Skip to main content

Daphnetin

ADVERTISEMENT
Identification
Molecular formula
C14H10O6
CAS number
490-38-0
IUPAC name
3,8,10-trihydroxy-3-methyl-7-oxo-1,4-dihydropyrano[4,3-b]chromene-9-carboxylic acid
State
State

Daphnetin is typically found as a solid in powder or crystalline form at room temperature.

Melting point (Celsius)
258.00
Melting point (Kelvin)
531.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
254.23g/mol
Molar mass
254.2060g/mol
Density
1.5520g/cm3
Appearence

The compound typically appears as a crystalline yellow solid.

Comment on solubility

Solubility of 3,8,10-Trihydroxy-3-methyl-7-oxo-1,4-dihydropyrano[4,3-b]chromene-9-carboxylic Acid

The solubility of 3,8,10-trihydroxy-3-methyl-7-oxo-1,4-dihydropyrano[4,3-b]chromene-9-carboxylic acid is a fascinating topic due to its unique structure and functional groups. This compound contains multiple hydroxyl groups, which significantly influence its solubility characteristics.

Key Points about Solubility:

  • Hydroxyl Groups: The presence of three hydroxyl (-OH) groups tends to increase solubility in polar solvents, such as water, due to hydrogen bonding.
  • Carboxylic Acid Group: The -COOH functional group can also enhance the solubility in water through ionization, especially at higher pH levels, converting into an anionic form.
  • Polarity: Overall, the compound is expected to exhibit high solubility in polar solvents and low solubility in non-polar solvents.

In conclusion, due to these various intermolecular interactions, 3,8,10-trihydroxy-3-methyl-7-oxo-1,4-dihydropyrano[4,3-b]chromene-9-carboxylic acid stands out as a compound likely to be soluble in aqueous solutions, making it an interesting subject for further studies in solubility and reactivity.

Interesting facts

Interesting Facts about 3,8,10-trihydroxy-3-methyl-7-oxo-1,4-dihydropyrano[4,3-b]chromene-9-carboxylic acid

This compound, known for its complex structure and biological significance, is a fascinating subject of study in the realm of organic chemistry and pharmacology. Here are some interesting facts:

  • Structural Diversity: The compound exhibits a unique fused ring structure, which includes both chromene and pyran moieties. This heterocyclic nature contributes to its diverse chemical reactivity and potential applications.
  • Natural Occurrence: Variants of this compound are often found in natural sources, particularly in plants with medicinal properties, indicating its potential as a bioactive compound.
  • Therapeutic Potential: Research suggests that compounds with similar structures possess a range of pharmacological activities, including antioxidant, anti-inflammatory, and anticancer properties.
  • Enzymatic Interactions: The presence of multiple hydroxyl (-OH) groups enhances the compound's ability to interact with enzymes, potentially influencing metabolic pathways.
  • Research Application: Its complex chemical structure makes it an interesting target for synthetic chemistry, allowing scientists to explore new synthetic routes and modifications to enhance its efficacy.

As a result, 3,8,10-trihydroxy-3-methyl-7-oxo-1,4-dihydropyrano[4,3-b]chromene-9-carboxylic acid stands out not only for its intricate design but also for how it embodies the intersection of natural products and synthetic chemistry. In the words of a renowned chemist, “The beauty of chemistry lies not just in the substances we create but in the stories they tell about nature’s ingenuity.”