5-Bromo-6-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both bromine and methylsulfanyl substituents. The presence of the bromine atom at the 5-position and the methylsulfanyl group at the 2-position contributes to its unique chemical reactivity and potential biological activity. This compound typically exhibits moderate solubility in polar organic solvents due to its polar functional groups, while its aromatic nature may influence its interactions with biological targets. The methyl group at the 6-position can enhance lipophilicity, potentially affecting its pharmacokinetic properties. As a pyrimidinone derivative, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyrimidine derivatives are often associated with diverse biological activities, including antiviral and anticancer properties. Overall, 5-bromo-6-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is a compound of interest for further research in both synthetic and medicinal chemistry.

5-bromo-6-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one

33238-63-0: 5-Bromo-6-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both bromine and methylsulfanyl substituents. The presence of the bromine atom at the 5-position and the methylsulfanyl group at the 2-position contributes to its unique chemical reactivity and potential biological activity. This compound typically exhibits moderate solubility in polar organic solvents due to its polar functional groups, while its aromatic nature may influence its interactions with biological targets. The methyl group at the 6-position can enhance lipophilicity, potentially affecting its pharmacokinetic properties. As a pyrimidinone derivative, it may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions. The compound's structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyrimidine derivatives are often associated with diverse biological activities, including antiviral and anticancer properties. Overall, 5-bromo-6-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is a compound of interest for further research in both synthetic and medicinal chemistry.

CAS 33238-63-0

5-bromo-6-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one

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Ref: IN-DA007GQ8

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