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• 2. Exchangeability of amino acid residues with similar physicochemical properties in coiled-coil interactions?
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• 4. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes Naphthalenes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Naphthalenes
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Professional Introduction to 2-Iodonaphthalene (CAS No. 612-55-5)

2-Iodonaphthalene, with the chemical name 2-Iodobenzene, is a significant compound in the field of organic synthesis and pharmaceutical research. Its molecular formula, C₁₀H₆I, underscores its role as an important intermediate in various chemical transformations. This compound, identified by the CAS number CAS No. 612-55-5, has garnered considerable attention due to its versatile applications in medicinal chemistry and material science.

The structural integrity of 2-Iodonaphthalene, featuring a naphthalene core substituted with an iodine atom at the 2-position, makes it a valuable reagent in cross-coupling reactions. These reactions are pivotal in constructing complex molecular architectures, which are often essential in the development of novel therapeutic agents. The iodine atom's presence facilitates its participation in palladium-catalyzed reactions, such as Suzuki-Miyaura and Stille couplings, enabling the formation of carbon-carbon bonds that are crucial for drug design.

In recent years, 2-Iodonaphthalene has been extensively studied for its potential in pharmaceutical applications. Researchers have leveraged its reactivity to develop new synthetic pathways for bioactive molecules. For instance, its use in the synthesis of antiviral and anticancer agents has shown promising results. The compound's ability to undergo selective functionalization has allowed chemists to tailor its structure for specific biological targets, enhancing its utility in drug discovery.

The compound's role extends beyond pharmaceuticals into the realm of materials science. Its incorporation into organic electronic materials has led to advancements in optoelectronic devices. The iodine substituent influences the electronic properties of naphthalene derivatives, making them suitable for applications in organic light-emitting diodes (OLEDs) and photovoltaic cells. This intersection of chemistry and technology highlights the multifaceted nature of 2-Iodonaphthalene.

Recent studies have also explored the environmental and toxicological aspects of 2-Iodonaphthalene. While it is not classified as a hazardous material, understanding its behavior under various conditions is essential for safe handling and disposal. Researchers are investigating its degradation pathways and potential impacts on ecosystems, ensuring that its use aligns with sustainable practices.

The industrial production of 2-Iodonaphthalene involves well-established synthetic routes that ensure high purity and yield. Manufacturers adhere to stringent quality control measures to meet the demands of both academic and industrial research sectors. The compound's commercial availability makes it accessible for a wide range of applications, fostering innovation across multiple disciplines.

Looking ahead, the future prospects of 2-Iodonaphthalene are bright, with ongoing research uncovering new possibilities for its use. Advances in synthetic methodologies and computational chemistry are expected to further enhance its utility in drug development and material science. As our understanding of molecular interactions deepens, compounds like 2-Iodonaphthalene will continue to play a pivotal role in advancing scientific knowledge and technological innovation.

• 17024-12-3(9-Iodophenanthrene)
• 58556-77-7(Naphthalene, 2,7-diiodo-)
• 62607-37-8(1-Naphthalenyl, 5-iodo-)
• 62325-31-9(Phenanthrene, 2,7-diiodo-)
• 22362-86-3(9-Iodoanthracene)
• 33240-31-2(3-Iodophenanthrene)
• 90-14-2(1-Iodonaphthalene)
• 55691-84-4(2-Iodophenanthrene)
• 113705-11-6(Anthracene, 9,10-diiodo-)
• 27715-44-2(1,5-Diiodonaphthalene)