5-(3-Pyridyl)thiophen-2-amine is an organic compound characterized by its unique structure, which includes a thiophene ring substituted with an amine group and a pyridine moiety. This compound features a thiophene ring, a five-membered aromatic heterocycle containing sulfur, which contributes to its electronic properties and potential reactivity. The presence of the pyridine ring, a six-membered aromatic ring containing a nitrogen atom, enhances its ability to participate in various chemical interactions, making it of interest in medicinal chemistry and material science. The amine functional group can engage in hydrogen bonding, influencing its solubility and reactivity. This compound may exhibit biological activity, potentially serving as a scaffold for drug development or as a ligand in coordination chemistry. Its specific properties, such as melting point, solubility, and reactivity, would depend on the surrounding conditions and the presence of other functional groups or substituents. Overall, 5-(3-pyridyl)thiophen-2-amine represents a versatile structure with applications in various fields of chemistry.

5-(3-pyridyl)thiophen-2-amine

837376-58-6: 5-(3-Pyridyl)thiophen-2-amine is an organic compound characterized by its unique structure, which includes a thiophene ring substituted with an amine group and a pyridine moiety. This compound features a thiophene ring, a five-membered aromatic heterocycle containing sulfur, which contributes to its electronic properties and potential reactivity. The presence of the pyridine ring, a six-membered aromatic ring containing a nitrogen atom, enhances its ability to participate in various chemical interactions, making it of interest in medicinal chemistry and material science. The amine functional group can engage in hydrogen bonding, influencing its solubility and reactivity. This compound may exhibit biological activity, potentially serving as a scaffold for drug development or as a ligand in coordination chemistry. Its specific properties, such as melting point, solubility, and reactivity, would depend on the surrounding conditions and the presence of other functional groups or substituents. Overall, 5-(3-pyridyl)thiophen-2-amine represents a versatile structure with applications in various fields of chemistry.

CAS 837376-58-6

5-(3-pyridyl)thiophen-2-amine

3-(2-Aminothien-5-yl)pyridine

Ref: 54-OR2148