9-Methyl-2-[(3-nitrobenzyl)sulfanyl]-5H-thiochromeno[4,3-d]pyrimidine is a heterocyclic compound characterized by its complex structure, which includes a thiochromene moiety fused with a pyrimidine ring. The presence of a methyl group and a nitrobenzyl substituent contributes to its unique chemical properties. This compound features a sulfur atom, which is part of a thioether linkage, enhancing its reactivity and potential biological activity. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity and interactions with biological targets. Such compounds often exhibit interesting pharmacological properties, making them subjects of research in medicinal chemistry. The specific arrangement of atoms and functional groups in this molecule can lead to diverse applications, particularly in drug development and synthesis. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions, such as pH and temperature. Overall, 9-methyl-2-[(3-nitrobenzyl)sulfanyl]-5H-thiochromeno[4,3-d]pyrimidine represents a class of compounds with potential utility in various chemical and biological applications.

9-METHYL-2-[(3-NITROBENZYL)SULFANYL]-5H-THIOCHROMENO[4,3-D]PYRIMIDINE

478246-83-2: 9-Methyl-2-[(3-nitrobenzyl)sulfanyl]-5H-thiochromeno[4,3-d]pyrimidine is a heterocyclic compound characterized by its complex structure, which includes a thiochromene moiety fused with a pyrimidine ring. The presence of a methyl group and a nitrobenzyl substituent contributes to its unique chemical properties. This compound features a sulfur atom, which is part of a thioether linkage, enhancing its reactivity and potential biological activity. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity and interactions with biological targets. Such compounds often exhibit interesting pharmacological properties, making them subjects of research in medicinal chemistry. The specific arrangement of atoms and functional groups in this molecule can lead to diverse applications, particularly in drug development and synthesis. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions, such as pH and temperature. Overall, 9-methyl-2-[(3-nitrobenzyl)sulfanyl]-5H-thiochromeno[4,3-d]pyrimidine represents a class of compounds with potential utility in various chemical and biological applications.

CAS 478246-83-2

9-METHYL-2-[(3-NITROBENZYL)SULFANYL]-5H-THIOCHROMENO[4,3-D]PYRIMIDINE