2(5H)-Furanone, 4-hydroxy-3-methyl-, also known as 4-hydroxy-3-methyl-2(5H)-furanone, is an organic compound characterized by its furanone structure, which includes a five-membered lactone ring. This compound features a hydroxyl group (-OH) and a methyl group (-CH3) at specific positions on the furanone ring, contributing to its unique chemical properties. It is typically a colorless to pale yellow liquid with a sweet, fruity aroma, often associated with flavors in food and beverages. The compound is soluble in water and organic solvents, making it versatile in various applications, including flavoring agents and fragrances. Its molecular structure allows for potential reactivity in organic synthesis, particularly in the formation of more complex molecules. Additionally, 4-hydroxy-3-methyl-2(5H)-furanone has been studied for its potential biological activities, including antioxidant properties. As with many organic compounds, safety data should be consulted for handling and usage, as it may pose health risks in certain concentrations.

2(5H)-Furanone, 4-hydroxy-3-methyl-

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4-Hydroxy-3-methyl-5h-furan-2-one is a diastereomer of plakortis. It is a natural product that is found in marine sponges. This compound has been shown to have anti-inflammatory properties, which may be due to its inhibition of the glycine receptor. 4-Hydroxy-3-methyl-5h-furan-2-one has also been shown to have a functional theory for its antiplakortis activity, and it has been hypothesized that this may be due to xestospongia.

CAS 516-09-6: 2(5H)-Furanone, 4-hydroxy-3-methyl-

4-Hydroxy-3-methyl-5h-furan-2-one

Ref: 3D-AAA51609

4-HYDROXY-3-METHYL-5H-FURAN-2-ONE

Ref: 10-F468854

4-Hydroxy-3-methyl-5h-furan-2-one

Ref: 54-OR943277

2(5H)-Furanone, 4-hydroxy-3-Methyl-

Ref: IN-DA00DK4Z