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  Hyejin Moon,Aaron R. Wheeler,Robin L. Garrell,Chang-Jin “CJ” Kim Lab Chip, 2006,6, 1213-1219
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  Adeline Huiling Loo,Alessandra Bonanni,Martin Pumera Analyst, 2013,138, 467-471
• 3. Alternative donor substrates for inverting and retaining glycosyltransferases?
  Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367
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  Philipp Traber,Stephan Kupfer,Stefanie Gr?fe,Isabelle Baussanne,Martine Demeunynck,Jean-Marie Mouesca,Serge Gambarelli,Vincent Artero,Murielle Chavarot-Kerlidou Chem. Sci., 2018,9, 4152-4159

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Benzofurans Dibenzofurans

Dibenzofuran-1-ol: A Comprehensive Overview

Dibenzofuran-1-ol, also known by its CAS number 33483-06-6, is a fascinating compound that has garnered significant attention in the fields of organic chemistry and materials science. This compound, with the molecular formula C₁₄H₁₀O, belongs to the class of dibenzofurans, which are polycyclic aromatic compounds with a furan ring fused to two benzene rings. The dibenzofuran structure is notable for its rigid and planar geometry, which contributes to its unique electronic properties.

The dibenzofuran framework has been extensively studied due to its potential applications in optoelectronic devices, such as organic light-emitting diodes (OLEDs) and photovoltaic cells. Recent research has focused on modifying the dibenzofuran core to enhance its electronic properties, making it more suitable for these applications. For instance, the introduction of electron-donating or withdrawing groups can significantly alter the compound's absorption and emission spectra, which are critical parameters for OLED performance.

In addition to its electronic properties, dibenzofuran derivatives have shown promise in the field of drug discovery. The compound's ability to interact with biological systems has led researchers to explore its potential as a scaffold for new pharmaceutical agents. For example, studies have demonstrated that certain dibenzofuran derivatives exhibit anti-inflammatory and antioxidant activities, making them valuable candidates for further investigation in medicinal chemistry.

The synthesis of dibenzofuran derivatives has also been a topic of interest in recent years. Traditional methods often involve complex multi-step reactions, but advancements in catalytic chemistry have enabled more efficient and selective syntheses. For instance, the use of transition metal catalysts has facilitated the construction of the dibenzofuran framework through cross-coupling reactions. These developments have not only simplified the synthesis process but also opened up new avenues for functionalizing the molecule with various substituents.

From an environmental perspective, understanding the fate and behavior of dibenzofuran compounds in natural systems is crucial. Recent studies have examined the degradation pathways of these compounds under various environmental conditions, such as sunlight exposure and microbial activity. These investigations are essential for assessing their potential impact on ecosystems and guiding their safe use in industrial applications.

In conclusion, dibenzofuran derivatives like Dibenzofuran-1-ol continue to be a subject of intense research due to their versatile properties and wide-ranging applications. As advancements in synthetic methodologies and material science continue to unfold, it is likely that this compound will play an even more significant role in both academic and industrial settings.

• 71878-71-2(2,3-Dibenzofurandiol (7CI,9CI))
• 408338-41-0(5-hydroxy-2,3-dihydro-1-benzofuran-3-one)
• 221652-95-5(1,3,7,9-Tetrahydroxydibenzofuran)
• 82493-21-8(Dibenzofuranol)
• 83025-51-8(Dibenzofuran-1,2-diol)
• 92024-85-6(2,7-Dihydroxydibenzofuran)
• 334970-30-8(1-Dibenzofuranyloxy)
• 480-97-7(1-benzofuran-4-ol)
• 13196-11-7(Benzofuran-6-Ol)
• 20279-16-7(8-oxatricyclo7.4.0.0,2,7trideca-1(9),2(7),3,5,10,12-hexaen-5-ol)