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Kuwanol E

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Identification
Molecular formula
C25H26O6
CAS number
66056-22-8
IUPAC name
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one
State
State

At room temperature, Kuwanol E is a solid compound.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.13
Boiling point (Celsius)
583.13
Boiling point (Kelvin)
856.28
General information
Molecular weight
426.47g/mol
Molar mass
426.4720g/mol
Density
1.4260g/cm3
Appearence

Kuwanol E typically appears as a solid, pale yellow crystalline powder. Its crystalline appearance is due to its well-defined chemical structure.

Comment on solubility

Solubility of 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one

The compound 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one, with the chemical formula C25H26O6, exhibits interesting solubility characteristics that can influence its applications in various fields.

Solubility Insights:

  • General Solubility: This compound is typically soluble in organic solvents such as ethanol and methanol, but demonstrates limited solubility in water.
  • Polarity Consideration: The presence of multiple hydroxyl groups (-OH) suggests that there are polar characteristics which can enhance solubility in polar organic solvents.
  • Intermolecular Interactions: Hydrogen bonding capabilities due to -OH groups can create stronger interactions in solvents with similar properties.
  • Practical Applications: The solubility in organic solvents makes it particularly suitable for formulations in pharmaceuticals and cosmetics.

In summary, while 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one is not highly soluble in water, its solubility in various organic solvents can be leveraged in specific applications. As such, understanding solubility is crucial for optimizing its use in chemical formulations.

Interesting facts

Interesting Facts about 3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one

The compound known as 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one is a fascinating member of the flavonoid family, which may play significant roles in various biological processes. Here are some intriguing aspects of this compound:

  • Natural Origins: Many flavonoids, including this compound, are derived from plant sources. They often exhibit antioxidant properties, which help protect plants from environmental stresses.
  • Biological Activity: Research indicates that flavonoids can have multiple health benefits, including anti-inflammatory and anti-cancer effects, making such compounds of interest in medicinal chemistry.
  • Structural Diversity: The specific arrangement of hydroxyl groups and various substituents on the chromenone scaffold contributes to the compound's unique chemical behavior and biological activity.
  • Functional Applications: Compounds like this one are being studied in food science and nutrition due to their potential roles in improving health and preventing chronic diseases.

Incorporating such compounds into dietary choices may lead to enhanced health benefits. As the famous chemist Linus Pauling said, "You can trace every sickness, every disease, and every ailment to a mineral deficiency." Thus, understanding compounds like 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)chromen-4-one could be the key to uncovering how nature provides tools for our wellbeing.


The study of such complex organic compounds highlights the interplay between chemistry and health and encourages further exploration into the myriad of natural products at our disposal.

Synonyms
6,8-Diprenylkaempferol
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
CHEMBL516427
LMPK12111988
NSC721159
NSC-721159