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Coumarin 6

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Identification
Molecular formula
C24H16O3
CAS number
38215-36-0
IUPAC name
(2-oxo-3,4-diphenyl-chromen-7-yl) acetate
State
State

At room temperature, (2-oxo-3,4-diphenyl-chromen-7-yl) acetate is in a solid state.

Melting point (Celsius)
216.00
Melting point (Kelvin)
489.15
Boiling point (Celsius)
362.00
Boiling point (Kelvin)
635.15
General information
Molecular weight
350.38g/mol
Molar mass
350.3580g/mol
Density
1.1950g/cm3
Appearence

(2-Oxo-3,4-diphenyl-chromen-7-yl) acetate appears as an orange powder. It is commonly used as a dye due to its strong fluorescence.

Comment on solubility

Solubility of (2-oxo-3,4-diphenyl-chromen-7-yl) acetate

The solubility of (2-oxo-3,4-diphenyl-chromen-7-yl) acetate can be a complex topic due to its unique structural characteristics. Here are some key points to consider:

  • Polarity: The presence of the acetate functional group contributes to the polarity of this compound, potentially enhancing its solubility in polar solvents.
  • Solvent Compatibility: Generally, this compound is expected to dissolve well in organic solvents such as ethanol, acetone, and dichloromethane.
  • Water Solubility: Given its hydrophobic phenyl groups, (2-oxo-3,4-diphenyl-chromen-7-yl) acetate is likely to have limited solubility in water, as aromatic compounds typically exhibit low affinity for polar solvents.
  • Temperature Effects: Solubility may increase with temperature; thus, higher temperatures can be beneficial for dissolving the compound in a given solvent.

In summary, while (2-oxo-3,4-diphenyl-chromen-7-yl) acetate demonstrates good solubility in non-polar and some polar organic solvents, its interaction with water is constricted due to its hydrophobic characteristics. Always consult specific solubility data for practical applications.

Interesting facts

Interesting Facts about (2-oxo-3,4-diphenyl-chromen-7-yl) acetate

(2-oxo-3,4-diphenyl-chromen-7-yl) acetate is a fascinating compound belonging to the class of flavonoids. These compounds are well-known for their diverse biological activities and are frequently studied in medicinal chemistry. Here are some interesting highlights regarding this specific compound:

  • Flavonoid Family: As a member of the flavonoid family, this compound exhibits a variety of biological properties, including antioxidant, anti-inflammatory, and anticancer effects. Such attributes make it a subject of extensive research for drug discovery.
  • Structure-Activity Relationship: The unique structure of (2-oxo-3,4-diphenyl-chromen-7-yl) acetate allows scientists to investigate how modifications to the flavonoid nucleus could enhance activity, opening doors in pharmacological research.
  • Natural Sources: Compounds similar to (2-oxo-3,4-diphenyl-chromen-7-yl) acetate are often found in a variety of plants, particularly in fruits, vegetables, and herbs. The presence of flavonoids in our diet is believed to contribute to health benefits.
  • Potential Applications: Research is ongoing to harness this compound’s properties for applications in various fields, from cosmetics that target skin aging to therapies in disease management and prevention.
  • Chemical Synthesis: The synthesis of this compound can be achieved via various methods, providing an excellent opportunity for organic chemists to explore creative synthetic pathways that can lead to the development of novel compounds.

In summary, (2-oxo-3,4-diphenyl-chromen-7-yl) acetate isn't just a chemical entity; it represents the intersection of nature and science, promising potential benefits through its various applications in health and industry. As research progresses, who knows what remarkable discoveries await this compound!

Synonyms
1508-89-0
BRN 0041836
Acetic acid 3,4-diphenyl-2-oxo-2H-benzopyran-7-yl ester
3,4-Diphenyl-7-hydroxycoumarin acetate (ester)
COUMARIN, 3,4-DIPHENYL-7-HYDROXY-, ACETATE (ester)
DTXSID10934064
2-Oxo-3,4-diphenyl-2H-1-benzopyran-7-yl acetate