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Flavokawain A

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Identification
Molecular formula
C17H16O3
CAS number
3420-72-4
IUPAC name
3-(3,5-dimethylphenyl)-2-hydroxy-chromen-4-one
State
State

At room temperature, Flavokawain A is typically found in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
147.00
Melting point (Kelvin)
420.15
Boiling point (Celsius)
388.00
Boiling point (Kelvin)
661.15
General information
Molecular weight
268.32g/mol
Molar mass
268.2950g/mol
Density
1.2560g/cm3
Appearence

Flavokawain A is typically a pale yellow crystalline solid with a characteristic appearance due to its chromenone structure. It may appear as a powder or crystal and is often used in scientific research.

Comment on solubility

Solubility of 3-(3,5-dimethylphenyl)-2-hydroxy-chromen-4-one

The solubility of 3-(3,5-dimethylphenyl)-2-hydroxy-chromen-4-one, a compound belonging to the flavonoid family, exhibits interesting characteristics influenced by its chemical structure. Generally, flavonoids can display variable solubility in different solvents, and this compound is no exception.

Key Solubility Characteristics:

  • Polar Solvents: The presence of a hydroxy group (-OH) enhances the ability of this compound to dissolve in polar solvents, such as methanol and ethanol, due to hydrogen bonding.
  • Non-Polar Solvents: Conversely, non-polar solvents like hexane may result in lower solubility. This is primarily due to the hydrophobic effects of the aromatic rings present in the structure.
  • Overall Solubility: The solubility can vary based on factors such as temperature and the molecular interactions within the solvent.

In practical applications, the solubility behavior is crucial, as it affects the compound's bioavailability and efficacy in various formulations. Overall, while it shows favorable solubility in polar solvents, researchers must account for its limited solubility in non-polar environments when developing formulations.

Interesting facts

Interesting Facts About 3-(3,5-Dimethylphenyl)-2-Hydroxy-Chromen-4-One

3-(3,5-Dimethylphenyl)-2-hydroxy-chromen-4-one, often referred to as a flavonoid compound, is a captivating molecule with a variety of noteworthy characteristics. This compound belongs to the class of natural products known as flavones, which are distinguished by their benzopyrone structure and exhibit a range of biological activities.

Biological Significance

  • Antioxidant Properties: Flavones, including this compound, are known for their ability to scavenge free radicals, helping to protect cells from oxidative stress.
  • Anti-inflammatory Effects: Studies suggest that flavonoids can modulate inflammatory pathways, making them a focus of research in treating inflammatory diseases.
  • Potential Anticancer Activity: Some research indicates that compounds like 3-(3,5-dimethylphenyl)-2-hydroxy-chromen-4-one may exhibit anticancer properties through mechanisms such as apoptosis induction.

Applications in Research and Industry

This complex molecule is not only interesting from a biological perspective but also has practical applications:

  • Pharmaceutical Development: Due to its biological activities, it is being explored as a lead compound for developing new drugs.
  • Natural Dye: The chromen-4-one backbone provides vibrant colors, making it suitable for use in natural dye formulations.
  • Food Additive: As an antioxidant, it may be incorporated into food products to extend shelf life and enhance nutritional value.

Chemical Properties and Synthesis

From a synthetic chemistry perspective, researchers are fascinated by the various methods to synthesize this flavonoid. These can include:

  • Condensation Reactions: Utilized for forming the chromen backbone.
  • Hydroxylation Processes: Essential for introducing the hydroxy group at the 2-position, crucial for its biological activity.

As a student or scientist studying this compound, one may be particularly intrigued by the interplay between its structure and function, as it showcases how small changes in molecular architecture can lead to significant differences in biological activity. The exploration of 3-(3,5-dimethylphenyl)-2-hydroxy-chromen-4-one continues to yield promising results in various fields of science, underscoring the importance of flavonoids in both health and industry.