Norepinephrine | Solubility of Things

Identification

Molecular formula

C₁₅H₁₀O₅

CAS number

17833-53-3

IUPAC name

4,5-dihydroxy-2-(4-hydroxyphenyl)chromen-7-one

State

At room temperature, 4,5-dihydroxy-2-(4-hydroxyphenyl)chromen-7-one exists as a solid in the form of crystalline material. It is generally stable and can be manipulated in most laboratory environments without additional constraints to temperature and pressure.

Melting point (Celsius)

216.00

Melting point (Kelvin)

489.15

Boiling point (Celsius)

684.15

Boiling point (Kelvin)

957.30

General information

Molecular weight

272.24g/mol

Molar mass

272.2570g/mol

Density

1.4800g/cm³

Appearence

4,5-dihydroxy-2-(4-hydroxyphenyl)chromen-7-one is a flavonoid compound. It typically appears as a pale yellow to orange crystalline solid when isolated. The crystalline form may exhibit varying shades depending on purity and specific hydration states.

Comment on solubility

Solubility of 4,5-Dihydroxy-2-(4-hydroxyphenyl)chromen-7-one

The solubility of 4,5-dihydroxy-2-(4-hydroxyphenyl)chromen-7-one, represented by the chemical formula C₁₅H₁₀O₅, can be characterized as follows:

Polar and Non-Polar Solvents: This compound is expected to show varying solubility in different solvents due to the presence of multiple hydroxyl (-OH) groups which increase hydrophilicity.
Water Solubility: It is likely to exhibit some degree of solubility in water due to the hydroxyl functionalities that can form hydrogen bonds.
Organic Solvents: Given its organic structure, 4,5-dihydroxy-2-(4-hydroxyphenyl)chromen-7-one may also dissolve well in organic solvents such as ethanol or methanol.

In practice, solubility testing should be conducted to determine the exact solubility profile in a range of solvents, as factors such as temperature and pH can significantly affect its solubility characteristics. As a general observation in organic compounds, compounds containing multiple hydroxyl groups tend to solubilize better in polar solvents. Thus, it can be concluded that while this chromenone derivative has useful properties, its solubility will vary in different environments.

Interesting facts

Interesting Facts about 4,5-Dihydroxy-2-(4-hydroxyphenyl)chromen-7-one

4,5-Dihydroxy-2-(4-hydroxyphenyl)chromen-7-one is a compelling compound that draws interest in the fields of both organic chemistry and biochemistry. Here are some intriguing insights:

Natural Sources: This compound is typically derived from natural sources, often found in various plants. Its presence highlights the diverse roles of flavonoids, a class to which it belongs, in the plant kingdom.
Biological Activity: Known for its antioxidant properties, this compound plays a significant role in the protection of cells against oxidative stress, which is linked to various health issues, including aging and chronic diseases.
Pharmacological Potential: Research suggests that compounds like 4,5-dihydroxy-2-(4-hydroxyphenyl)chromen-7-one may have anti-inflammatory and anti-cancer effects. These findings open avenues for potential therapeutic applications in modern medicine.
Structure-Activity Relationship: The unique chromenone structure, characterized by a fused benzopyran system with hydroxyl groups, is essential for its biological activity. This highlights the importance of chemical structure in influencing the properties and reactivities of organic compounds.
Chemical Reactions: This compound exhibits interesting reactivity patterns, allowing it to participate in various chemical reactions, making it a valuable subject of study for synthetic organic chemists.

As stated by renowned chemists, "The true beauty of organic chemistry lies in its complexity and diversity," and 4,5-dihydroxy-2-(4-hydroxyphenyl)chromen-7-one is a perfect illustration of this principle.

In summary, this compound not only signifies the intricate designs of nature but also offers exciting prospects in scientific research and potential applications in medicine and health.