2-(Benzylsulfanyl)-4-chloro-6-(diethoxymethyl)pyrimidine is a chemical compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing two nitrogen atoms at positions 1 and 3. The presence of a benzylsulfanyl group introduces a sulfur atom, contributing to the compound's reactivity and potential for forming various derivatives. The chloro substituent at position 4 enhances electrophilic characteristics, making it a useful intermediate in organic synthesis. Additionally, the diethoxymethyl group at position 6 provides a hydrophobic character and can influence solubility and biological activity. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its unique structure allows for potential interactions with biological targets, and its synthesis may involve standard organic reactions such as nucleophilic substitutions and coupling reactions. Overall, the combination of functional groups in this compound suggests versatility in applications ranging from pharmaceuticals to agrochemicals.

2-(benzylsulfanyl)-4-chloro-6-(diethoxymethyl)pyrimidine

525559-14-2: 2-(Benzylsulfanyl)-4-chloro-6-(diethoxymethyl)pyrimidine is a chemical compound characterized by its pyrimidine core, which is a six-membered heterocyclic ring containing two nitrogen atoms at positions 1 and 3. The presence of a benzylsulfanyl group introduces a sulfur atom, contributing to the compound's reactivity and potential for forming various derivatives. The chloro substituent at position 4 enhances electrophilic characteristics, making it a useful intermediate in organic synthesis. Additionally, the diethoxymethyl group at position 6 provides a hydrophobic character and can influence solubility and biological activity. This compound may exhibit interesting pharmacological properties, making it a candidate for further research in medicinal chemistry. Its unique structure allows for potential interactions with biological targets, and its synthesis may involve standard organic reactions such as nucleophilic substitutions and coupling reactions. Overall, the combination of functional groups in this compound suggests versatility in applications ranging from pharmaceuticals to agrochemicals.

CAS 525559-14-2

2-(benzylsulfanyl)-4-chloro-6-(diethoxymethyl)pyrimidine

2-Benzylsulfanyl-4-chloro-6-diethoxymethylpyrimidine

Ref: 54-OR75367

2-Benzylsulfanyl-4-chloro-6-diethoxymethyl-pyrimidine

Ref: 10-F317643