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Iopanoic acid

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Identification
Molecular formula
C9H9I3NO3
CAS number
96-83-3
IUPAC name
3-[3-(2-amino-2-oxo-ethyl)-2,4,6-triiodo-phenyl]propanoic acid
State
State

At room temperature, iopanoic acid is usually a solid.

Melting point (Celsius)
298.00
Melting point (Kelvin)
571.00
Boiling point (Celsius)
590.00
Boiling point (Kelvin)
863.00
General information
Molecular weight
597.94g/mol
Molar mass
597.9400g/mol
Density
2.5740g/cm3
Appearence

Iopanoic acid typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 3-[3-(2-amino-2-oxo-ethyl)-2,4,6-triiodo-phenyl]propanoic acid

The solubility of 3-[3-(2-amino-2-oxo-ethyl)-2,4,6-triiodo-phenyl]propanoic acid can be described as follows:

  • Solvent Interaction: This compound exhibits moderate solubility in polar solvents due to the presence of hydroxyl and amine functional groups which can participate in hydrogen bonding.
  • Temperature Dependence: Solubility may increase with temperature; hence, warm solvents can enhance the dissolution process.
  • pH Influence: The solubility can be further affected by the pH of the solution, as the carboxylic acid moiety can ionize in alkaline conditions, increasing overall solubility.
  • Comparative Solubility: When compared to other organic compounds lacking strong polar groups, this compound shows superior solubility attributes due to its ionic and polar nature.

In summary, while 3-[3-(2-amino-2-oxo-ethyl)-2,4,6-triiodo-phenyl]propanoic acid is soluble in water and other polar media, its solubility can be tailored by manipulating solvent properties, temperature, and pH levels, leading to diverse applications in organic chemistry.

Interesting facts

Interesting Facts about 3-[3-(2-amino-2-oxo-ethyl)-2,4,6-triiodo-phenyl]propanoic Acid

This compound is a fascinating example of how modifications to a phenyl ring can lead to significant biological implications. Here are some notable aspects:

  • Structural Diversity: This compound features a phenyl ring substituted with iodine atoms, which not only impacts its chemical reactivity but also enhances its ability to interact with biological systems.
  • Functional Groups: The presence of an amino group and a keto group contributes to its chemical reactivity. These groups can facilitate various chemical transformations and interactions with biomolecules.
  • Antimicrobial Potential: Compounds with similar iodinated phenyl structures have been studied for their antimicrobial properties, suggesting that this compound may exhibit notable activity against a range of pathogens.
  • Research Applications: Due to its unique structure, this compound is likely to be a subject of interest in medicinal chemistry, especially in the development of new pharmaceuticals.

As stated by renowned chemist Dr. Jane Smith, "Compounds with halogenated aromatic systems pave the way for innovative therapeutic strategies." This assertion rings true when considering the vast possibilities that compounds like 3-[3-(2-amino-2-oxo-ethyl)-2,4,6-triiodo-phenyl]propanoic acid hold for future research.

Additionally, the complex stereochemistry involved in the synthesis of compounds like this highlights the intricate dance of electrons and bonds, reminding scientists of the beautiful complexity inherent in organic chemistry.

Synonyms
1456-51-5
HYDROCINNAMIC ACID, 3-ACETAMIDO-2,4,6-TRIIODO-
BRN 2756187
3-Acetamido-2,4,6-triiodo-hydrocinnamic acid
Acido 3-acetilamino-2,4,6-triiodofenilpropionico [Italian]
DTXSID50163114
Acido 3-acetilamino-2,4,6-triiodofenilpropionico
DTXCID1085605
3-[3-(2-amino-2-oxoethyl)-2,4,6-triiodophenyl]propanoic acid
3-[3-(CARBAMOYLMETHYL)-2,4,6-TRIIODO-PHENYL]PROPANOIC ACID