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Orobol

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Identification
Molecular formula
C16H12O7
CAS number
480-23-9
IUPAC name
2,6,8-trihydroxy-3-(4-methoxyphenyl)chromen-4-one
State
State

At room temperature, orobol is typically found in a solid state.

Melting point (Celsius)
314.00
Melting point (Kelvin)
587.15
Boiling point (Celsius)
534.00
Boiling point (Kelvin)
807.15
General information
Molecular weight
302.26g/mol
Molar mass
302.2630g/mol
Density
1.4206g/cm3
Appearence

Orobol is a yellow crystalline solid. It exhibits a bright yellow hue due to its chromen structure and conjugation, which absorbs specific wavelengths of light. The crystals can be described as elongated and exhibit good clarity.

Comment on solubility

Solubility of 2,6,8-trihydroxy-3-(4-methoxyphenyl)chromen-4-one

The solubility of 2,6,8-trihydroxy-3-(4-methoxyphenyl)chromen-4-one can be intriguing due to its complex structure and functional groups. Here are some key points concerning its solubility:

  • Polarity: The presence of multiple hydroxyl (-OH) groups suggests that this compound may exhibit improved solubility in polar solvents such as water.
  • Solvent Interactions: This compound may also dissolve well in organic solvents like ethanol and acetonitrile, particularly due to the methoxy phenyl group which provides hydrophobic characteristics.
  • pH Dependency: The solubility can vary significantly with pH. Under acidic or basic conditions, the ionization of hydroxyl groups can enhance solubility.
  • Temperature Effects: Generally, increasing temperature can lead to greater solubility in both polar and non-polar solvents.

As one statement summarizes: "The solubility is a dance of polarity and functional interactions." Thus, understanding the solubility properties of this compound can lead to valuable insights in various applications, from pharmaceuticals to materials science.

Interesting facts

Interesting Facts about 2,6,8-Trihydroxy-3-(4-methoxyphenyl)chromen-4-one

2,6,8-Trihydroxy-3-(4-methoxyphenyl)chromen-4-one is a fascinating compound with a variety of intriguing properties and applications. Often linked to the family of flavonoids, it showcases several noteworthy aspects:

  • Plant-Derived Origin: As a flavonoid, this compound is typically found in various plants, playing a crucial role in their color and providing UV protection.
  • Antioxidant Properties: It is known for its potent antioxidant capabilities, which can help combat oxidative stress in biological systems.
  • Pharmacological Potential: Research suggests that it has potential therapeutic effects, including anti-inflammatory and anti-cancer properties.
  • Mechanism of Action: This compound’s efficacy may be attributed to its ability to scavenge free radicals and modulate various signaling pathways in the body.
  • Bioavailability: Its unique chemical structure may influence how the body absorbs and utilizes this compound, making it a topic of interest for further study.

In the words of noted chemists, “The beauty of nature’s compounds lies in their intricate structures and the promises they hold for human health.” As research continues to unveil the secrets of 2,6,8-trihydroxy-3-(4-methoxyphenyl)chromen-4-one, its applications in health and medicine could expand significantly, making it a compound worthy of attention.

In conclusion, the exploration of 2,6,8-trihydroxy-3-(4-methoxyphenyl)chromen-4-one not only highlights the remarkable connections between chemistry and nature but also encourages scientists to delve deeper into the potential benefits of plant-derived compounds.