5-(4-Chlorophenyl)-4-hydrazinothieno[2,3-d]pyrimidine is a chemical compound characterized by its unique structural features, which include a thieno[2,3-d]pyrimidine core substituted with a hydrazine group and a 4-chlorophenyl moiety. This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of the hydrazine functional group, which can participate in various chemical reactions. The thieno[2,3-d]pyrimidine framework is known for its role in medicinal chemistry, often serving as a scaffold for the development of pharmaceuticals. The presence of the chlorine atom on the phenyl ring may influence the compound's lipophilicity and biological interactions. Additionally, the compound may exhibit specific solubility characteristics, stability under various conditions, and reactivity patterns typical of hydrazine derivatives. Its potential applications could span across fields such as drug development, agrochemicals, or materials science, depending on its biological activity and chemical reactivity. Further studies would be necessary to elucidate its specific properties and applications.

5-(4-CHLOROPHENYL)-4-HYDRAZINOTHIENO[2,3-D]PYRIMIDINE

330473-50-2: 5-(4-Chlorophenyl)-4-hydrazinothieno[2,3-d]pyrimidine is a chemical compound characterized by its unique structural features, which include a thieno[2,3-d]pyrimidine core substituted with a hydrazine group and a 4-chlorophenyl moiety. This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity due to the presence of the hydrazine functional group, which can participate in various chemical reactions. The thieno[2,3-d]pyrimidine framework is known for its role in medicinal chemistry, often serving as a scaffold for the development of pharmaceuticals. The presence of the chlorine atom on the phenyl ring may influence the compound's lipophilicity and biological interactions. Additionally, the compound may exhibit specific solubility characteristics, stability under various conditions, and reactivity patterns typical of hydrazine derivatives. Its potential applications could span across fields such as drug development, agrochemicals, or materials science, depending on its biological activity and chemical reactivity. Further studies would be necessary to elucidate its specific properties and applications.

CAS 330473-50-2

5-(4-CHLOROPHENYL)-4-HYDRAZINOTHIENO[2,3-D]PYRIMIDINE

5-(4-chlorophenyl)-4-hydrazinylthieno[2,3-d]pyrimidine

Ref: 10-F511662