Coumarin derivative | Solubility of Things

Identification

Molecular formula

C₂₂H₁₄O₈

CAS number

7748-75-2

IUPAC name

ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate

State

At room temperature, ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate exists as a solid. It is typically in a crystalline form and is stable under standard conditions.

Melting point (Celsius)

204.00

Melting point (Kelvin)

477.00

Boiling point (Celsius)

581.00

Boiling point (Kelvin)

854.00

General information

Molecular weight

394.36g/mol

Molar mass

394.3610g/mol

Density

1.3260g/cm³

Appearence

The compound is generally a pale yellow solid that can vary slightly in hue depending on the exact molecular structure and purity. It may appear crystalline and is often as a powder or small granules.

Comment on solubility

Solubility of Ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate

Understanding the solubility of ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate can offer insights into its potential applications and behavior in various environments. Here are some key points regarding its solubility:

Organic Solvents: This compound is expected to exhibit good solubility in organic solvents due to its hydrophobic chromenone moieties. Solvents like ethanol, methanol, and DMSO may dissolve this compound effectively.
Aqueous Solubility: The presence of the hydroxyl group could impart some level of solubility in water, however, the overall hydrophobic nature may limit this. It is important to test specific conditions.
pH Dependence: The solubility might be influenced by the pH of the solution. Under certain pH conditions, the ionization of the hydroxyl group may enhance solubility.
Temperature Effects: Generally, increased temperature can enhance solubility. Therefore, conducting solubility tests at various temperatures may provide critical insights.

In conclusion, while the solubility of ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate in water might be limited, its solubility in organic solvents should be much better, making it suitable for a variety of chemical and pharmaceutical applications. Always remember to evaluate specific conditions for accurate solubility data!

Interesting facts

Exploring Ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate

Ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate is a fascinating compound belonging to the family of flavonoids, which are known for their diverse biological activities. Here are some intriguing aspects of this compound:

Flavonoid Structure: The compound features a complex flavonoid structure, characterized by the presence of chromen-3-yl units. Flavonoids are renowned for their antioxidant properties, which can help protect cells from oxidative stress.
Biological Activity: Research indicates that compounds like this one demonstrate potential therapeutic effects, including anti-inflammatory and antimicrobial properties. Such activities make it a subject of interest in pharmaceutical studies.
Natural Sources: Flavonoids, including this compound, can often be found in various plants and are integral to many plant-based diets. They contribute to the vibrant colors of fruits and flowers.
Chemical Reactivity: The functionalities present in ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate may allow for interesting chemical reactions, opening avenues for new synthetic derivatives.
Applications in Research: Studies of this compound can contribute to the understanding of natural product chemistry and its applications in drug design, especially in the context of developing new antioxidants.

In summary, ethyl 2-(2-hydroxy-4-oxo-chromen-3-yl)-2-(4-oxochromen-3-yl)acetate represents a blend of beauty and utility in the realm of chemistry, sparking interest in its potential applications and effects in various biological systems. As we explore such compounds, we deepen our understanding of their roles in both nature and medicine.