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Furfural acetone

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Identification
Molecular formula
C6H6O3
CAS number
1072-83-9
IUPAC name
1-(3-hydroxy-2-furyl)ethanone
State
State

At room temperature, 1-(3-hydroxy-2-furyl)ethanone exists as a liquid.

Melting point (Celsius)
16.50
Melting point (Kelvin)
289.65
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
124.12g/mol
Molar mass
124.1150g/mol
Density
1.2700g/cm3
Appearence

The compound is typically a colorless to pale yellow liquid. It may darken upon prolonged exposure to air and light due to oxidation.

Comment on solubility

Solubility of 1-(3-hydroxy-2-furyl)ethanone

1-(3-hydroxy-2-furyl)ethanone, with its appealing structure and functional groups, shows interesting solubility characteristics. Generally, compounds containing hydroxyl groups and heterocyclic moieties tend to exhibit a good solubility profile in polar solvents, due to their ability to engage in hydrogen bonding.

Key points regarding solubility:

  • Polar solvents: The presence of the hydroxyl group likely enhances solubility in water and alcohols.
  • Non-polar solvents: Solubility in non-polar organic solvents may be limited due to the polar characteristics of the molecule.
  • Temperature effect: Solubility can increase with temperature, which is common for many organic compounds.

In conclusion, 1-(3-hydroxy-2-furyl)ethanone is expected to be moderately soluble in polar environments, ensuring its utility in various chemical applications. Understanding the solubility behavior of such compounds is critical in fields like pharmaceuticals and organic synthesis, where solubility can impact reactivity and bioavailability.

Interesting facts

Interesting Facts About 1-(3-Hydroxy-2-furyl)ethanone

1-(3-Hydroxy-2-furyl)ethanone, often referred to in research and industrial applications, is a fascinating compound with a unique structure and significant chemical properties. Here are some engaging insights into this compound:

  • Natural Occurrence: This compound is a derivative of furfural, which is a compound commonly derived from agricultural by-products, particularly those rich in pentose sugars. This makes 1-(3-hydroxy-2-furyl)ethanone of particular interest in green chemistry.
  • Biological Significance: It has been studied for its potential biological activities, including *antioxidant properties*. Compounds with antioxidant capacities can help reduce oxidative stress in biological systems, making them valuable in pharmaceutical research.
  • Chemical Reactivity: The presence of the hydroxy group (-OH) contributes to its reactivity, allowing it to participate in various chemical reactions, including esterification and condensation. This versatility makes it useful in synthetic organic chemistry.
  • Flavor and Fragrance: It is noted for its potential applications in the food industry, particularly in flavorings and fragrances, where the furyl group contributes to *characteristic aromatic properties*.
  • Research Applications: This compound serves as a valuable intermediate in the synthesis of more complex organic compounds, which can be utilized in various fields such as materials science, agriculture, and medicinal chemistry.

As scientists continue to explore the properties and applications of 1-(3-hydroxy-2-furyl)ethanone, its role in sustainable chemistry and the development of natural products underscores the importance of this remarkable compound.

Synonyms
ISOMALTOL
3420-59-5
1-(3-hydroxyfuran-2-yl)ethanone
Ethanone, 1-(3-hydroxy-2-furanyl)-
2-acetyl-3-hydroxyfuran
Ketone, 3-hydroxy-2-furyl methyl
UNII-76NST80C38
3-hydroxy-2-furyl methyl ketone
76NST80C38
ISOMALTOL [MI]
DTXSID10187790
3-hydroxyfuran-2-yl methyl ketone
DTXCID70110281
hpigcvxmbgowtf-uhfffaoysa-n
1-(3-Hydroxy-2-furyl)ethanone
SCHEMBL27812
88511-92-6
DTXSID301282527
1-(3-Hydroxy-2-furyl)ethanone #
DAA42059
AKOS025296178
2-(1-Hydroxyethylidene)-3(2H)-furanone
HY-126209
F95114
Q2574472