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• 2. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenols Halophenols Fluorophenols
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Comprehensive Guide to 4-Fluoro-2-iodophenol (CAS No. 2713-29-3): Properties, Applications, and Industry Insights

4-Fluoro-2-iodophenol (CAS No. 2713-29-3) is a halogenated phenolic compound gaining traction in pharmaceutical and agrochemical research due to its unique structural properties. As a fluorinated and iodinated derivative of phenol, it serves as a versatile intermediate in organic synthesis. Its molecular formula, C₆H₄FIO, and molecular weight of 238.00 g/mol make it a critical building block for cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig reactions, which are pivotal in drug discovery.

Recent trends in AI-driven drug design and green chemistry have amplified interest in 4-Fluoro-2-iodophenol. Researchers frequently search for "halogenated phenol applications" or "2713-29-3 synthesis methods," reflecting its relevance in optimizing bioactive molecules. The compound’s electron-withdrawing properties enhance reactivity in palladium-catalyzed transformations, a hotspot in medicinal chemistry forums.

From a technical perspective, 4-Fluoro-2-iodophenol exhibits a melting point range of 45–50°C and is typically stored under inert conditions to preserve stability. Its solubility in organic solvents like DMSO and ethanol facilitates its use in high-throughput screening (HTS) workflows. Industry reports highlight its role in developing PET radiotracers, addressing the growing demand for non-invasive diagnostic tools in oncology and neurology.

Environmental and regulatory considerations are also paramount. While not classified as hazardous, its handling requires adherence to REACH and GLP standards. Laboratories prioritize "safe handling of iodophenols" and "2713-29-3 MSDS" queries, underscoring the need for transparent safety data. Innovations in catalytic recycling further align its use with sustainable chemistry goals.

In conclusion, 4-Fluoro-2-iodophenol (CAS No. 2713-29-3) bridges cutting-edge science and industrial practicality. Its applications span drug development, material science, and analytical chemistry, making it a staple in modern R&D. As precision medicine advances, this compound’s role in crafting targeted therapies will only expand, solidifying its niche in the chemical landscape.

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