6-(2-Aminophenyl)-3-(propylsulfanyl)-1,2,4-triazin-5(2H)-one is a chemical compound characterized by its unique triazine core, which is a five-membered heterocyclic ring containing three nitrogen atoms. This compound features an amino group attached to a phenyl ring, contributing to its potential biological activity. The presence of a propylsulfanyl group enhances its chemical reactivity and may influence its solubility and interaction with biological targets. The triazine structure is known for its applications in pharmaceuticals and agrochemicals, often exhibiting diverse biological activities, including antimicrobial and antitumor properties. The compound's molecular structure suggests it may participate in hydrogen bonding due to the amino and carbonyl functionalities, which could be relevant in its interactions with enzymes or receptors. Additionally, the presence of sulfur in the propylsulfanyl group may impart unique electronic properties, making it a subject of interest in medicinal chemistry and material science. Overall, this compound exemplifies the complexity and potential utility of heterocyclic compounds in various chemical and biological applications.

6-(2-aminophenyl)-3-(propylsulfanyl)-1,2,4-triazin-5(2H)-one

419540-20-8: 6-(2-Aminophenyl)-3-(propylsulfanyl)-1,2,4-triazin-5(2H)-one is a chemical compound characterized by its unique triazine core, which is a five-membered heterocyclic ring containing three nitrogen atoms. This compound features an amino group attached to a phenyl ring, contributing to its potential biological activity. The presence of a propylsulfanyl group enhances its chemical reactivity and may influence its solubility and interaction with biological targets. The triazine structure is known for its applications in pharmaceuticals and agrochemicals, often exhibiting diverse biological activities, including antimicrobial and antitumor properties. The compound's molecular structure suggests it may participate in hydrogen bonding due to the amino and carbonyl functionalities, which could be relevant in its interactions with enzymes or receptors. Additionally, the presence of sulfur in the propylsulfanyl group may impart unique electronic properties, making it a subject of interest in medicinal chemistry and material science. Overall, this compound exemplifies the complexity and potential utility of heterocyclic compounds in various chemical and biological applications.

CAS 419540-20-8

6-(2-aminophenyl)-3-(propylsulfanyl)-1,2,4-triazin-5(2H)-one

6-(2-aminophenyl)-3-(propylthio)-1,2,4-triazin-5(4H)-one

Ref: 10-F314471