2-(Propylsulfanyl)pyrimidine-5-carbaldehyde is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. The presence of a propylsulfanyl group at the 2-position introduces a sulfur atom into the molecule, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The aldehyde functional group at the 5-position is indicative of its potential as a reactive intermediate, allowing for further chemical modifications. This compound may exhibit properties such as solubility in organic solvents, and its reactivity can be influenced by the electron-withdrawing nature of the aldehyde and the electron-donating characteristics of the propylsulfanyl group. Its structural features suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. As with many heterocyclic compounds, its biological activity and interactions would depend on the specific functional groups and their spatial arrangement within the molecule.

2-(propylsulfanyl)pyrimidine-5-carbaldehyde

876890-33-4: 2-(Propylsulfanyl)pyrimidine-5-carbaldehyde is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. The presence of a propylsulfanyl group at the 2-position introduces a sulfur atom into the molecule, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The aldehyde functional group at the 5-position is indicative of its potential as a reactive intermediate, allowing for further chemical modifications. This compound may exhibit properties such as solubility in organic solvents, and its reactivity can be influenced by the electron-withdrawing nature of the aldehyde and the electron-donating characteristics of the propylsulfanyl group. Its structural features suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. As with many heterocyclic compounds, its biological activity and interactions would depend on the specific functional groups and their spatial arrangement within the molecule.

2-Propylsulfanyl-pyrimidine-5-carbaldehyde

<p>2-(Propylthio)pyrimidine-5-carbaldehyde (2-PSPCA) is a novel, modified ribonucleoside that has been shown to activate the DNA polymerase. 2-PSPCA has been used in the synthesis of deoxyribonucleosides and phosphoramidites for use in the research and development of antiviral agents and anticancer drugs. 2-PSPCA is a monophosphate with an IC50 of 0.6 mM against human leukemia cells.</p>

CAS 876890-33-4

2-(propylsulfanyl)pyrimidine-5-carbaldehyde

2-Propylsulfanyl-pyrimidine-5-carbaldehyde

Ref: 54-OR916975

2-(Propylthio)pyrimidine-5-carbaldehyde

Ref: 3D-NP57432