2-(5-Ethynylthien-2-yl)pyridine, with the CAS number 132464-90-5, is an organic compound characterized by its unique structural features, which include a pyridine ring and a thienyl group with an ethynyl substituent. This compound typically exhibits properties associated with heterocyclic compounds, such as potential aromaticity due to the presence of nitrogen in the pyridine ring and sulfur in the thienyl moiety. It is likely to be a solid at room temperature, with moderate solubility in organic solvents, reflecting its non-polar characteristics. The presence of the ethynyl group suggests that it may participate in various chemical reactions, including cross-coupling reactions, making it of interest in synthetic organic chemistry. Additionally, compounds of this nature may exhibit biological activity, potentially serving as intermediates in the synthesis of pharmaceuticals or agrochemicals. Its specific reactivity and applications would depend on the functional groups and the overall molecular structure, which can influence its interactions in chemical reactions and biological systems.

2-(5-ETHYNYLTHIEN-2-YL)PYRIDINE

132464-90-5: 2-(5-Ethynylthien-2-yl)pyridine, with the CAS number 132464-90-5, is an organic compound characterized by its unique structural features, which include a pyridine ring and a thienyl group with an ethynyl substituent. This compound typically exhibits properties associated with heterocyclic compounds, such as potential aromaticity due to the presence of nitrogen in the pyridine ring and sulfur in the thienyl moiety. It is likely to be a solid at room temperature, with moderate solubility in organic solvents, reflecting its non-polar characteristics. The presence of the ethynyl group suggests that it may participate in various chemical reactions, including cross-coupling reactions, making it of interest in synthetic organic chemistry. Additionally, compounds of this nature may exhibit biological activity, potentially serving as intermediates in the synthesis of pharmaceuticals or agrochemicals. Its specific reactivity and applications would depend on the functional groups and the overall molecular structure, which can influence its interactions in chemical reactions and biological systems.

CAS 132464-90-5

2-(5-ETHYNYLTHIEN-2-YL)PYRIDINE

Pyridine, 2-(5-ethynyl-2-thienyl)-

Ref: IN-DA0010P3

2-(5-Ethynylthien-2-yl)pyridine

Ref: 54-OR9198

2-(5-Ethynylthiophen-2-yl)pyridine

Ref: 10-F721323