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Daidzein

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Identification
Molecular formula
C15H10O4
CAS number
486-66-8
IUPAC name
2,4-dihydroxy-3-phenyl-chromen-7-one
State
State

At room temperature, daidzein is in a solid state, specifically as a powder.

Melting point (Celsius)
315.00
Melting point (Kelvin)
588.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
254.24g/mol
Molar mass
254.2410g/mol
Density
1.4360g/cm3
Appearence

Daidzein is a white to off-white crystalline powder.

Comment on solubility

Solubility of 2,4-Dihydroxy-3-phenyl-chromen-7-one

The solubility of 2,4-dihydroxy-3-phenyl-chromen-7-one exhibits a noteworthy characteristic that can be greatly influenced by various factors:

  • Polarity: The presence of hydroxyl groups (-OH) lends a degree of polarity to the molecule, potentially enhancing solubility in polar solvents such as water.
  • Solvent Selection: This compound is generally more soluble in organic solvents like ethanol or methanol rather than in non-polar solvents. Thus, the choice of solvent plays a crucial role.
  • pH Dependence: The solubility can also be affected by the pH of the solution, as the ionization of the hydroxyl groups may vary under different pH conditions.

In summary, the solubility of 2,4-dihydroxy-3-phenyl-chromen-7-one is largely dictated by its structural features, the solvent being used, and the environmental conditions such as pH. As with many organic compounds, it's important to consider these factors to fully understand its solubility properties.

Interesting facts

Interesting Facts about 2,4-Dihydroxy-3-phenyl-chromen-7-one

2,4-Dihydroxy-3-phenyl-chromen-7-one, commonly referred to as a flavonoid compound, presents a fascinating area of study in both organic chemistry and pharmacology. Here are some intriguing insights about this compound:

  • Flavonoid Family: This compound belongs to the flavonoid class, known for their vibrant colors in many plants. They play essential roles in plant pigmentation and UV filtration.
  • Biological Activities: Flavonoids, including this one, showcase a variety of biological activities. Research has indicated that they can have antioxidant, anti-inflammatory, and potential anticancer properties.
  • Chemical Versatility: This compound features several hydroxyl (-OH) groups, enhancing its solubility and making it versatile in terms of reactivity and functionality.
  • Natural Sources: It can be found in various plants, contributing to their medicinal properties. Traditional medicine often utilizes flavonoids for their health benefits.
  • Structure-Lactivity Relationship: The specific arrangement of its phenyl and chromenone structure is crucial for its biological effects. This relationship is a key focus for scientists developing new pharmaceuticals.

As researchers delve deeper into the properties of 2,4-dihydroxy-3-phenyl-chromen-7-one, they continue to uncover its potential applications in the fields of medicine, nutrition, and beyond.

In summary, the study of this compound not only enriches our understanding of flavonoids but also opens new avenues for therapeutic interventions. Its distinct chemical structure and promising biological activities make it a valuable subject for ongoing scientific investigation.