Ioxitalamic acid

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Identification

Molecular formula
C11H9I3NO4
CAS Number
27237-65-4
IUPAC Name
2-(3-acetamido-2,4,6-triiodo-phenoxy)butanoic acid
Molecular Weight
613.97g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
2.1185g/cm3
Synonyms
BRN 2671852
Interesting facts

Interesting Facts about 2-(3-Acetamido-2,4,6-triiodo-phenoxy)butanoic Acid

2-(3-Acetamido-2,4,6-triiodo-phenoxy)butanoic acid is a unique chemical compound that showcases the intricacies of organic chemistry, particularly in the field of pharmaceuticals and medicinal chemistry. Below are some engaging facts about this compound:

  • Composition and Structure: This compound features a triiodo-substituted aromatic ring, which is quite rare in organic compounds. The presence of three iodine atoms significantly influences the compound's chemical behavior and properties.
  • Pharmacological Potential: Due to its structure, this compound has been investigated for its potential applications in drug development related to thyroid disorders and other hormonal treatments. The iodine substituents can mimic the action of naturally occurring iodinated compounds, making it an interesting subject for research.
  • Scientific Interest: The acetamido group in the molecule can enhance its lipophilicity, which is a critical factor in the design of compounds that need to interact with lipid membranes, such as cell membranes.
  • Environmental Considerations: Compounds containing iodine can have implications in environmental chemistry, especially in bioremediation processes and the tracking of chemical transformations in ecosystems.
  • Analytical Techniques: Researchers employ various analytical techniques, such as NMR and mass spectrometry, to characterize and study the behavior of this compound. These methods help elucidate the compound's structure and confirm its purity.

In summary, 2-(3-acetamido-2,4,6-triiodo-phenoxy)butanoic acid not only highlights the depth of synthetic chemistry but also opens avenues for further investigation in both medicinal and environmental applications. The interplay between its iodine substitutions and the butanoic acid moiety presents intriguing possibilities for innovative research.

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