4-Hydroxy-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, with the CAS number 5393-61-3, is an organic compound characterized by its pyrazolone structure, which features a five-membered ring containing two nitrogen atoms. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents, such as ethanol and acetone, but may have limited solubility in water. It possesses functional groups that contribute to its reactivity, including a hydroxyl group and a carbonyl group, which can participate in hydrogen bonding and other chemical interactions. The presence of the phenyl group enhances its aromatic character, potentially influencing its stability and reactivity. This compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential biological activities. Its derivatives may exhibit anti-inflammatory, analgesic, or antimicrobial properties, making it a subject of research in medicinal chemistry. Proper handling and safety measures should be observed, as with any chemical substance, to mitigate any potential hazards associated with its use.

4-hydroxy-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one

5393-61-3: 4-Hydroxy-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one, with the CAS number 5393-61-3, is an organic compound characterized by its pyrazolone structure, which features a five-membered ring containing two nitrogen atoms. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents, such as ethanol and acetone, but may have limited solubility in water. It possesses functional groups that contribute to its reactivity, including a hydroxyl group and a carbonyl group, which can participate in hydrogen bonding and other chemical interactions. The presence of the phenyl group enhances its aromatic character, potentially influencing its stability and reactivity. This compound is of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential biological activities. Its derivatives may exhibit anti-inflammatory, analgesic, or antimicrobial properties, making it a subject of research in medicinal chemistry. Proper handling and safety measures should be observed, as with any chemical substance, to mitigate any potential hazards associated with its use.

CAS 5393-61-3

4-hydroxy-5-methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one

Edaravone Impurity 13

Ref: 4Z-E-5315