1-(3-Aminophenyl)-3-phenylurea, with the CAS number 66695-96-3, is an organic compound characterized by its urea functional group, which is linked to both a phenyl and an amino-substituted phenyl group. This compound typically exhibits solid-state properties and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the amino group contributes to its ability to form hydrogen bonds, influencing its solubility and reactivity. Additionally, the phenyl groups provide hydrophobic characteristics, which can affect the compound's interaction with biological membranes. The molecular structure allows for various substitution patterns, which can be explored to enhance its biological activity or modify its physicochemical properties. Overall, 1-(3-aminophenyl)-3-phenylurea serves as a valuable scaffold in drug design, particularly in targeting specific biological pathways or receptors. Its synthesis and characterization are of interest in both academic and industrial research settings.

1-(3-aminophenyl)-3-phenylurea

66695-96-3: 1-(3-Aminophenyl)-3-phenylurea, with the CAS number 66695-96-3, is an organic compound characterized by its urea functional group, which is linked to both a phenyl and an amino-substituted phenyl group. This compound typically exhibits solid-state properties and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the amino group contributes to its ability to form hydrogen bonds, influencing its solubility and reactivity. Additionally, the phenyl groups provide hydrophobic characteristics, which can affect the compound's interaction with biological membranes. The molecular structure allows for various substitution patterns, which can be explored to enhance its biological activity or modify its physicochemical properties. Overall, 1-(3-aminophenyl)-3-phenylurea serves as a valuable scaffold in drug design, particularly in targeting specific biological pathways or receptors. Its synthesis and characterization are of interest in both academic and industrial research settings.

CAS 66695-96-3

1-(3-aminophenyl)-3-phenylurea

3-(3-Aminophenyl)-1-phenylurea

Ref: 3D-RCA69596