Hymecromone (7-Hydroxy-4-methylcoumarin) Derivative

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Identification

Molecular formula
C23H14O10
CAS Number
14957-74-7
IUPAC Name
5-[3-(2-carboxylato-4-oxo-chromen-5-yl)oxy-2-hydroxy-propoxy]-4-oxo-chromene-2-carboxylate
Molecular Weight
440.36g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.8000g/cm3
Synonyms
cromoglycate(2-)
Interesting facts

Exploring 5-[3-(2-carboxylato-4-oxo-chromen-5-yl)oxy-2-hydroxy-propoxy]-4-oxo-chromene-2-carboxylate

The compound 5-[3-(2-carboxylato-4-oxo-chromen-5-yl)oxy-2-hydroxy-propoxy]-4-oxo-chromene-2-carboxylate belongs to the class of chromenes, which are fascinating due to their extensive array of biological activities and structural versatility. Here are some interesting facts about this compound:

  • Versatile Structure: The chromene framework is notable for its ability to undergo various chemical modifications, which enhances its functional potential in different applications.
  • Biological Activity: Compounds within the chromene family have shown promising results as antioxidants, anti-inflammatory agents, and even in exhibiting anticancer properties.
  • Pharmacological Interest: The presence of carboxylate groups in the structure indicates potential for chelation and can play a role in enhancing the solubility and bioavailability of therapeutic drugs.
  • Natural Occurrence: Many chromenes are found in natural products, particularly in plants where they often contribute to pigmentation and protection against UV radiation.
  • Research Applications: Scientists are increasingly interested in synthesizing and modifying chromene derivatives for drug development, particularly in the fields of medicinal chemistry and pharmacognosy.

Overall, the combination of a complex chromene structure and the functional groups attached to it suggests a wealth of potential for further study and application, making this compound a captivating subject in chemical research.

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