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Coumestrol

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Identification
Molecular formula
C15H10O5
CAS number
479-13-0
IUPAC name
8-[[bis(2-hydroxyethyl)amino]methyl]-2,6-dihydroxy-4-methyl-chromen-7-one
State
State

Coumestrol is typically found in a solid state at room temperature. It is often used in its crystalline form for various applications.

Melting point (Celsius)
207.00
Melting point (Kelvin)
480.15
Boiling point (Celsius)
612.40
Boiling point (Kelvin)
885.60
General information
Molecular weight
286.25g/mol
Molar mass
286.2810g/mol
Density
1.3920g/cm3
Appearence

Coumestrol is generally present as a yellow crystalline powder. It is often noted for its vibrant color, which can range from pale yellow to deep yellow, depending on its purity and form. The powder is typically fine and can be smoothly distributed in stable solutions when processed correctly.

Comment on solubility

Solubility of 8-[[bis(2-hydroxyethyl)amino]methyl]-2,6-dihydroxy-4-methyl-chromen-7-one

The solubility of 8-[[bis(2-hydroxyethyl)amino]methyl]-2,6-dihydroxy-4-methyl-chromen-7-one can vary significantly depending on several factors. This compound, with its complex structure, contains functional groups that influence its interactions with solvents. Key points regarding its solubility include:

  • Polarity: The presence of hydroxyl (-OH) groups enhances polarity, making the compound more soluble in polar solvents such as water.
  • Hydrogen Bonding: The bis(2-hydroxyethyl)amino group can participate in hydrogen bonding, further facilitating solubility in aqueous solutions.
  • Solvent Compatibility: It is likely to be less soluble in non-polar solvents due to its polar character, favoring polar environments.
  • Temperature Effects: Solubility may increase with temperature, allowing for better dissolution in heated solvents.

In summary, the solubility of this compound is influenced by its functional groups, polarity, and the nature of the solvent. Understanding these factors is crucial for applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about 8-[[bis(2-hydroxyethyl)amino]methyl]-2,6-dihydroxy-4-methyl-chromen-7-one

This fascinating compound, often referred to as a derivative of coumarin, exhibits a wide range of biological activities, making it a subject of avid research among chemists and biochemists alike. Some noteworthy aspects of this compound include:

  • Biological Relevance: Compounds similar to this have demonstrated significant antioxidant properties, which can be crucial in combating oxidative stress in biological systems.
  • Pharmaceutical Potential: The structural features of this compound suggest it may have potential as an anti-inflammatory or anti-cancer agent, drawing interest for further pharmaceutical applications.
  • Multi-functional Structure: The presence of both hydroxyethylaminomethyl and hydroxy groups contributes to the compound's versatility, potentially allowing for numerous interactions in various biological environments.
  • Chemical Stability: Compounds in the coumarin family often exhibit remarkable stability, enhancing their viability for long-term applications in both research and industry.
  • Natural Occurrence: While many derivatives are synthetically produced, some closely related compounds naturally occur in plants, leading to their use in traditional medicine and modern pharmacology.

As emphasized by researchers, "the potentials of hydroxylated coumarin derivatives are vast", opening doors for innovations in drug design and chemical synthesis.

In conclusion, 8-[[bis(2-hydroxyethyl)amino]methyl]-2,6-dihydroxy-4-methyl-chromen-7-one not only showcases an intriguing structure but also encapsulates the intersection of chemistry and biology, making it a prime topic for ongoing studies and exploration.