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Clorindione

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Identification
Molecular formula
C25H15ClO5
CAS number
338-36-9
IUPAC name
3-[(4-chlorophenyl)-(2-hydroxy-4-oxo-chromen-3-yl)methyl]-2-hydroxy-chromen-4-one
State
State

At room temperature, Clorindione is found in a solid state. Being a crystalline compound, it maintains a defined form and is not readily volatile under standard conditions.

Melting point (Celsius)
225.00
Melting point (Kelvin)
498.15
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.15
General information
Molecular weight
394.84g/mol
Molar mass
394.7900g/mol
Density
1.5079g/cm3
Appearence

Clorindione is a crystalline compound. It typically appears as a solid that can be tan to pale yellow. This appearance is characteristic of many chromenone derivatives, which tend to exhibit a range of pale colors depending on the substituents attached to the chromenone core.

Comment on solubility

Solubility of 3-[(4-chlorophenyl)-(2-hydroxy-4-oxo-chromen-3-yl)methyl]-2-hydroxy-chromen-4-one

The solubility of 3-[(4-chlorophenyl)-(2-hydroxy-4-oxo-chromen-3-yl)methyl]-2-hydroxy-chromen-4-one can be influenced by various factors due to its complex structure. Here are several key considerations:

  • Polarity: The presence of hydroxyl (-OH) groups generally enhances solubility in polar solvents, whereas large hydrophobic groups can decrease it.
  • Hydrogen Bonding: The -OH groups on the compound can engage in hydrogen bonding, potentially increasing solubility in water and other polar solvents.
  • Solvent Interaction: This compound may demonstrate higher solubility in organic solvents like ethanol or methanol compared to water, due to interactions with the aromatic structures.
  • pH Sensitivity: Changes in pH may also affect solubility, especially if there are ionizable groups within the molecular structure.

In summary, the solubility of this compound is likely to vary significantly based on solvent choice and environmental conditions. Experimentation may be necessary to determine the precise solubility in different environments.

Interesting facts

Interesting Facts about 3-[(4-chlorophenyl)-(2-hydroxy-4-oxo-chromen-3-yl)methyl]-2-hydroxy-chromen-4-one

This intriguing compound, known for its complex structure, is a member of the flavonoid family, which boasts a variety of biological activities. Here are some fascinating insights:

  • Flavonoid Derivative: As a flavonoid, this compound contributes to the diverse world of naturally occurring plant pigments. It plays a significant role in various biological and pharmacological interactions.
  • Potential Biological Activities: Research indicates that compounds like this one often exhibit potent antioxidant properties. They may help in combating oxidative stress and could have implications in preventing various diseases.
  • Chlorophenyl Influence: The presence of the 4-chlorophenyl group adds an intriguing aspect, as halogenated compounds are frequently explored for their enhanced biological activity and potency.
  • Pharmaceutical Applications: Due to its unique structure, scientists investigate derivatives of this compound for potential anti-cancer, anti-inflammatory, and anti-viral effects. These applications are essential in drug discovery and development.
  • Structure-Activity Relationship: Studying this compound provides insights into structure-activity relationships (SAR) which is crucial for understanding how modifications in chemical structure can lead to different biological effects.

In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” This compound opens the door to numerous research opportunities, inviting chemists and biologists to unravel its mysteries and potential applications.

In summary, 3-[(4-chlorophenyl)-(2-hydroxy-4-oxo-chromen-3-yl)methyl]-2-hydroxy-chromen-4-one stands as a compelling subject of study in the realms of organic chemistry and pharmacology, reinforcing the interconnectedness of structure and function in the world of chemical compounds.