7-Tert-butyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one is a heterocyclic organic compound characterized by its complex fused ring structure, which includes a thieno and pyrimidinone moiety. This compound features a tert-butyl group, contributing to its hydrophobic properties and potentially influencing its biological activity. The presence of multiple rings in its structure suggests that it may exhibit unique electronic properties and steric hindrance, which can affect its reactivity and interactions with biological targets. The compound is likely to be a solid at room temperature, with moderate solubility in organic solvents. Its specific applications may include roles in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the pyrimidinone core, which is often associated with various biological activities. As with many heterocycles, the compound's stability and reactivity can be influenced by the substituents on the rings, making it a subject of interest for further research in synthetic and medicinal chemistry.

7-TERT-BUTYL-5,6,7,8-TETRAHYDRO-3H-BENZO[4,5]THIENO[2,3-D]PYRIMIDIN-4-ONE

380902-66-9: 7-Tert-butyl-5,6,7,8-tetrahydro-3H-benzo[4,5]thieno[2,3-d]pyrimidin-4-one is a heterocyclic organic compound characterized by its complex fused ring structure, which includes a thieno and pyrimidinone moiety. This compound features a tert-butyl group, contributing to its hydrophobic properties and potentially influencing its biological activity. The presence of multiple rings in its structure suggests that it may exhibit unique electronic properties and steric hindrance, which can affect its reactivity and interactions with biological targets. The compound is likely to be a solid at room temperature, with moderate solubility in organic solvents. Its specific applications may include roles in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the pyrimidinone core, which is often associated with various biological activities. As with many heterocycles, the compound's stability and reactivity can be influenced by the substituents on the rings, making it a subject of interest for further research in synthetic and medicinal chemistry.

CAS 380902-66-9

7-TERT-BUTYL-5,6,7,8-TETRAHYDRO-3H-BENZO[4,5]THIENO[2,3-D]PYRIMIDIN-4-ONE

7-tert-Butyl-5,6,7,8-tetrahydro-3H-benzo[4,5]-thieno[2,3-d]pyrimidin-4-one

Ref: 10-F021859