3H-Pyrazol-3-one, 5-amino- is an organic compound characterized by its pyrazole ring structure, which features a five-membered ring containing two nitrogen atoms. This compound is notable for its amino group (-NH2) at the 5-position of the pyrazole ring, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The presence of the carbonyl group (C=O) at the 3-position contributes to its reactivity, making it a potential candidate for various synthetic applications in medicinal chemistry and material science. Typically, compounds like 3H-Pyrazol-3-one, 5-amino- exhibit properties such as solubility in polar solvents, moderate stability under standard conditions, and the ability to form hydrogen bonds due to the presence of both the amino and carbonyl functional groups. Its unique structure allows for potential applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. As with many nitrogen-containing heterocycles, it may also exhibit biological activity, warranting further investigation into its pharmacological properties.

3H-Pyrazol-3-one, 5-amino-

74586-24-6: 3H-Pyrazol-3-one, 5-amino- is an organic compound characterized by its pyrazole ring structure, which features a five-membered ring containing two nitrogen atoms. This compound is notable for its amino group (-NH2) at the 5-position of the pyrazole ring, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The presence of the carbonyl group (C=O) at the 3-position contributes to its reactivity, making it a potential candidate for various synthetic applications in medicinal chemistry and material science. Typically, compounds like 3H-Pyrazol-3-one, 5-amino- exhibit properties such as solubility in polar solvents, moderate stability under standard conditions, and the ability to form hydrogen bonds due to the presence of both the amino and carbonyl functional groups. Its unique structure allows for potential applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. As with many nitrogen-containing heterocycles, it may also exhibit biological activity, warranting further investigation into its pharmacological properties.

CAS 74586-24-6

3H-Pyrazol-3-one, 5-amino-

5-Amino-3H-pyrazol-3-one

Ref: BD-BD377262