• 1. Studies related to anthracyclines. Part 1. Some Diels–Alder reactions of 4a,9a-epoxy-4a,9a-dihydroanthracene-1,4,9,10-tetrone
  Malcolm Chandler,Richard J. Stoodley J. Chem. Soc. Perkin Trans. 1 1980 1007

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

Anthracenetetrone (CAS No. 1709-63-3): A Comprehensive Overview

Anthracenetetrone, also known by its CAS registry number CAS No. 1709-63-3, is a highly intriguing compound that has garnered significant attention in the fields of organic chemistry, materials science, and pharmacology. This compound, which belongs to the class of anthraquinones, is characterized by its unique molecular structure and versatile applications. In recent years, advancements in synthetic methodologies and computational modeling have shed new light on its properties and potential uses.

The molecular structure of Anthracenetetrone comprises an anthracene backbone with four ketone groups strategically positioned at the 1,4,9, and 10 positions. This arrangement not only imparts the compound with a high degree of conjugation but also confers it with unique electronic properties. Researchers have exploited these properties to develop novel materials for optoelectronic devices, such as organic light-emitting diodes (OLEDs) and photovoltaic cells. Recent studies have demonstrated that Anthracenetetrone-based materials exhibit enhanced charge transport characteristics, making them promising candidates for next-generation electronic devices.

One of the most significant breakthroughs in the study of Anthracenetetrone has been the development of efficient synthetic routes. Traditionally, the synthesis of anthraquinones involved multi-step processes that often required harsh reaction conditions. However, recent advancements in catalytic chemistry have enabled the production of Anthracenetetrone through more sustainable and cost-effective methods. For instance, researchers have successfully utilized transition metal catalysts to achieve high yields of the compound under mild conditions. These developments not only enhance the scalability of production but also align with current trends toward green chemistry.

In addition to its role in materials science, Anthracenetetrone has also emerged as a valuable tool in drug discovery. The compound's ability to interact with biological systems has been extensively studied, particularly in the context of its potential as an anti-cancer agent. Recent research has shown that Anthracenetetrone exhibits selective cytotoxicity against cancer cells while sparing healthy cells. This property makes it a compelling candidate for further preclinical studies aimed at developing novel anti-cancer therapies.

The versatility of Anthracenetetrone extends to its applications in sensing technologies. Due to its high sensitivity to environmental changes, such as pH and temperature fluctuations, the compound has been integrated into sensors for detecting various analytes. For example, researchers have developed a Anthracenetetrone-based sensor capable of detecting heavy metal ions in water samples with unprecedented accuracy. Such innovations underscore the compound's potential in environmental monitoring and public health applications.

The growing interest in CAS No. 1709-63-3 can also be attributed to its role as a building block in supramolecular chemistry. By incorporating Anthracenetetrone into self-assembling systems, scientists have created nanostructured materials with tailored functionalities. These materials hold promise for applications ranging from drug delivery systems to catalysis.

In conclusion, Anthracenetetrone (CAS No. 1709-63-3) stands as a testament to the boundless creativity and ingenuity of modern chemistry. Its unique properties and diverse applications continue to inspire researchers across disciplines. As our understanding of this compound deepens through ongoing research efforts, it is likely that new breakthroughs will emerge that further expand its utility in both academic and industrial settings.

• 2124-57-4(Menaquinone-7)
• 27670-93-5(Menaquinone 12)
• 84-81-1(Menaquinone 6)
• 11032-49-8(vitamin K2)
• 27123-36-0(Menaquinone 13)
• 1182-68-9(Menaquinone 5)
• 84-80-0(Vitamin K1)
• 523-39-7(Menaquinone 9)
• 863-61-6(Menaquinone 4(Mixture of cis-trans isomers))
• 12001-79-5(Vitamin K)