Skip to main content

2-Acetylfuran

ADVERTISEMENT
Identification
Molecular formula
C6H6O2
CAS number
1192-62-7
IUPAC name
1-tetrahydrofuran-2-ylethanone
State
State

At room temperature, 2-Acetylfuran is in a liquid state.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
168.00
Boiling point (Kelvin)
441.15
General information
Molecular weight
110.12g/mol
Molar mass
110.1160g/mol
Density
1.0630g/cm3
Appearence

2-Acetylfuran is a colorless liquid with a faint, sweet odor. It's typically used as a flavoring agent and in organic synthesis.

Comment on solubility

Solubility of 1-tetrahydrofuran-2-ylethanone

1-tetrahydrofuran-2-ylethanone, a compound featuring a tetrahydrofuran ring, exhibits notable solubility characteristics. As an organic compound, its solubility can be influenced by various factors including temperature and solvent properties. Generally, one can expect:

  • Polar Solvents: This compound tends to dissolve well in polar solvents such as water, ethanol, and methanol due to its functional groups that can engage in hydrogen bonding.
  • Non-Polar Solvents: In contrast, it may have limited solubility in non-polar solvents like hexane or benzene, as these do not enhance its solvation.
  • Temperature Dependence: The solubility often increases with temperature, aligning with the principle that solubility is generally higher at elevated temperatures for many organic compounds.

As a point of reference, “Like dissolves like” serves as a good guideline—polar compounds will typically find a match in polar solvents, enhancing their overall solubility. Given the structure of 1-tetrahydrofuran-2-ylethanone, it can be anticipated that its solubility will align with these trends, making it a versatile compound in various chemical environments.

Interesting facts

Interesting Facts about 1-Tetrahydrofuran-2-ylethanone

1-Tetrahydrofuran-2-ylethanone is a fascinating compound in the realm of organic chemistry, and it presents a multitude of interesting characteristics:

  • Structure and Functionality: The incorporation of a tetrahydrofuran ring adds notable cyclic structure to the molecule, enhancing its reactivity and utility in various chemical reactions.
  • Applications: This compound is utilized as an intermediate in the synthesis of pharmaceuticals and other organic compounds, showcasing its importance in drug discovery and development.
  • Reactivity: The presence of both carbonyl (C=O) and ether functional groups lends to the compound's versatility, making it applicable in electrophilic and nucleophilic reactions.
  • Polymer Chemistry: 1-Tetrahydrofuran-2-ylethanone is often studied in the context of polymerization reactions, where it can introduce specific properties to polymer materials.
  • Environmental Interaction: Understanding the behavior of this compound in various environmental conditions is crucial for assessing its ecological impact, especially in waste disposal scenarios.
  • Synthesis Routes: This compound can be synthesized via various methods, including functionalization of tetrahydrofuran derivatives, showcasing the creativity in chemical synthesis.

In summary, 1-tetrahydrofuran-2-ylethanone is not just a simple compound; its structural characteristics, versatile applications, and important role in organic synthesis make it a significant focus of study for both chemists and industry professionals alike. As one expert notably stated, "Understanding the subtleties of such compounds opens the door to innovative solutions in synthesis and application."

Synonyms
25252-64-6
1-(oxolan-2-yl)ethan-1-one
837-252-3
1-(oxolan-2-yl)ethanone
1-tetrahydrofuran-2-ylethanone
Ethanone, 1-(tetrahydro-2-furanyl)-
1-(tetrahydrofuran-2-yl)ethanone
1-(tetrahydro-2-furanyl)-ethanone
1-[(2R)-tetrahydrofuran-2-yl]ethanone
acetyltetrahydrofuran
MFCD21132114
2-acetyltetrahydrofuran
Furan, 2-acetyl, tetrahydro
SCHEMBL2321562
1-(Tetrahydro-2-furanyl)ethanone
ABA25264
(S)-1-(2-Tetrahydrofuryl)ethanone
MFCD18827605
1-(Tetrahydrofuran-2-yl)ethan-1-one
AKOS014543515
SB45725
SB47322
SB75286
AS-40165
DA-07667
SY339371
DB-062811
DB-073777
CS-0450373
EN300-86268