5-(Piperidin-1-ylmethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one, with the CAS number 5424-84-0, is a chemical compound that belongs to the class of thioxo-pyrimidinones. This substance features a pyrimidine ring, which is a six-membered aromatic ring containing nitrogen atoms, and a thioxo group, indicating the presence of a sulfur atom double-bonded to a carbon atom. The piperidinylmethyl substituent suggests that the compound has a piperidine ring, a saturated six-membered ring containing one nitrogen atom, attached to the pyrimidine structure. This compound may exhibit biological activity, potentially serving as a pharmacophore in medicinal chemistry. Its properties include solubility in various organic solvents, and it may participate in hydrogen bonding due to the presence of functional groups. The thioxo and piperidine moieties can influence its reactivity and interaction with biological targets, making it of interest in drug development and synthesis. As with many organic compounds, its stability and reactivity can be affected by environmental conditions such as pH and temperature.

5-(piperidin-1-ylmethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one

5424-84-0: 5-(Piperidin-1-ylmethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one, with the CAS number 5424-84-0, is a chemical compound that belongs to the class of thioxo-pyrimidinones. This substance features a pyrimidine ring, which is a six-membered aromatic ring containing nitrogen atoms, and a thioxo group, indicating the presence of a sulfur atom double-bonded to a carbon atom. The piperidinylmethyl substituent suggests that the compound has a piperidine ring, a saturated six-membered ring containing one nitrogen atom, attached to the pyrimidine structure. This compound may exhibit biological activity, potentially serving as a pharmacophore in medicinal chemistry. Its properties include solubility in various organic solvents, and it may participate in hydrogen bonding due to the presence of functional groups. The thioxo and piperidine moieties can influence its reactivity and interaction with biological targets, making it of interest in drug development and synthesis. As with many organic compounds, its stability and reactivity can be affected by environmental conditions such as pH and temperature.

<p>2,3-Dihydro-5-[(piperidin-1-yl)methyl]-2-thioxopyrimidin-4(1H)-one</p>

CAS 5424-84-0

5-(piperidin-1-ylmethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one

2,3-Dihydro-5-[(piperidin-1-yl)methyl]-2-thioxopyrimidin-4(1H)-one

Ref: 54-OR8550