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Maltol acetate

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Identification
Molecular formula
C9H12O2
CAS number
3508-18-1
IUPAC name
3-allyl-5-methyl-tetrahydrofuran-2-one
State
State

At room temperature, Maltol acetate is typically found in a liquid state. It is an oily liquid owing to its chemical structure and is used in various perfumery and flavoring industries.

Melting point (Celsius)
-27.00
Melting point (Kelvin)
246.15
Boiling point (Celsius)
232.50
Boiling point (Kelvin)
505.65
General information
Molecular weight
156.19g/mol
Molar mass
156.1930g/mol
Density
1.0240g/cm3
Appearence

Maltol acetate appears as a colorless to light yellow liquid with a sweet, fruity odor. Its consistency is typically oily, and it is commonly used in fragrance and flavoring applications due to its aromatic properties.

Comment on solubility

Solubility of 3-allyl-5-methyl-tetrahydrofuran-2-one

3-allyl-5-methyl-tetrahydrofuran-2-one is an organic compound that demonstrates interesting solubility characteristics. Generally, the solubility of a compound can be influenced by several factors, including:

  • Molecular Structure: The presence of functional groups within the molecule can significantly affect solubility. For 3-allyl-5-methyl-tetrahydrofuran-2-one, its tetrahydrofuran moiety often enhances its solubility in organic solvents.
  • Polarity: This compound is expected to have moderate polarity due to its carbonyl group, allowing it to dissolve well in polar organic solvents like ethanol and acetone.
  • Temperature: As with many organic compounds, increasing the temperature can improve solubility, facilitating greater interaction between solvent and solute molecules.
  • Solvent Choice: 3-allyl-5-methyl-tetrahydrofuran-2-one typically exhibits better solubility in organic solvents than in water, which is common with many organic compounds.

In conclusion, while 3-allyl-5-methyl-tetrahydrofuran-2-one may not be water-soluble, it can be effectively dissolved in a range of organic solvents, making it versatile for various applications in organic chemistry and related fields. Understanding the solubility of this compound is essential for its practical applications, including synthesis and formulation.

Interesting facts

Interesting Facts about 3-Allyl-5-Methyl-Tetrahydrofuran-2-One

3-Allyl-5-methyl-tetrahydrofuran-2-one is a remarkable compound that showcases the richness of organic chemistry and the diverse functionalities of cyclic compounds. Here are some captivating insights:

  • Structural Diversity: This compound belongs to the class of tetrahydrofuran derivatives, which are known for their saturated ring structure. This unique configuration provides a high degree of flexibility and reactivity, making it an interesting target for synthetic chemists.
  • Synthetic Versatility: The allyl and methyl substituents on the tetrahydrofuran ring allow for various synthetic modifications, enabling chemists to explore new pathways and create a range of derivatives. This makes it a valuable intermediate in the synthesis of more complex organic molecules.
  • Flavor and Fragrance: Compounds of this type often exhibit pleasant aroma characteristics. This can lead to applications in the food and fragrance industries, where molecules that contribute to specific flavors or scents are prized.
  • Biological Activity: Many tetrahydrofuran derivatives have been studied for their biological activities, including antimicrobial and antifungal properties. While specific studies on 3-allyl-5-methyl-tetrahydrofuran-2-one may be limited, it represents a scaffold that is worth exploring in medicinal chemistry.
  • Cyclization Reactions: The presence of both allyl and carbonyl functionalities can facilitate various cyclization reactions, leading to the formation of new heterocycles, which are often of significant interest in drug discovery.

Overall, 3-allyl-5-methyl-tetrahydrofuran-2-one is not just an ordinary compound; its intriguing structure and potential applications prompt further research and innovation in fields ranging from synthetic organic chemistry to pharmacology.

Synonyms
3926-76-9
2(3H)-FURANONE, 3-ALLYLDIHYDRO-5-METHYL-
4-Allyl-2-methyltetrahydrofuranone-5
3-Allyldihydro-5-methyl-2(3H)-furanone
4-Allilo-2-metylo-tetrahydrofuranonu-5 [Polish]
4-Allilo-2-metylo-tetrahydrofuranonu-5
4-methyl2-allyl-butanolide
SCHEMBL577431
alpha-Allyl-gamma-valerolactone
NIOSH/LU3580900
DTXSID00960014
AKOS015908011
3-allyl-5-methyldihydro-2(3H)-furanone
LU35809000
5-METHYL-3-(PROP-2-EN-1-YL)OXOLAN-2-ONE
4,5-Dihydro-5-methyl-3-(2-propenyl)-2(3H)-furanone
2(3H)-Furanone, 4,5-dihydro-5-methyl-3-(2-propenyl)-