021,50, 3037-3043
• 4. An astrophysically-relevant mechanism for amino acid enantiomer enrichment
  Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
• 5. An artificial blood vessel implanted three-dimensional microsystem for modeling transvascular migration of tumor cells?
  Xue-Ying Wang,Ying Pei,Min Xie,Zi-He Jin,Ya-Shi Xiao,Yang Wang,Li-Na Zhang,Yan Li,Wei-Hua Huang Lab Chip, 2015,15, 1178-1187

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Phenylacetylindoles

Exploring the Chemistry and Applications of 1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone (CAS No. 1097087-10-9)

1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone (CAS No. 1097087-10-9) is a specialized organic compound that has garnered significant interest in pharmaceutical and biochemical research. This compound, which features an indole core linked to a methoxyphenyl group via an ethanone bridge, exhibits unique structural properties that make it valuable for various applications. Researchers are particularly intrigued by its potential role in drug discovery and medicinal chemistry, as its molecular framework is often associated with bioactive molecules.

The synthesis of 1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone involves multi-step organic reactions, including Friedel-Crafts acylation and indole functionalization. Its CAS No. 1097087-10-9 serves as a unique identifier in chemical databases, facilitating its study and procurement. The compound's molecular weight and solubility properties are critical for its application in high-throughput screening and biochemical assays. Recent studies have explored its interactions with enzyme targets, suggesting potential utility in therapeutic development.

One of the most compelling aspects of 1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone is its relevance in neuropharmacology. The indole moiety is a common feature in compounds that modulate serotonin receptors, making this molecule a candidate for research into neurological disorders. Additionally, its methoxyphenyl group may contribute to blood-brain barrier permeability, a key factor in CNS drug design. These attributes align with current trends in precision medicine and targeted therapy, which are hot topics in the scientific community.

Beyond pharmaceuticals, 1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone has applications in material science. Its conjugated system and aromatic rings make it a potential candidate for organic electronics, such as OLEDs and photovoltaic devices. Researchers are also investigating its use as a fluorescent probe due to its photophysical properties. These interdisciplinary applications highlight the versatility of this compound, addressing growing interest in sustainable technologies and green chemistry.

The market for 1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone is expanding, driven by demand from research institutions and pharmaceutical companies. Its CAS No. 1097087-10-9 is frequently searched in chemical databases, reflecting its importance in academic and industrial settings. Suppliers often highlight its high purity and custom synthesis options to meet diverse research needs. As AI-driven drug discovery gains traction, compounds like this are increasingly valuable for virtual screening and molecular modeling.

In summary, 1-(1H-Indol-3-yl)-2-(2-methoxyphenyl)ethanone (CAS No. 1097087-10-9) is a multifaceted compound with significant potential in drug development, material science, and biochemical research. Its unique structure and properties align with cutting-edge trends such as neuropharmacology, organic electronics, and AI-assisted chemistry. For researchers seeking innovative solutions, this molecule offers a promising avenue for exploration and innovation.

• 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)