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  Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
• 2. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoyl derivatives
• Other Chemical Reagents Derivatization Reagents
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Comprehensive Guide to (4-Formyl-2-methoxyphenyl)boronic acid (CAS No. 1028479-47-1): Properties, Applications, and Market Insights

(4-Formyl-2-methoxyphenyl)boronic acid (CAS No. 1028479-47-1) is a specialized boronic acid derivative widely used in organic synthesis, pharmaceutical research, and material science. This compound, featuring both a formyl group and a methoxy group on its phenyl ring, is valued for its versatility in Suzuki-Miyaura cross-coupling reactions, a cornerstone of modern synthetic chemistry. Researchers and industries frequently search for "boronic acid applications" or "CAS 1028479-47-1 supplier," highlighting its growing relevance in drug discovery and advanced material development.

The molecular structure of (4-Formyl-2-methoxyphenyl)boronic acid enables its role as a key intermediate in synthesizing complex molecules. Its boron-containing functional group facilitates the formation of carbon-carbon bonds, making it indispensable for creating biaryl compounds used in OLEDs, liquid crystals, and bioactive molecules. Recent trends in "green chemistry" and "sustainable synthesis" have further amplified interest in this compound, as it often reduces the need for toxic catalysts in coupling reactions.

In pharmaceutical applications, 1028479-47-1 serves as a building block for protease inhibitors and kinase-targeted drugs, aligning with the surge in searches for "boronic acid in drug design." Its unique electronic properties, influenced by the methoxy substituent, enhance binding affinity in drug-receptor interactions. Laboratories optimizing "high-throughput screening" protocols also prioritize this compound due to its stability and compatibility with automated synthesis platforms.

The global market for (4-Formyl-2-methoxyphenyl)boronic acid reflects its expanding applications, with suppliers emphasizing "high-purity boronic acids" for research-grade and industrial-scale use. Analytical techniques like HPLC and NMR ensure quality control, addressing frequent queries about "CAS 1028479-47-1 characterization." Storage recommendations typically suggest anhydrous conditions to preserve its reactivity, a detail often sought in "boronic acid handling guidelines."

Emerging studies explore its utility in covalent organic frameworks (COFs) and sensor materials, responding to trending searches like "boronic acid sensors for glucose detection." As industries seek alternatives to conventional materials, this compound’s role in smart coatings and molecular electronics continues to gain traction. Regulatory-compliant synthesis methods (e.g., REACH) further bolster its adoption in European and North American markets.

For researchers investigating "structure-activity relationships," the formyl group in 1028479-47-1 offers a handle for further derivatization, enabling tailored modifications. This adaptability aligns with the demand for "custom boronic acid derivatives" in academic and industrial settings. Recent patents highlight its use in photocatalysis and metal-organic frameworks (MOFs), areas generating significant scientific interest.

In summary, (4-Formyl-2-methoxyphenyl)boronic acid (CAS No. 1028479-47-1) bridges multiple disciplines, from medicinal chemistry to advanced materials. Its synergy with cutting-edge research themes—such as "click chemistry" and "precise molecular editing"—ensures its enduring relevance. Suppliers and researchers alike benefit from understanding its multifaceted applications, quality benchmarks, and evolving market dynamics.

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