• 1. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
  Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
• 2. An intermolecular C–C coupling reaction of iridium complexes?
  Kathrin Kutlescha,Rhett Kempe New J. Chem., 2010,34, 1954-1960
• 3. An antioxidative galactomannan extracted from Chinese Sesbania cannabina enhances immune activation of macrophage cells?
  Chongyang Zhu,Xiaojia Bian,Xin Jia,Ning Tang,Yongqiang Cheng Food Funct., 2020,11, 10635-10644
• 4. An anti-leakage liquid metal thermal interface material
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• 5. An amorphous carbon nitride/NiO/CoN-based composite: a highly efficient nonprecious electrode for supercapacitors and the oxygen evolution reaction?
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• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Ketones
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Carbonyl compounds Ketones

Comprehensive Overview of Ethanone, 2-hydroxy-1-(2-thienyl)- (CAS No. 88511-88-0): Properties, Applications, and Industry Insights

Ethanone, 2-hydroxy-1-(2-thienyl)- (CAS No. 88511-88-0) is a specialized organic compound featuring a thienyl group and a hydroxyketone moiety. This unique structure grants it versatile applications in pharmaceuticals, agrochemicals, and material science. With the rising demand for heterocyclic compounds in drug discovery, this molecule has garnered significant attention for its potential as a building block in synthetic chemistry. Researchers and manufacturers alike are exploring its role in green chemistry and sustainable synthesis, aligning with global trends toward eco-friendly production methods.

The compound’s molecular formula and structural features make it a candidate for catalysis and ligand design. Recent studies highlight its utility in metal-organic frameworks (MOFs) and polymer modification, addressing key challenges in energy storage and biodegradable materials. As industries prioritize circular economy principles, Ethanone, 2-hydroxy-1-(2-thienyl)- is being evaluated for its recyclability and low environmental impact.

In the pharmaceutical sector, this compound’s bioactive potential is under scrutiny. Its thiophene ring is known to enhance drug bioavailability, making it valuable for API intermediates. Questions like "How does 2-hydroxy-1-(2-thienyl) ethanone interact with enzymes?" or "What are its derivatives in anticancer research?" reflect growing interest in its mechanistic pathways. Analytical techniques such as HPLC and NMR spectroscopy are routinely employed to characterize its purity and stability.

From an industrial perspective, CAS No. 88511-88-0 is often discussed alongside cost-effective synthesis routes and scalability. Innovations in continuous flow chemistry have reduced production waste, while machine learning models optimize reaction conditions. These advancements address frequent queries like "How to improve yield in 2-thienyl hydroxyketone synthesis?"—a testament to its commercial relevance.

Regulatory compliance remains critical. While not classified as hazardous, proper storage conditions (e.g., inert atmospheres) and handling protocols are emphasized to maintain integrity. The compound’s safety data sheets (SDS) provide detailed guidance, ensuring adherence to REACH and FDA guidelines.

Looking ahead, Ethanone, 2-hydroxy-1-(2-thienyl)- is poised to play a pivotal role in smart materials and personalized medicine. Its integration with nanotechnology and 3D printing exemplifies cross-disciplinary innovation. As researchers decode its full potential, this compound will continue to bridge gaps between academia and industry, answering pressing questions in modern chemistry.

• 88-15-3(2-Acetylthiophene)
• 704-38-1(Bis(2-thienyl) ketone)
• 207735-99-7(Ethenone,2-hydroxy-2-(2-thienyl)-)
• 13679-74-8(2-Acetyl-5-methylthiophene)
• 18761-46-1(1-(5-ethylthien-2-yl)ethanone)
• 102499-76-3(Copper, diaquabis(a-oxo-2-thiopheneacetato)-,(OC-6-12)- (9CI))
• 97511-16-5(1-(2-Thienyl)-ethanone)
• 4075-59-6(α-oxo-2-Thiopheneacetic Acid)
• 138380-43-5(2,2-Dihydroxy-1-(thiophen-2-yl)ethanone)
• 127256-00-2(Ethanone,2,2-dimethoxy-1-(2-thienyl)-)