Skip to main content

3-Ethylchromone

ADVERTISEMENT
Identification
Molecular formula
C11H10O2
CAS number
38512-54-0
IUPAC name
3-ethylchromen-4-one
State
State

3-Ethylchromone is typically a solid at room temperature. It is stable under normal conditions but should be stored in a cool, dry place to prevent degradation.

Melting point (Celsius)
51.00
Melting point (Kelvin)
324.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
172.20g/mol
Molar mass
172.1990g/mol
Density
1.1700g/cm3
Appearence

3-Ethylchromone is a pale yellow to off-white crystalline solid. It has a characteristic odor that is often associated with chromones and can form distinct crystals under suitable conditions.

Comment on solubility

Solubility of 3-ethylchromen-4-one

3-ethylchromen-4-one, a compound known for its unique structure, displays interesting solubility properties influenced by its chemical nature. Its solubility can be understood as follows:

  • Polar vs Nonpolar: 3-ethylchromen-4-one exhibits a relatively nonpolar character due to its aromatic ring structure, which limits its solubility in polar solvents.
  • Solvents: The compound is better soluble in nonpolar organic solvents such as:
    • Hexane
    • Toluene
    • Chloroform
  • Water Solubility: It has low solubility in water, which is characteristic of many aromatic compounds due to their inability to effectively interact with water molecules.
  • Temperature Dependency: Like many organic compounds, solubility can increase with temperature, making it more soluble in hot organic solvents.

In summary, the solubility of 3-ethylchromen-4-one highlights the balance between its structural properties and interactions with solvents, reinforcing the principle that “like dissolves like.” The molecule's nonpolar characteristics predominantly guide its solubility preferences towards nonpolar environments.

Interesting facts

Interesting Facts about 3-ethylchromen-4-one

The compound 3-ethylchromen-4-one belongs to the flavonoids group, which are known for their diverse biological activities and widespread occurrence in plants. This particular compound has piqued the interest of scientists due to its unique structure and potential applications in various fields.

Biological Significance

3-ethylchromen-4-one exhibits a range of biological properties, including:

  • Antioxidant Activity: This compound has been shown to scavenge free radicals, thereby protecting cells from oxidative stress.
  • Anti-inflammatory Effects: Studies suggest that 3-ethylchromen-4-one may help reduce inflammation, which is a critical factor in many chronic diseases.
  • Antimicrobial Properties: It may possess certain capabilities to inhibit the growth of various microbes, making it a potential candidate for pharmaceutical applications.

Chemical Structure and Properties

The structure of 3-ethylchromen-4-one includes a chromenone backbone, which contributes to its reactivity and interaction with biological systems. Here are some aspects of its structure to note:

  • Chromene Ring System: This bicyclic structure is pivotal in determining the compound's chemical behavior.
  • Functional Groups: The ethyl group enhances the lipophilicity of the compound, potentially influencing its bioavailability.

Applications Beyond Biology

Beyond its biological significance, 3-ethylchromen-4-one shows promise in:

  • Pharmaceutical Development: It is being researched for its capabilities in developing new drugs, particularly in the areas of anti-cancer and anti-diabetic therapies.
  • Natural dyes: The chromenone structure is also utilized in creating natural dyes, lending it importance in the textile and cosmetic industries.

Final Thoughts

Overall, 3-ethylchromen-4-one represents a fascinating intersection of chemistry and biology, with potential implications for health and industry. As research continues, it may unlock new avenues for therapeutic interventions and innovative applications.

Synonyms
3-Ethylchromone
2-Ethylchromone
NSC 71387
Ethyl-3 chromone [French]
CHROMONE, 3-ETHYL-
Ethyl-3 chromone
4H-1-Benzopyran-4-one, 2-ethyl-
L.B.C 181
Chromone, 2-ethyl-
BRN 0124317
AI3-03078
SCHEMBL292868
SCHEMBL12655257
4-17-00-05093 (Beilstein Handbook Reference)