6,7-Dihydro-5H-pyrrolo[3,4-d]pyrimidine is a bicyclic organic compound characterized by its fused pyrrole and pyrimidine rings. This compound features a nitrogen-containing heterocyclic structure, which contributes to its potential biological activity. It typically appears as a solid at room temperature and is soluble in polar organic solvents. The presence of nitrogen atoms in its structure can influence its reactivity and interactions with biological systems, making it of interest in medicinal chemistry and drug development. The compound may exhibit various pharmacological properties, including potential anti-cancer or anti-inflammatory activities, although specific biological data would depend on empirical studies. Its synthesis often involves multi-step organic reactions, and it can serve as a building block for more complex molecules in pharmaceutical research. As with many heterocycles, it may also participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, depending on the functional groups present. Safety and handling precautions should be observed, as with all chemical substances, particularly in laboratory settings.

6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine

53493-80-4: 6,7-Dihydro-5H-pyrrolo[3,4-d]pyrimidine is a bicyclic organic compound characterized by its fused pyrrole and pyrimidine rings. This compound features a nitrogen-containing heterocyclic structure, which contributes to its potential biological activity. It typically appears as a solid at room temperature and is soluble in polar organic solvents. The presence of nitrogen atoms in its structure can influence its reactivity and interactions with biological systems, making it of interest in medicinal chemistry and drug development. The compound may exhibit various pharmacological properties, including potential anti-cancer or anti-inflammatory activities, although specific biological data would depend on empirical studies. Its synthesis often involves multi-step organic reactions, and it can serve as a building block for more complex molecules in pharmaceutical research. As with many heterocycles, it may also participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, depending on the functional groups present. Safety and handling precautions should be observed, as with all chemical substances, particularly in laboratory settings.

CAS 53493-80-4

6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine

6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine

Ref: IN-DA003N11

6,7-DIHYDRO-5H-PYRROLO[3,4-D]PYRIMIDINE

Ref: 10-F332539