7-Hydroxy-5-methyl-2H-chromen-2-one, commonly known as 7-hydroxyflavone, is a flavonoid compound characterized by its chromone structure, which consists of a benzopyran ring system. This compound features a hydroxyl group at the 7-position and a methyl group at the 5-position of the chromone ring. It is typically a yellow to orange crystalline solid, exhibiting solubility in organic solvents such as ethanol and methanol, but limited solubility in water. 7-Hydroxyflavone is known for its antioxidant properties and potential health benefits, including anti-inflammatory and neuroprotective effects. It has been studied for its role in various biological activities, including its ability to modulate enzyme activity and interact with cellular signaling pathways. Additionally, this compound may serve as a useful scaffold in the development of pharmaceuticals and nutraceuticals. Its chemical stability and reactivity can be influenced by the presence of the hydroxyl and methyl groups, which can participate in various chemical reactions, including oxidation and complexation with metal ions.

7-hydroxy-5-methyl-2H-chromen-2-one

7249-26-5: 7-Hydroxy-5-methyl-2H-chromen-2-one, commonly known as 7-hydroxyflavone, is a flavonoid compound characterized by its chromone structure, which consists of a benzopyran ring system. This compound features a hydroxyl group at the 7-position and a methyl group at the 5-position of the chromone ring. It is typically a yellow to orange crystalline solid, exhibiting solubility in organic solvents such as ethanol and methanol, but limited solubility in water. 7-Hydroxyflavone is known for its antioxidant properties and potential health benefits, including anti-inflammatory and neuroprotective effects. It has been studied for its role in various biological activities, including its ability to modulate enzyme activity and interact with cellular signaling pathways. Additionally, this compound may serve as a useful scaffold in the development of pharmaceuticals and nutraceuticals. Its chemical stability and reactivity can be influenced by the presence of the hydroxyl and methyl groups, which can participate in various chemical reactions, including oxidation and complexation with metal ions.

CAS 7249-26-5

7-hydroxy-5-methyl-2H-chromen-2-one

5-Methylumbelliferone

Ref: 3B-M2948

7-Hydroxy-5-methyl-2H-chromen-2-one

Ref: 54-OR1066261