(4-Iodophenyl)methanol

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Identification

Molecular formula
C7H7IO
CAS Number
2822-58-8
IUPAC Name
(4-iodophenyl)methanol
Molecular Weight
234.04g/mol
Melting Point
which keeps it in the solid state under normal environmental conditions.
Boiling Point
(Celsius)
Density
2.1826g/cm3
Synonyms
4-Iodobenzyl alcohol
Interesting facts

Interesting Facts about (4-Iodophenyl)methanol

(4-Iodophenyl)methanol is a fascinating compound that belongs to the class of organic compounds known as aryl alcohols. Its unique structure, featuring an iodine atom attached to a benzene ring, allows for a range of intriguing properties and potential applications.

Key Characteristics

  • Functional Groups: The presence of both a hydroxyl group (-OH) and an aryl group makes (4-iodophenyl)methanol a significant candidate in the field of organic synthesis.
  • Reactivity: The iodine atom enhances the electrophilic character of the aromatic ring, facilitating various chemical reactions, such as nucleophilic substitution.
  • Applications: This compound is not only used as an intermediate in the synthesis of pharmaceuticals but also in the development of agrochemicals.

Scientific Significance

Research indicates that compounds like (4-iodophenyl)methanol can exhibit biological activity, making them potentially valuable in medicinal chemistry. For example:

  • Studies have shown that related compounds can possess antibacterial and antifungal properties.
  • The ability to modify the structure of (4-iodophenyl)methanol allows for the exploration of a diverse range of derivatives with varying biological activities.

As a chemistry student or scientist, exploring the reactivity and potential applications of (4-iodophenyl)methanol opens up exciting avenues for research, especially in the context of creating novel compounds that address emerging health challenges.

Conclusion

In summary, (4-iodophenyl)methanol is a compound rich in possibilities, blending the interplay of organic chemistry with potential real-world applications. Its unique features render it a compelling subject of study, paving the way for future innovations in both chemical synthesis and pharmaceutical development.

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