Scutellarein 7-methyl ether | Solubility of Things

Identification

Molecular formula

C₁₇H₁₄O₈

CAS number

7641-13-0

IUPAC name

4,5-dihydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3,6-dimethoxy-chromen-7-one

State

At room temperature, it is a solid.

Melting point (Celsius)

302.00

Melting point (Kelvin)

575.15

Boiling point (Celsius)

0.00

Boiling point (Kelvin)

0.00

General information

Molecular weight

344.29g/mol

Molar mass

344.3110g/mol

Density

1.4500g/cm³

Appearence

The compound typically appears as a pale yellow crystalline solid.

Comment on solubility

Solubility of 4,5-Dihydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3,6-dimethoxy-chromen-7-one

The solubility of the compound 4,5-dihydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3,6-dimethoxy-chromen-7-one, with the chemical formula C₁₇H₁₄O₈, can be intriguing due to its complex structure featuring multiple hydroxyl and methoxy groups. To understand its solubility, consider the following factors:

Hydroxyl Groups: The presence of hydroxyl (-OH) functional groups significantly increases the hydrophilicity of the compound, making it more soluble in polar solvents, particularly water.
Methoxy Groups: The methoxy (-OCH₃) groups provide a degree of hydrophobic character, which can affect solubility in non-polar solvents.
Overall Structure: The chromen-7-one skeleton influences the electronic distribution within the molecule, impacting its solubility behavior in various solvents.

In summary, the solubility of this compound can vary significantly depending on the solvent used:

Soluble in Water: Due to multiple hydroxyl groups.
Moderately Soluble in Organic Solvents: Perhaps in solvents like ethanol or methanol.
Low Solubility in Non-Polar Solvents: Such as hexane or benzene.

Overall, the balance of hydrophilic and hydrophobic characteristics will dictate the preferred solvent media for this compound, making solubility a fascinating area to explore.

Interesting facts

Interesting Facts About 4,5-dihydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3,6-dimethoxy-chromen-7-one

This intriguing compound belongs to the flavonoid family, which is renowned for its diverse biological activities and health benefits. Here are some fascinating aspects of this specific flavonoid:

Source: This compound can be isolated from various plants, particularly those with traditional medicinal uses, making it an important subject of study in natural product chemistry.
Health Benefits: Flavonoids, including this compound, are often at the forefront of research for their potential antioxidant, anti-inflammatory, and anticancer properties. They play a vital role in maintaining human health and preventing disease.
Bioactivity: Preliminary studies suggest that flavonoids can modulate cellular signaling pathways. This may influence processes such as apoptosis (cell death) and cell proliferation, showcasing their potential in therapeutic applications.
Natural Colorants: Compounds like this one may also contribute to the pigmentation in plants, serving both ecological and aesthetic roles within their natural environments.
Research Interest: Ongoing research continues to explore the structure-activity relationship of flavonoids. The specific substituents of this compound, such as the methoxy and hydroxy groups, may enhance its biological activity and effectiveness.

In summary, 4,5-dihydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3,6-dimethoxy-chromen-7-one is not just a fascinating chemical entity but a beacon of potential in the realm of medicinal chemistry and botanical research. As one scientist aptly stated, "The exploration of nature's compounds often leads to breakthroughs in science and health."