6-Chloro-1-phenyl-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one is a heterocyclic compound characterized by its unique pyrazolo-pyrimidine structure. This compound features a chloro substituent at the 6-position and a phenyl group at the 1-position, contributing to its potential biological activity. The presence of the pyrazolo and pyrimidine rings suggests that it may exhibit properties typical of nitrogen-containing heterocycles, such as the ability to interact with biological targets, including enzymes and receptors. Its molecular structure allows for various functionalization possibilities, making it of interest in medicinal chemistry for the development of pharmaceuticals. The compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its CAS number, 6288-99-9, facilitates its identification in chemical databases and literature. Overall, this compound's unique structural features and potential biological implications make it a subject of interest in research and development within the field of organic and medicinal chemistry.

6-chloro-1-phenyl-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one

6288-99-9: 6-Chloro-1-phenyl-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one is a heterocyclic compound characterized by its unique pyrazolo-pyrimidine structure. This compound features a chloro substituent at the 6-position and a phenyl group at the 1-position, contributing to its potential biological activity. The presence of the pyrazolo and pyrimidine rings suggests that it may exhibit properties typical of nitrogen-containing heterocycles, such as the ability to interact with biological targets, including enzymes and receptors. Its molecular structure allows for various functionalization possibilities, making it of interest in medicinal chemistry for the development of pharmaceuticals. The compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its CAS number, 6288-99-9, facilitates its identification in chemical databases and literature. Overall, this compound's unique structural features and potential biological implications make it a subject of interest in research and development within the field of organic and medicinal chemistry.

CAS 6288-99-9

6-chloro-1-phenyl-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one

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