• 1. Excimer–monomer switch: a reaction-based approach for selective detection of fluoride?
  Qiao Song,Angela Bamesberger,Lingyun Yang,Haley Houtwed,Haishi Cao Analyst, 2014,139, 3588-3592
• 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. Fe(iii)-mediated isomerization of α,α-diarylallylic alcohols to ketones via radical 1,2-aryl migration?
  Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
• 4. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
  Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
• 5. Evolution of hierarchical porous structures in supramolecular guest–host hydrogels?
  Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847

Comprehensive Overview of 2-Bromothieno[2,3-c]furan-6(4H)-one (CAS No. 1374574-30-7)

2-Bromothieno[2,3-c]furan-6(4H)-one (CAS No. 1374574-30-7) is a heterocyclic organic compound that has garnered significant attention in pharmaceutical and materials science research. This compound belongs to the class of thienofuran derivatives, which are known for their unique electronic properties and potential applications in drug discovery. The presence of both bromine and furan moieties in its structure makes it a versatile intermediate for synthesizing more complex molecules.

Researchers are increasingly interested in 2-Bromothieno[2,3-c]furan-6(4H)-one due to its potential role in developing new therapeutic agents. Recent studies have explored its utility in creating small-molecule inhibitors for various biological targets. For instance, its structural framework is being investigated for applications in anti-inflammatory and anticancer drug development. The compound's bromine substituent also offers opportunities for further functionalization through cross-coupling reactions, a topic frequently searched by chemists in academic and industrial settings.

In the realm of materials science, 2-Bromothieno[2,3-c]furan-6(4H)-one is being studied for its potential use in organic electronics. Its conjugated system and electron-rich nature make it a candidate for organic semiconductors and photovoltaic materials. With the growing demand for sustainable energy solutions, this compound aligns with the trend of developing eco-friendly materials for solar cells and LEDs. Searches for "thienofuran-based materials" and "organic electronic intermediates" have surged in recent years, reflecting this interest.

The synthesis of 2-Bromothieno[2,3-c]furan-6(4H)-one typically involves multi-step reactions, including cyclization and bromination processes. Optimizing these synthetic routes is a common topic in organic chemistry forums and publications. Researchers often search for "efficient synthesis of brominated heterocycles" or "thienofuran derivatives preparation," highlighting the need for scalable and cost-effective methods. The compound's CAS No. 1374574-30-7 is frequently used as a reference in patents and scientific literature, underscoring its importance.

From a regulatory perspective, 2-Bromothieno[2,3-c]furan-6(4H)-one is not classified as a hazardous substance under major chemical inventories. However, proper handling and storage are recommended to ensure safety during laboratory use. This aligns with the increasing focus on green chemistry and sustainable laboratory practices, topics that resonate with modern researchers and educators.

In conclusion, 2-Bromothieno[2,3-c]furan-6(4H)-one (CAS No. 1374574-30-7) represents a promising compound with diverse applications in pharmaceuticals and advanced materials. Its unique structure and reactivity continue to inspire innovation across multiple scientific disciplines. As interest in heterocyclic chemistry and functional materials grows, this compound is poised to remain a focal point of research and development efforts worldwide.

• 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)