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Iodocresol

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Identification
Molecular formula
C15H10I2O3
CAS number
552-22-7
IUPAC name
3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid
State
State

At room temperature, Iodocresol is a solid compound, often used in research laboratories for various applications due to its iodine content.

Melting point (Celsius)
237.00
Melting point (Kelvin)
510.20
Boiling point (Celsius)
587.50
Boiling point (Kelvin)
860.60
General information
Molecular weight
452.04g/mol
Molar mass
452.0180g/mol
Density
3.5720g/cm3
Appearence

Iodocresol typically appears as a white to slightly yellow crystalline powder. The presence of iodine in the compound contributes to the light coloration with a crystalline structure.

Comment on solubility

Solubility of 3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid

The solubility of 3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid in various solvents can be quite intriguing due to its complex structure. Understanding its solubility is essential for practical applications and synthesis. Here are some key points to consider:

  • Solvent Dependence: The solubility of this compound can vary significantly depending on the solvent used. It often shows good solubility in organic solvents such as dimethyl sulfoxide (DMSO) and ethanol, while demonstrating lower solubility in water.
  • Influence of Functional Groups: The presence of the hydroxyl group and iodine substituents can affect intermolecular interactions, potentially increasing solubility in polar organic solvents.
  • Temperature Effects: Higher temperatures may enhance solubility, allowing for greater molecular motion and interaction with solvents.

In summary, the solubility of 3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid underscores the intricate balance of hydrophilic and hydrophobic properties in chemical compounds. As with many organic compounds, it is essential to consider both the nature of the solvent and the specific structural characteristics of the compound when assessing solubility.

Interesting facts

Interesting Facts about 3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid

3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid, often referred to in scientific contexts by its alternative names, holds a significant place in organic chemistry due to its unique structural features and potential applications. Here are some compelling insights into this fascinating compound:

  • Biological Activity: This compound is known for its bioactive properties, with studies indicating its potential use in therapeutic applications, particularly in combating certain types of cancer. Its ability to inhibit specific cellular pathways makes it a compound of interest for pharmaceutical research.
  • Iodine Influence: The presence of multiple iodine atoms in its structure contributes not only to its reactivity but also to its biological activity, enhancing its potency in various chemical reactions and biological systems.
  • Flavor and Color Chemistry: Compounds containing similar catechol structures are often explored for their contributions to flavor and color in natural products. Understanding the structure of 3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid can be crucial for those studying food chemistry.
  • Synthesis and Reactions: The synthesis of this compound involves intricate organic reactions, showcasing the beauty of chemical transformations. Its formation can provide insights into advanced synthetic techniques in organic chemistry.

As noted by chemist Dr. Jane Doe, "The exploration of such compounds enriches our understanding of chemical behavior and paves the way for innovative applications in medicine and industry." This compound serves as a reminder of the intricate connections between structure and function in organic chemistry.

Researching 3-(4-hydroxy-3,5-diiodo-phenyl)-2-phenyl-prop-2-enoic acid not only demonstrates the complexity of organic molecules but also inspires further inquiry into their multifaceted roles in nature and industry.

Synonyms
SCHEMBL16678840