Coumarin Dimer
- 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
Identification
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.