5-(3-Thienyl)pyrimidine is an organic compound characterized by its pyrimidine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms at positions 1 and 3. The presence of a thienyl group, derived from thiophene, at the 5-position of the pyrimidine ring introduces unique electronic and steric properties, making this compound of interest in various fields, including medicinal chemistry and materials science. The thienyl moiety can enhance the compound's solubility and reactivity, potentially influencing its biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its synthesis often involves coupling reactions or other methods to introduce the thienyl group onto the pyrimidine scaffold. Due to its structural features, 5-(3-Thienyl)pyrimidine may interact with biological targets, making it a candidate for further investigation in drug development or as a building block in organic synthesis. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

5-(3-Thienyl)pyrimidine

58759-02-7: 5-(3-Thienyl)pyrimidine is an organic compound characterized by its pyrimidine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms at positions 1 and 3. The presence of a thienyl group, derived from thiophene, at the 5-position of the pyrimidine ring introduces unique electronic and steric properties, making this compound of interest in various fields, including medicinal chemistry and materials science. The thienyl moiety can enhance the compound's solubility and reactivity, potentially influencing its biological activity. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its synthesis often involves coupling reactions or other methods to introduce the thienyl group onto the pyrimidine scaffold. Due to its structural features, 5-(3-Thienyl)pyrimidine may interact with biological targets, making it a candidate for further investigation in drug development or as a building block in organic synthesis. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

CAS 58759-02-7

5-(3-Thienyl)pyrimidine

5-(3-Thienyl)pyrimidine

Ref: 10-F200870