Sodium iopanoate

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Identification

Molecular formula
C11H12I3NNaO3
CAS Number
338-05-0
IUPAC Name
sodium;2-[[2,4,6-triiodo-3-(2-oxopyrrolidin-1-yl)phenyl]methyl]butanoate
Molecular Weight
821.92g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
2.1000g/cm3
Interesting facts

Exploring 2-[[2,4,6-triiodo-3-(2-oxopyrrolidin-1-yl)phenyl]methyl]butanoate

2-[[2,4,6-triiodo-3-(2-oxopyrrolidin-1-yl)phenyl]methyl]butanoate presents a fascinating study in the realm of organic chemistry, especially regarding halogenated compounds and their applications. Here are some interesting facts about this compound:

  • Structure and Function: The compound features a unique arrangement of a butanoate group tethered to a highly substituted aromatic ring containing iodine atoms. The presence of the iodine atoms significantly enhances its reactivity and makes it a subject of interest for synthesis.
  • Biological Significance: Compounds like this one are often investigated for their potential applications in medicinal chemistry. The oxopyrrolidine moiety may contribute to biological activity, making it relevant in drug design.
  • Halogen Chemistry: The incorporation of iodine into organic molecules can impart unique properties such as increased lipophilicity and altered optical characteristics. Interestingly, iodine's high atomic number often results in enhanced X-ray attenuation, making these compounds useful in imaging applications.
  • Reactivity: The halogens, particularly iodine, can participate in further chemical reactions, allowing for the synthesis of even more complex molecules through substitution and coupling reactions.

As researchers continue to unpack the potential uses of 2-[[2,4,6-triiodo-3-(2-oxopyrrolidin-1-yl)phenyl]methyl]butanoate, the implications for pharmaceuticals and materials science are endless. Its intricate structure serves as a reminder of the creativity inherent in organic synthesis, urging us to explore how such compounds can solve real-world challenges.

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