Fucoxanthin

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Identification

Molecular formula
C42H58O6
CAS Number
3351-86-8
IUPAC Name
2-hydroxy-3-[6-hydroxy-5-[4-methyl-6-(2,6,6-trimethylcyclohexen-1-yl)hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl]-2H-furan-5-one
Molecular Weight
658.93g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1500g/cm3
Synonyms
CBiol_001725
Interesting facts

Interesting Facts about 2-hydroxy-3-[6-hydroxy-5-[4-methyl-6-(2,6,6-trimethylcyclohexen-1-yl)hex-3-enyl]-3,6-dihydro-2H-pyran-2-yl]-2H-furan-5-one

This intriguing compound, commonly referred to as a complex flavonoid derivative, exhibits a rich tapestry of properties and applications that make it a fascinating subject for chemists and researchers alike. Here are some engaging insights about it:

  • Structural Complexity: The compound is distinguished by its intricate structure, boasting multiple chiral centers and functional groups, which contribute to its unique reactivity and biological activities.
  • Natural Occurrence: Derivatives resembling this compound can be found in various plants, notably in those with medicinal qualities. The presence of hydroxyl groups enhances its functionality in biological systems.
  • Potential Health Benefits: Research has indicated that similar compounds may possess antioxidant properties, anti-inflammatory effects, and could play a role in cancer prevention, marking it as a potential candidate for further pharmacological studies.
  • Applications in Natural Products Chemistry: This compound serves as an exemplary model in the synthesis and modification of flavonoid structures, which can lead to the development of new drugs or herbal remedies.
  • Chemical Synthesis: The complex synthesis pathways involved in creating this compound exemplify the challenges faced in organic chemistry, fostering innovative methodologies for organic synthesis among chemists.

As one delves deeper into the study of this compound, the intertwining of its chemical structure, natural occurrence, and potential applications highlights the beauty and complexity of organic chemistry. It encapsulates how a single compound can bridge various domains of science, from biochemistry to medicinal chemistry.

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