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Identification
Molecular formula
C25H18O5
CAS number
Not available
IUPAC name
[4-[3-(4-methoxyphenyl)-2-oxo-chromen-4-yl]phenyl] acetate
State
State

This compound is likely a solid at room temperature given its molecular structure and the common properties of similar compounds.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
398.41g/mol
Molar mass
0.0000g/mol
Density
0.0000g/cm3
Appearence

This compound is expected to be a crystalline solid given its structure and molecular composition. However, specific appearance details are not readily available and may require empirical observation.

Comment on solubility

Solubility Characteristics of [4-[3-(4-methoxyphenyl)-2-oxo-chromen-4-yl]phenyl] acetate

The solubility of [4-[3-(4-methoxyphenyl)-2-oxo-chromen-4-yl]phenyl] acetate can be understood through a combination of several key factors:

  • Polarity: The compound contains both polar and non-polar regions, contributed by the methoxy and acetate groups, which influences its solubility in polar and non-polar solvents.
  • Solvent Interactions: It is likely to exhibit better solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO) due to its aromatic structure.
  • Temperature Effects: Solubility may increase with temperature, as is common with organic compounds, which can enhance molecular interactions.
  • Functional Groups: The presence of methoxy and acetate groups suggests that it could form hydrogen bonds with polar solvents, aiding in solubility.

In summary, while the specific solubility data for [4-[3-(4-methoxyphenyl)-2-oxo-chromen-4-yl]phenyl] acetate might not be extensively documented, understanding its structure allows for the hypothesis that it will be soluble in a range of organic solvents, particularly in warmer conditions. Observing the compound's interaction in different solvents can provide further insights into its solubility behavior.

Interesting facts

Interesting Facts about 4-[3-(4-methoxyphenyl)-2-oxo-chromen-4-yl]phenyl acetate

This intriguing compound belongs to the class of organic molecules recognized for their rich pharmacological properties. Chemists and biologists alike are drawn to compounds like this for their versatility and potential applications in medicine.

Key Characteristics

  • Functional Groups: The compound features various functional groups, such as the ester group, which often enhances the biological activity and solubility of compounds.
  • Chromen-4-yl Framework: The presence of the chromen-4-yl moiety indicates a possible involvement in various biological activities, including antihypertensive, anti-inflammatory, and antioxidant effects.
  • Methoxy Substituent: The methoxy group present in the phenyl structure may contribute to increased lipophilicity, enhancing the compound's ability to cross biological membranes.

Potential Applications

Given its structure, 4-[3-(4-methoxyphenyl)-2-oxo-chromen-4-yl]phenyl acetate could be explored for:

  • Therapeutic Uses: Compounds of this nature have been studied for their potential in treating various ailments, including cancer and cardiovascular diseases.
  • Biological Research: This compound can serve as a lead compound in drug development, especially when exploring new anti-cancer drugs.
  • Agricultural Applications: Many phenolic compounds are investigated for their antifungal and antibacterial properties, which could benefit agricultural practices.

In summary, the compound 4-[3-(4-methoxyphenyl)-2-oxo-chromen-4-yl]phenyl acetate holds exciting potential for future studies. Its unique structure combined with diverse applications makes it a valuable subject of research in the fields of medicinal and organic chemistry. As noted by scientists: "Understanding these complex compounds opens the door to innovative solutions in medicine and agriculture."

Synonyms
1508-91-4
COUMARIN, 4-(p-HYDROXYPHENYL)-3-(p-METHOXYPHENYL)-, ACETATE (ester)
BRN 1298476
4-(p-Hydroxyphenyl)-3-(p-methoxyphenyl)coumarin acetate (ester)
5RYP8CW65A
DTXSID80164614
Coumarin, 4-(p-hydroxyphenyl)-3-(p-methoxyphenyl)-, acetate
2H-1-Benzopyran-2-one, 4-[4-(acetyloxy)phenyl]-3-(4-methoxyphenyl)-
4-[4-(Acetyloxy)phenyl]-3-(4-methoxyphenyl)-2H-1-benzopyran-2-one