5-Amino-1-methyl-1H-pyrazol-3-ol is an organic compound characterized by its pyrazole ring structure, which includes an amino group and a hydroxyl group. This compound typically appears as a white to off-white solid and is soluble in polar solvents due to the presence of the hydroxyl group. It has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, owing to its ability to act as a bioactive molecule. The presence of the amino group can facilitate interactions with biological targets, while the methyl group contributes to its overall hydrophobic character. The compound's reactivity can be influenced by the functional groups attached to the pyrazole ring, making it a versatile intermediate in organic synthesis. Additionally, its stability and solubility characteristics make it suitable for various chemical reactions, including those involving nucleophilic substitutions or coupling reactions. As with many pyrazole derivatives, it may exhibit interesting biological activities, warranting further investigation in drug discovery and development contexts.

5-aMino-1-Methyl-1H-pyrazol-3-ol

857985-10-5: 5-Amino-1-methyl-1H-pyrazol-3-ol is an organic compound characterized by its pyrazole ring structure, which includes an amino group and a hydroxyl group. This compound typically appears as a white to off-white solid and is soluble in polar solvents due to the presence of the hydroxyl group. It has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, owing to its ability to act as a bioactive molecule. The presence of the amino group can facilitate interactions with biological targets, while the methyl group contributes to its overall hydrophobic character. The compound's reactivity can be influenced by the functional groups attached to the pyrazole ring, making it a versatile intermediate in organic synthesis. Additionally, its stability and solubility characteristics make it suitable for various chemical reactions, including those involving nucleophilic substitutions or coupling reactions. As with many pyrazole derivatives, it may exhibit interesting biological activities, warranting further investigation in drug discovery and development contexts.

CAS 857985-10-5

5-aMino-1-Methyl-1H-pyrazol-3-ol

5-Amino-1-methyl-1H-pyrazol-3-ol

Ref: IN-DA00IDS1