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Hirsutic Acid C

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Identification
Molecular formula
C12H14O2
CAS number
51779-45-0
IUPAC name
3-ethyl-3-phenyl-tetrahydrofuran-2-one
State
State

At room temperature, 3-ethyl-3-phenyl-tetrahydrofuran-2-one is in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
190.25g/mol
Molar mass
190.2530g/mol
Density
1.1000g/cm3
Appearence

The compound 3-ethyl-3-phenyl-tetrahydrofuran-2-one is typically found as a colorless to pale yellow liquid. It has a pleasant aromatic odor associated with many organic esters and lactones.

Comment on solubility

Solubility of 3-ethyl-3-phenyl-tetrahydrofuran-2-one

The solubility of 3-ethyl-3-phenyl-tetrahydrofuran-2-one can be influenced by various factors, including its molecular structure and the nature of the solvent. Being a tetrahydrofuran derivative, it has a unique cyclic structure that contributes to its solubility characteristics.

Key points regarding its solubility include:

  • Polar and Nonpolar Solvents: This compound may exhibit varying solubility in polar and nonpolar solvents due to the presence of both ethyl and phenyl groups, which can hinder complete solvation in polar environments.
  • Saturation: The solubility may reach saturation at certain concentrations, making it essential to identify the maximum amount that can dissolve in a specific solvent.
  • Temperature Dependence: Like many organic compounds, the solubility of 3-ethyl-3-phenyl-tetrahydrofuran-2-one can vary with temperature. Increased temperatures generally lead to improved solubility.

In summary, the solubility of 3-ethyl-3-phenyl-tetrahydrofuran-2-one is determined by its structural properties and interactions with various solvents. Understanding these aspects is crucial for applications in chemical synthesis and industrial processes.

Interesting facts

Interesting Facts about 3-Ethyl-3-phenyl-tetrahydrofuran-2-one

3-Ethyl-3-phenyl-tetrahydrofuran-2-one, often referred to in the scientific community by its structural attributes, is a fascinating organic compound with a variety of applications. Here are some notable facts:

  • Chemical Structure: This compound features a unique tetrahydrofuran ring, which is a five-membered cyclic ether. Its structure contributes to its intriguing chemical reactivity.
  • Functional Groups: It contains both a ketone and an ether functional group, making it an interesting subject for studies related to organic synthesis.
  • Role in Synthesis: 3-Ethyl-3-phenyl-tetrahydrofuran-2-one is often used as a precursor in the synthesis of various pharmaceuticals and agrochemicals, showcasing its importance in medicinal chemistry.
  • Flavors and Fragrances: The compound is noted for its potential applications in the food industry, particularly as a fragrance or flavoring agent due to its aromatic properties.
  • Research Interest: Scientists are continually investigating its biological activities, which may include antimicrobial and anti-inflammatory properties, thus highlighting its significance in pharmaceutical research.

To quote an esteemed chemist in the field: "Exploring the intricate relationships between chemical structure and biological activity is where the magic of chemistry truly lies." This compound is a prime example of how one structure can lead to multiple pathways for discovery and innovation within the realm of chemistry.

In conclusion, 3-ethyl-3-phenyl-tetrahydrofuran-2-one is not just a molecule; it is a gateway to understanding broader chemical principles and unlocking new potentials in science and industry.

Synonyms
alpha-Ethyl-alpha-phenyl-gamma-butyrolactone
4064-16-8
BEFL
BRN 0144400
3-ethyl-3-phenyloxolan-2-one
5-Etylo-5-fenylo-beta-butyrolakton [Polish]
5-Etylo-5-fenylo-beta-butyrolakton
2(3H)-FURANONE, DIHYDRO-3-ETHYL-3-PHENYL-
4-17-00-05003 (Beilstein Handbook Reference)
SCHEMBL16915056
DTXSID30961034