5-Amino-1-phenyl-1H-pyrazole-4-carbohydrazide, with the CAS number 58046-54-1, is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group and a phenyl group, contributing to its potential reactivity and biological activity. The carbohydrazide functional group enhances its ability to form hydrogen bonds, making it a candidate for various chemical reactions, including those involving hydrazone formation. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino and hydrazide functionalities. The compound is of interest in medicinal chemistry and may possess pharmacological properties, although specific biological activities would require further investigation. Its synthesis often involves the reaction of hydrazine derivatives with appropriate carbonyl compounds, and it may be utilized in the development of agrochemicals or pharmaceuticals. As with many nitrogen-containing heterocycles, it may also exhibit interesting coordination chemistry with metal ions.

5-amino-1-phenyl-1H-pyrazole-4-carbohydrazide

58046-54-1: 5-Amino-1-phenyl-1H-pyrazole-4-carbohydrazide, with the CAS number 58046-54-1, is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an amino group and a phenyl group, contributing to its potential reactivity and biological activity. The carbohydrazide functional group enhances its ability to form hydrogen bonds, making it a candidate for various chemical reactions, including those involving hydrazone formation. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino and hydrazide functionalities. The compound is of interest in medicinal chemistry and may possess pharmacological properties, although specific biological activities would require further investigation. Its synthesis often involves the reaction of hydrazine derivatives with appropriate carbonyl compounds, and it may be utilized in the development of agrochemicals or pharmaceuticals. As with many nitrogen-containing heterocycles, it may also exhibit interesting coordination chemistry with metal ions.

CAS 58046-54-1

5-amino-1-phenyl-1H-pyrazole-4-carbohydrazide

5-Amino-1-phenyl-1H-pyrazole-4-carbohydrazide

Ref: IN-DA00EDRK

5-Amino-1-phenyl-1H-pyrazole-4-carbohydrazide

Ref: 10-F493969