• 1. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 2. Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction?
  Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
• 3. 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
• 4. 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
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  Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651

• Solvents and Organic Chemicals Organic Compounds Benzenoids Anthracenes Anthraquinones
• Anthraquinones

Comprehensive Overview of 9,10-Dioxo-9,10-dihydroanthracene-2-carbaldehyde (CAS No. 6363-86-6)

9,10-Dioxo-9,10-dihydroanthracene-2-carbaldehyde (CAS No. 6363-86-6) is a highly specialized organic compound with significant applications in the fields of dye synthesis, pharmaceutical intermediates, and advanced material research. This compound, characterized by its distinctive anthraquinone backbone and aldehyde functional group, has garnered attention for its unique chemical properties and versatility in industrial and academic settings. Researchers and manufacturers are increasingly exploring its potential in sustainable chemistry and green synthesis, aligning with global trends toward eco-friendly production methods.

The molecular structure of 9,10-dioxo-9,10-dihydroanthracene-2-carbaldehyde features a conjugated system that contributes to its stability and reactivity. This makes it a valuable precursor for synthesizing high-performance dyes and functional materials. Recent studies highlight its role in developing organic semiconductors and photocatalysts, addressing growing demand in renewable energy technologies. Its aldehyde group also enables facile derivatization, opening doors to customized chemical modifications for targeted applications.

In the context of user search trends, queries such as "anthraquinone derivatives applications" and "sustainable dye intermediates" reflect rising interest in this compound’s industrial relevance. Additionally, questions like "how to synthesize 9,10-dioxo-9,10-dihydroanthracene-2-carbaldehyde" or "safety data for CAS 6363-86-6" indicate a need for technical and practical information. Addressing these, this article emphasizes the compound’s synthesis routes—often involving oxidation of anthracene derivatives—and its handling under standard laboratory protocols.

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Quality control and analytical methods for 9,10-dioxo-9,10-dihydroanthracene-2-carbaldehyde typically involve HPLC, NMR spectroscopy, and mass spectrometry. These techniques ensure purity and consistency, critical for research and commercial use. As regulatory frameworks evolve, compliance with REACH and other international standards remains a priority for suppliers and end-users alike.

In summary, 9,10-Dioxo-9,10-dihydroanthracene-2-carbaldehyde (CAS No. 6363-86-6) stands at the intersection of innovation and sustainability. Its multifaceted applications, coupled with increasing demand for specialty chemicals, position it as a compound of enduring scientific and industrial interest. Future research may unlock further potentials in smart materials and green chemistry, solidifying its role in next-generation technologies.

• 954-16-5(2,4,6-Trimethylbenzophenone)
• 89-74-7(2',4'-Dimethylacetophenone)
• 3029-32-1(6,13-Pentacenequinone)
• 82-05-3(1,9-Benz-10-anthrone)
• 84-65-1(Anthraquinone)
• 577-16-2(2'-Methylacetophenone)
• 84-47-9(2-Tert-Butylanthraquinone)
• 84-51-5(2-Ethylanthraquinone)
• 131-58-8(2-Methylbenzophenone)
• 84-54-8(2-Methylanthraquinone)