Iohexol

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Identification

Molecular formula
C19H26I3N3O9
CAS Number
66108-95-0
IUPAC Name
3-acetamido-5-(2-hydroxyethylcarbamoyl)-2,4,6-triiodo-benzoic acid;6-(methylamino)hexane-1,2,3,4,5-pentol
Molecular Weight
821.14g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4000g/cm3
Synonyms
3-[(1-Hydroxyethylidene)amino]-5-{hydroxy[(2-hydroxyethyl)imino]methyl}-2, 4, 6-triiodobenzoic acid--1-deoxy-1-(methylamino)hexitol (1/1)
Interesting facts

Exploring 3-Acetamido-5-(2-hydroxyethylcarbamoyl)-2,4,6-triiodo-benzoic Acid

This fascinating compound is known for its unique structural features and potential applications in various scientific fields. Here are some interesting facts about it:

  • Health Applications: The presence of iodine in its structure makes it a compound of interest in medical imaging, notably in X-ray contrast agents, as iodine can enhance contrast in imaging techniques.
  • Biological Activity: Its acetamido and hydroxyethylcarbamoyl groups suggest that this compound may exhibit biological activities, potentially being studied for pharmaceutical applications such as drug formulation.
  • Novel Synthesis: Chemists are continually exploring synthetic pathways to create such compounds, incorporating different functional groups to enhance efficacy and reduce toxicity.

"Chemistry is the building block of life," and compounds like this one exemplify how specific molecular configurations can lead to significant practical applications.

Exploring 6-(Methylamino)hexane-1,2,3,4,5-pentol

This compound is characterized by its complex polyol structure, offering a range of chemical properties and potential applications. Below are some key points of interest:

  • Polyol Characteristics: The presence of multiple hydroxyl (-OH) groups contributes to the compound's potential use in the development of biodegradable polymers and drug delivery systems.
  • Biochemical Relevance: Its methylamino group can enhance the solubility and bioavailability of drugs, making it relevant in medicinal chemistry.
  • Versatile Reactions: The hydroxyl groups allow for numerous derivatization reactions, giving chemists flexibility in modifying the compound for specific applications.

In the world of chemical science, these intricate compounds serve as a reminder of the complexity and beauty of molecular interactions. Understanding and manipulating these structures can lead to groundbreaking innovations in medicine and technology.

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