6-(Chloromethyl)-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one is a heterocyclic compound characterized by its pyrazolo-pyrimidine structure, which features a fused ring system containing both pyrazole and pyrimidine moieties. The presence of a chloromethyl group enhances its reactivity, making it a potential intermediate in organic synthesis or a candidate for pharmaceutical applications. This compound typically exhibits moderate to high solubility in polar organic solvents, while its solid-state properties may include crystalline or amorphous forms depending on the synthesis method. The molecular structure suggests potential biological activity, as many pyrazolo-pyrimidine derivatives are known for their roles as kinase inhibitors or in other therapeutic areas. Its molecular weight and specific functional groups contribute to its chemical reactivity, stability, and interaction with biological targets. Safety data should be consulted for handling, as the chloromethyl group can pose hazards. Overall, this compound represents a class of molecules with significant interest in medicinal chemistry and drug development.

6-(chloromethyl)-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one

931075-55-7: 6-(Chloromethyl)-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one is a heterocyclic compound characterized by its pyrazolo-pyrimidine structure, which features a fused ring system containing both pyrazole and pyrimidine moieties. The presence of a chloromethyl group enhances its reactivity, making it a potential intermediate in organic synthesis or a candidate for pharmaceutical applications. This compound typically exhibits moderate to high solubility in polar organic solvents, while its solid-state properties may include crystalline or amorphous forms depending on the synthesis method. The molecular structure suggests potential biological activity, as many pyrazolo-pyrimidine derivatives are known for their roles as kinase inhibitors or in other therapeutic areas. Its molecular weight and specific functional groups contribute to its chemical reactivity, stability, and interaction with biological targets. Safety data should be consulted for handling, as the chloromethyl group can pose hazards. Overall, this compound represents a class of molecules with significant interest in medicinal chemistry and drug development.

CAS 931075-55-7

6-(chloromethyl)-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one

6-(chloromethyl)-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one

Ref: 10-F311202