• 1. Fe/S-Catalyzed synthesis of 2-benzoylbenzoxazoles and 2-quinolylbenzoxazoles via redox condensation of o-nitrophenols with acetophenones and methylquinolines?
  Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
• 2. Evolution of cellulose into flexible conductive green electronics: a smart strategy to fabricate sustainable electrodes for supercapacitors
  Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
• 3. Fate of Sb(v) and Sb(iii) species along a gradient of pH and oxygen concentration in the Carnoulès mine waters (Southern France)
  Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
• 4. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 5. Fast-pulsing NMR techniques for the detection of weak interactions: successful natural abundance probe of hydrogen bonds in peptides?
  Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzyl sulfoxides

Comprehensive Overview of 2,3-Dichloro-N-(6-methoxy-3-pyridinyl)-3-[(4-methylbenzyl)sulfinyl]acrylamide (CAS No. 1164542-94-2)

2,3-Dichloro-N-(6-methoxy-3-pyridinyl)-3-[(4-methylbenzyl)sulfinyl]acrylamide (CAS No. 1164542-94-2) is a specialized organic compound with a unique molecular structure that combines a pyridine ring, a sulfinyl group, and an acrylamide backbone. This compound has garnered significant attention in the fields of agrochemical research and pharmaceutical development due to its potential applications as an intermediate or active ingredient. Its structural complexity and functional groups make it a subject of interest for researchers exploring novel bioactive molecules and sustainable chemical solutions.

The compound’s CAS No. 1164542-94-2 serves as a unique identifier in chemical databases, ensuring precise tracking in scientific literature and patent filings. Its systematic name, 2,3-dichloro-N-(6-methoxy-3-pyridinyl)-3-[(4-methylbenzyl)sulfinyl]acrylamide, highlights key functional groups: the dichloroacrylamide moiety, which is known for its reactivity, and the methoxypyridine segment, often associated with enhanced bioavailability in drug design. The sulfinyl linker adds further versatility, enabling interactions with biological targets or catalytic systems.

In recent years, the demand for high-performance agrochemicals and eco-friendly pesticides has driven research into compounds like CAS No. 1164542-94-2. Its potential role in crop protection aligns with global trends toward sustainable agriculture, where users frequently search for terms like "green chemistry in farming" or "next-gen pesticide intermediates." Additionally, its structural features resonate with medicinal chemistry applications, particularly in the design of small-molecule inhibitors for disease targets.

From a synthetic perspective, 2,3-dichloro-N-(6-methoxy-3-pyridinyl)-3-[(4-methylbenzyl)sulfinyl]acrylamide exemplifies modern heterocyclic chemistry techniques. Researchers often explore its structure-activity relationships (SAR) to optimize properties such as solubility, stability, and target affinity. The compound’s methoxy and methylbenzyl groups are particularly noteworthy, as they influence both lipophilicity and metabolic resistance—key factors in drug discovery and agrochemical formulation.

The growing interest in AI-driven molecular design has also brought attention to compounds like CAS No. 1164542-94-2. Computational tools now enable rapid screening of its potential interactions with enzymes or receptors, addressing common search queries such as "how to predict chemical bioactivity" or "best practices for virtual screening." This intersection of computational chemistry and experimental validation underscores the compound’s relevance in contemporary research.

In summary, 2,3-dichloro-N-(6-methoxy-3-pyridinyl)-3-[(4-methylbenzyl)sulfinyl]acrylamide represents a compelling case study in multifunctional chemical design. Its applications span agricultural science, pharmaceuticals, and materials research, making it a valuable subject for further investigation. As industries prioritize sustainability and innovation, this compound’s unique attributes position it as a candidate for future breakthroughs.

• 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)