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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
State
State

At room temperature, this compound remains in a solid state. Its stability and solid-state form make it easier for handling and storage in laboratory settings.

Melting point (Celsius)
227.00
Melting point (Kelvin)
500.15
Boiling point (Celsius)
541.20
Boiling point (Kelvin)
814.35
General information
Molecular weight
440.36g/mol
Molar mass
440.3600g/mol
Density
1.8000g/cm3
Appearence

This compound appears as a crystalline solid, often off-white in color. The crystalline nature can vary based on the purity and the method of crystallization employed during preparation.

Comment on solubility

Solubility of 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, with the formula C23H14O10, is a complex organic molecule that presents some intriguing characteristics regarding its solubility. Understanding the solubility of such compounds is essential for various applications, particularly in pharmaceuticals and material sciences.

Here are some key factors influencing its solubility:

  • Functional Groups: The presence of carboxylate groups (-COO-) significantly enhances solubility in polar solvents like water, owing to hydrogen bonding and ionic interactions.
  • Molecular Structure: The chromene backbone, which is a larger polycyclic structure, can affect solubility by creating steric hindrances that may limit interaction with solvent molecules.
  • Solvent Polarity: Solubility tends to increase in polar solvents. It may exhibit greater solubility in alcohols or dimethyl sulfoxide (DMSO), compared to non-polar solvents.
  • pH Dependence: As the compound contains acidic functional groups, its solubility may vary with changes in pH, potentially leading to better solubility in basic conditions where the carboxylic groups may deprotonate.

In summary, while the 5-[3-(2-carboxylato-4-oxo-chromen-5-yl)oxy-2-hydroxy-propoxy]-4-oxo-chromene-2-carboxylate is expected to be soluble in polar solvents, the overall solubility can be influenced by multiple factors, including functional groups, molecular structure, and environmental pH levels. Further empirical research would provide definitive data on its solubility profile in various media.

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.

Synonyms
cromoglycate(2-)
Aarane
5-[3-(2-carboxylato-4-oxochromen-5-yl)oxy-2-hydroxypropoxy]-4-oxochromene-2-carboxylate
5,5'-[(2-hydroxypropane-1,3-diyl)bis(oxy)]bis(4-oxo-4H-chromene-2-carboxylate)
UPCMLD-DP013
UPCMLD-DP013:001
CHEBI:59039
BDBM50404862
STL301855
AKOS022139846
NCGC00022858-03
NCGC00022858-04
NCGC00022858-05
NCGC00022858-07
NCGC00178823-01
NCGC00178823-02
AB00513924
AB00053444-09
AB00053444_10
AB00053444_11
Q27126409
5,5'-[(2-hydroxypropane-1,3-diyl)bis(oxy)]bis(4-oxo-4H-1-benzopyran-2-carboxylate)