3-Phenylpyridin-2-amine, with the CAS number 87109-10-2, is an organic compound characterized by a pyridine ring substituted with an amino group and a phenyl group. This compound features a pyridine structure, which is a six-membered aromatic ring containing one nitrogen atom, contributing to its basicity and potential for forming hydrogen bonds. The presence of the amino group (-NH2) enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The phenyl group, a benzene ring, adds to the compound's hydrophobic character and can influence its solubility and interaction with biological systems. 3-Phenylpyridin-2-amine may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its structural features suggest potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the substituents, making it a subject of study in organic synthesis and material science.

3-phenylpyridin-2-amine

87109-10-2: 3-Phenylpyridin-2-amine, with the CAS number 87109-10-2, is an organic compound characterized by a pyridine ring substituted with an amino group and a phenyl group. This compound features a pyridine structure, which is a six-membered aromatic ring containing one nitrogen atom, contributing to its basicity and potential for forming hydrogen bonds. The presence of the amino group (-NH2) enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The phenyl group, a benzene ring, adds to the compound's hydrophobic character and can influence its solubility and interaction with biological systems. 3-Phenylpyridin-2-amine may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its structural features suggest potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the substituents, making it a subject of study in organic synthesis and material science.

CAS 87109-10-2

3-phenylpyridin-2-amine

3-Phenylpyridin-2-amine

Ref: IN-DA004TZN

3-Phenyl-pyridin-2-ylamine

Ref: 54-OR903930

3-phenylpyridin-2-ylamine

Ref: 10-F076742