Coumarin Dimer

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Identification

Molecular formula
C18H12O5
CAS Number
118-60-5
IUPAC Name
2-hydroxy-3-[(2-hydroxy-4-oxo-chromen-3-yl)methyl]chromen-4-one
Molecular Weight
290.25g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3960g/cm3
Interesting facts

Exploring 2-Hydroxy-3-[(2-hydroxy-4-oxo-chromen-3-yl)methyl]chromen-4-one

2-Hydroxy-3-[(2-hydroxy-4-oxo-chromen-3-yl)methyl]chromen-4-one, often referred to as a type of coumarin derivative, presents fascinating attributes that make it an interesting subject of study within organic chemistry and medicinal applications. Below are some compelling facts about this compound:

  • Flavonoid Family: This compound belongs to the flavonoid class of secondary metabolites, which are widely recognized for their antioxidant properties and potential health benefits.
  • Natural Sources: It can be found in various plants, contributing to their pigmentation and occasionally acting as a defense mechanism against pathogens and herbivores.
  • Antioxidant Activity: Research has suggested that this compound may exhibit significant antioxidant activity, making it a candidate for further studies on its protective effects against oxidative stress.
  • Pharmacological Potential: The presence of the chromen-4-one structure provides this compound with a basis for exploring pharmacological applications, possibly including anti-inflammatory and anticancer properties.
  • Functional Groups: The hydroxyl (-OH) groups in its structure enhance its ability to participate in various chemical reactions, potentially allowing for modifications that could improve its bioactivity.

In summary, 2-hydroxy-3-[(2-hydroxy-4-oxo-chromen-3-yl)methyl]chromen-4-one is a representative of a class of compounds that blend intricate chemistry with considerable potential for various applications. As research continues to unfold, this molecule may reveal more secrets and become a significant player in the fields of pharmaceuticals and natural products.

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