3-Methyl-1,4-diphenyl-1H-pyrazol-5-amine is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features two phenyl groups attached to the 1 and 4 positions of the pyrazole ring, contributing to its aromatic properties and potential for various chemical interactions. The presence of a methyl group at the 3-position enhances its lipophilicity and may influence its biological activity. As an amine, it possesses a primary amine functional group, which can participate in hydrogen bonding and nucleophilic reactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure allows for potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the pyrazole ring, making it a versatile candidate for further research and application in various fields, including pharmaceuticals and agrochemicals.

3-methyl-1,4-diphenyl-1H-pyrazol-5-amine

58314-81-1: 3-Methyl-1,4-diphenyl-1H-pyrazol-5-amine is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features two phenyl groups attached to the 1 and 4 positions of the pyrazole ring, contributing to its aromatic properties and potential for various chemical interactions. The presence of a methyl group at the 3-position enhances its lipophilicity and may influence its biological activity. As an amine, it possesses a primary amine functional group, which can participate in hydrogen bonding and nucleophilic reactions. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure allows for potential applications in drug development, particularly in the design of compounds targeting specific biological pathways. Additionally, the compound's stability, solubility, and reactivity can be influenced by the substituents on the pyrazole ring, making it a versatile candidate for further research and application in various fields, including pharmaceuticals and agrochemicals.

CAS 58314-81-1

3-methyl-1,4-diphenyl-1H-pyrazol-5-amine

3-Methyl-1,4-diphenyl-1H-pyrazol-5-amine

Ref: 3D-ICA31481