Ioversol

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Identification

Molecular formula
C18H24I3N3O9
CAS Number
87771-40-2
IUPAC Name
2-phenyl-2-[2,4,6-triiodo-3-(2-oxomorpholin-4-yl)phenoxy]acetic acid
Molecular Weight
807.11g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4690g/cm3
Interesting facts

Interesting Facts About 2-Phenyl-2-[2,4,6-triiodo-3-(2-oxomorpholin-4-yl)phenoxy]acetic Acid

The compound known as 2-phenyl-2-[2,4,6-triiodo-3-(2-oxomorpholin-4-yl)phenoxy]acetic acid is a fascinating example in the realm of organic chemistry, particularly due to its unique molecular structure and potential applications.

Structural Insights

  • Aromatic Character: This compound features a phenyl group attached to a phenoxy moiety, which results in significant aromatic stability.
  • Halogenation: The presence of multiple iodine substituents (triiodo) can greatly influence the compound's reactivity and by extension, its biological activity.
  • Morpholine Derivative: The inclusion of the morpholine ring suggests the potential for pharmacological applications, as many drugs utilize morpholinic structures to enhance solubility and binding properties.

Biological Significance

Research indicates that compounds with such halogen substitutions often show enhanced biological activities. For instance, they can exhibit:

  • Antimicrobial Activity: Halogenated organic compounds are frequently analyzed for their effects against various bacterial strains.
  • Anticancer Properties: Compounds with complex structures like this one are sometimes investigated for their ability to inhibit cancer cell proliferation.
  • Analgesic Effects: Thanks to their structural groups, these compounds may interact with pain receptors, providing potential for pain relief studies.

Synthesis Challenges

The synthesis of such a complex molecule typically involves intricate synthetic routes that can include:

  • Multi-step reactions that may require careful optimization.
  • The need for regioselective halogenation - a challenging aspect of organic synthesis.
  • Handling of toxic reagents typically associated with halogenation processes.

As one scientist quipped, "The beauty of organic chemistry lies in its complexity, where every bond tells a story." This compound is a prime illustration of that sentiment, embodying the intricate dance between structure, reactivity, and biological significance.

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