Iopanoic acid
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- Molecular formula
- C11H12I3NO2
- CAS Number
- 96-83-3
- IUPAC Name
- 2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid
- Molecular Weight
- 597.88g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.7800g/cm3
- Appearance
- depending on its purity and the presence of any impurities, but it is generally recognized by its powder form in laboratory and pharmaceutical settings.
- Synonyms
- 21762-25-4
Identification
Interesting facts
Interesting Facts about 2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid
2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid, often referred to for its intriguing chemical structure and diverse applications, is noteworthy for several reasons:
- Biological Significance: This compound has shown potential as a pharmaceutical intermediate. Its unique functional groups allow it to interact effectively with various biological pathways, making it a candidate in drug development.
- X-ray Contrast Agent: The presence of tri-iodo substitutions in the phenyl ring endows this compound with vibrant X-ray attenuation properties. As such, it can play a crucial role in medical imaging, particularly in enhancing the visibility of structures in the body during diagnostic procedures.
- Environmental Considerations: Due to its iodine content, the environmental impact of this compound is an essential factor for researchers and chemists. Understanding its degradation pathways and potential bioaccumulation in the environment is key for sustainable usage.
- Research Applications: Chemists engage this compound in studies related to organic synthesis and medicinal chemistry, examining its structure-activity relationship (SAR) which can illuminate how variations in structure influence its biological efficacy.
- Versatile Synthesis: The synthesis of this compound often involves multi-step organic reactions, showcasing the creative ingenuity of chemists. From amino acid precursors to halogenation processes, the pathways leading to its formulation are complex and fascinating.
In summary, 2-(3-amino-2,4,6-triiodo-phenyl)butanoic acid serves as a reminder of the intricate relationship between chemical structure and application. Its properties not only make it a significant candidate in medicinal chemistry but also underline the implications of chemical science in both healthcare and environmental stewardship.