4-Phenylfurazanamine is an organic compound characterized by its furazan ring structure, which is a five-membered heterocyclic compound containing two nitrogen atoms and three carbon atoms. This compound features a phenyl group attached to the furazan moiety, contributing to its unique chemical properties. It is typically a solid at room temperature and may exhibit various physical properties such as solubility in organic solvents. The presence of the amino group (-NH2) in its structure suggests potential reactivity, particularly in nucleophilic substitution reactions. 4-Phenylfurazanamine may also display interesting biological activities, making it a subject of interest in medicinal chemistry. Its applications could extend to the development of pharmaceuticals or agrochemicals, although specific uses may vary. As with many nitrogen-containing heterocycles, it may also participate in complexation with metal ions, influencing its behavior in various chemical environments. Safety data should be consulted for handling and storage, as with any chemical substance.

4-Phenylfurazanamine

10349-14-1: 4-Phenylfurazanamine is an organic compound characterized by its furazan ring structure, which is a five-membered heterocyclic compound containing two nitrogen atoms and three carbon atoms. This compound features a phenyl group attached to the furazan moiety, contributing to its unique chemical properties. It is typically a solid at room temperature and may exhibit various physical properties such as solubility in organic solvents. The presence of the amino group (-NH2) in its structure suggests potential reactivity, particularly in nucleophilic substitution reactions. 4-Phenylfurazanamine may also display interesting biological activities, making it a subject of interest in medicinal chemistry. Its applications could extend to the development of pharmaceuticals or agrochemicals, although specific uses may vary. As with many nitrogen-containing heterocycles, it may also participate in complexation with metal ions, influencing its behavior in various chemical environments. Safety data should be consulted for handling and storage, as with any chemical substance.

4-Phenyl-1,2,5-oxadiazol-3-amine is an analog of histamine that acts as a competitive antagonist at the H2 receptor. This compound has been shown to elicit histamine release in guinea pig tissues and to act as a competitive antagonist at the H2 receptor. It also blocks histamine binding to other receptors and has been shown to have antihistaminic properties. 4-Phenyl-1,2,5-oxadiazol-3-amine binds in a similar fashion as cimetidine and ranitidine with high affinity for the H2 receptor and lower affinity for the H1 receptor. This drug has also been shown to inhibit guinea pig ileum contractions and rat vas deferens contractions induced by histamine. The molecular weight of this compound is 169.4 g/mol and its chemical formula is C9H7N3O3. The structural formula is:

CAS 10349-14-1

4-Phenylfurazanamine

4-Phenyl-1,2,5-oxadiazol-3-amine

Ref: 3D-KAA34914