4-Chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine is a heterocyclic compound characterized by its fused pyrazole and pyrimidine rings, which contribute to its unique chemical properties. This compound features a chlorine substituent at the 4-position and a phenyl group at the 1-position of the pyrazolo ring, enhancing its potential for biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the chlorine atom can influence its reactivity and interaction with biological targets, making it of interest in medicinal chemistry. The compound may also display various pharmacological properties, including potential anti-inflammatory or anticancer activities, although specific biological effects would depend on further empirical studies. Its molecular structure allows for diverse synthetic modifications, which can lead to the development of derivatives with tailored properties for specific applications in drug discovery and development. As with many heterocycles, it is important to handle this compound with care, considering safety and environmental regulations.

4-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine

5334-48-5: 4-Chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine is a heterocyclic compound characterized by its fused pyrazole and pyrimidine rings, which contribute to its unique chemical properties. This compound features a chlorine substituent at the 4-position and a phenyl group at the 1-position of the pyrazolo ring, enhancing its potential for biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the chlorine atom can influence its reactivity and interaction with biological targets, making it of interest in medicinal chemistry. The compound may also display various pharmacological properties, including potential anti-inflammatory or anticancer activities, although specific biological effects would depend on further empirical studies. Its molecular structure allows for diverse synthetic modifications, which can lead to the development of derivatives with tailored properties for specific applications in drug discovery and development. As with many heterocycles, it is important to handle this compound with care, considering safety and environmental regulations.

CAS 5334-48-5

4-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine

4-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine

Ref: IN-DA00DG7I

4-Chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine

Ref: 54-OR1053796

4-CHLORO-1-PHENYL-1H-PYRAZOLO[3,4-D]PYRIMIDINE

Ref: 10-F303747