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Dec . 11, 2024 19:48 Back to list

4-fluoro-3-methylphenol cas 452-70-0



4-Fluoro-3-Methylphenol A Comprehensive Overview


Introduction


4-Fluoro-3-methylphenol, with the chemical structure C7H7F O, is a significant compound in organic chemistry. Its CAS (Chemical Abstracts Service) number 452-70-0 identifies it within a vast library of chemical substances. This compound consists of a phenolic ring substituted with both a fluorine atom and a methyl group, making it a unique member of the phenol family. The compound is recognized for its various applications in different fields, particularly in pharmaceuticals and agrochemicals.


Chemical Properties

4-Fluoro-3-methylphenol is characterized by its molecular formula, which conveys important information about its composition. The presence of the hydroxyl (-OH) group makes it a phenol, giving it acidic properties. The fluorine atom is an electronegative substituent, which influences the compound's reactivity and biological properties. The compound has a molecular weight of approximately 140.14 g/mol, and its melting point is around 44-46 °C. It is soluble in organic solvents, although it presents lower solubility in water, which is typical for many phenolic compounds.


Synthesis


Several methods exist for the synthesis of 4-fluoro-3-methylphenol, with varying pathways depending on the desired purity and yield. One common synthesis route involves starting with 3-methylphenol and introducing fluorine through electrophilic aromatic substitution. This method requires careful control of reaction conditions, such as temperature and the presence of catalysts, to ensure selective fluorination at the 4-position. Other methods may utilize different precursors or reagents, depending on laboratory capabilities and desired outcomes.


4-fluoro-3-methylphenol cas 452-70-0

4-fluoro-3-methylphenol cas 452-70-0

Applications


4-Fluoro-3-methylphenol finds numerous applications across various fields. As a phenolic compound, it serves as an intermediate in the synthesis of more complex molecules in agrochemicals and pharmaceuticals. It can be used to produce fungicides and insecticides, contributing significantly to agricultural chemistry. The unique properties imparted by the fluorine and methyl groups can enhance the efficacy of these agrochemical products.


In the pharmaceutical sector, 4-fluoro-3-methylphenol can be a precursor in the synthesis of several therapeutic agents. Its role as a starting material in drug formulation is beneficial due to its reactivity and the potential to modify its structure for improved bioactivity. Notably, the introduction of fluorine into drug candidates often improves metabolic stability, making them more effective in therapeutic applications.


Safety and Handling


As with many chemical compounds, proper safety measures are crucial when handling 4-fluoro-3-methylphenol. The compound should be stored in a cool, dry place, away from incompatible substances, and handled in a well-ventilated area or fume hood. Although specific safety data sheets (SDS) provide in-depth information on toxicity and handling precautions, it is generally advised to minimize exposure, use personal protective equipment, and implement safe disposal practices for any waste generated during its use.


Conclusion


In summary, 4-Fluoro-3-methylphenol is a compound with significant utility in various scientific domains. Its unique chemical properties derived from its structure render it valuable in both agrochemical and pharmaceutical applications. As research continues to uncover new aspects of this compound, its relevance in synthetic chemistry is likely to expand further. Offering new pathways for drug and agrochemical development, 4-fluoro-3-methylphenol stands out as a noteworthy compound in contemporary chemistry.


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