• 1. Enabling stable MnO2 matrix for aqueous zinc-ion battery cathodes?
  Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
• 2. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 3. Exchanged ligands on the surface of a giant cluster: [(MoO3)176(H2O)63(CH3OH)17Hn](32 – n)–
  Chem. Commun., 1998, 1501-1502
• 4. Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe?
  Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
• 5. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198

• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Aryl halides Aryl bromides

Comprehensive Guide to 4-Bromo-2-(diethoxymethyl)thiophene (CAS No. 1487-22-5): Properties, Applications, and Market Insights

4-Bromo-2-(diethoxymethyl)thiophene (CAS No. 1487-22-5) is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, agrochemicals, and material science. This brominated thiophene derivative is characterized by its unique molecular structure, which includes a diethoxymethyl group and a bromo substituent. These functional groups make it a versatile intermediate in synthetic chemistry, particularly in the development of advanced materials and bioactive molecules.

The growing interest in 4-bromo-2-(diethoxymethyl)thiophene is driven by its potential applications in organic electronics and drug discovery. Researchers are increasingly exploring its role in the synthesis of conductive polymers and small-molecule pharmaceuticals, aligning with the global push toward sustainable and high-performance materials. Its CAS number 1487-22-5 is frequently searched in scientific databases, reflecting its relevance in cutting-edge research.

One of the most notable properties of 4-bromo-2-(diethoxymethyl)thiophene is its stability under various reaction conditions, making it a reliable building block for complex chemical transformations. The thiophene ring in its structure is particularly valuable for designing π-conjugated systems, which are essential for applications in OLEDs (organic light-emitting diodes) and solar cells. This aligns with the current industry focus on renewable energy and eco-friendly technologies.

In the pharmaceutical sector, 4-bromo-2-(diethoxymethyl)thiophene is often utilized as a precursor for the synthesis of heterocyclic compounds with potential therapeutic effects. Its bromo group allows for further functionalization, enabling the creation of targeted molecules for drug development. This has led to increased demand for CAS 1487-22-5 in research laboratories and pharmaceutical manufacturing.

Market trends indicate a rising demand for brominated thiophene derivatives, driven by advancements in material science and medicinal chemistry. The compound’s compatibility with cross-coupling reactions and other modern synthetic techniques further enhances its appeal. As industries prioritize innovation, 4-bromo-2-(diethoxymethyl)thiophene is poised to play a pivotal role in the development of next-generation technologies.

For researchers and manufacturers, understanding the safety and handling of 4-bromo-2-(diethoxymethyl)thiophene is crucial. While it is not classified as a hazardous material, standard laboratory precautions should be followed to ensure safe usage. Proper storage conditions and handling protocols are recommended to maintain its stability and efficacy in various applications.

In summary, 4-bromo-2-(diethoxymethyl)thiophene (CAS No. 1487-22-5) is a multifaceted compound with significant potential across multiple industries. Its unique chemical properties, coupled with its applicability in high-tech materials and pharmaceuticals, make it a valuable asset for researchers and businesses alike. As the scientific community continues to explore its capabilities, this compound is expected to remain at the forefront of 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)