3-(Thiophen-3-yl)pyridine is an organic compound characterized by the presence of both a pyridine and a thiophene ring in its structure. The pyridine ring is a six-membered aromatic ring containing one nitrogen atom, while the thiophene ring is a five-membered aromatic ring containing one sulfur atom. This compound typically exhibits properties associated with heterocyclic compounds, such as increased reactivity due to the presence of the nitrogen and sulfur atoms. It is generally soluble in organic solvents and may show moderate polarity. The compound can participate in various chemical reactions, including electrophilic substitution and nucleophilic attacks, due to the electron-rich nature of the thiophene and the nitrogen atom in the pyridine. Additionally, 3-(thiophen-3-yl)pyridine may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry and materials science. Its unique structural features contribute to its potential applications in organic electronics, pharmaceuticals, and as a building block in the synthesis of more complex molecules.

3-(thiophen-3-yl)pyridine

21308-81-6: 3-(Thiophen-3-yl)pyridine is an organic compound characterized by the presence of both a pyridine and a thiophene ring in its structure. The pyridine ring is a six-membered aromatic ring containing one nitrogen atom, while the thiophene ring is a five-membered aromatic ring containing one sulfur atom. This compound typically exhibits properties associated with heterocyclic compounds, such as increased reactivity due to the presence of the nitrogen and sulfur atoms. It is generally soluble in organic solvents and may show moderate polarity. The compound can participate in various chemical reactions, including electrophilic substitution and nucleophilic attacks, due to the electron-rich nature of the thiophene and the nitrogen atom in the pyridine. Additionally, 3-(thiophen-3-yl)pyridine may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry and materials science. Its unique structural features contribute to its potential applications in organic electronics, pharmaceuticals, and as a building block in the synthesis of more complex molecules.

CAS 21308-81-6

3-(thiophen-3-yl)pyridine

3-(3-Thienyl)pyridine

Ref: 10-F200869

3-(Thiophen-3-yl)pyridine

Ref: 3D-WAA30881