1-(4-Methoxyphenyl)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione, identified by its CAS number 28921-29-1, is a chemical compound that belongs to the class of thioxodihydropyrimidines. This substance features a pyrimidine ring with two carbonyl groups and a thione (sulfur-containing) functional group, contributing to its unique reactivity and properties. The presence of the 4-methoxyphenyl group enhances its lipophilicity and may influence its biological activity. Typically, compounds of this nature exhibit potential pharmacological properties, including antimicrobial and anti-inflammatory activities, making them of interest in medicinal chemistry. The molecular structure allows for various interactions, including hydrogen bonding and π-π stacking, which can affect solubility and stability. Additionally, the compound may undergo various chemical reactions, such as nucleophilic substitutions or cyclization, depending on the conditions. Overall, this compound's characteristics make it a subject of interest for further research in drug development and synthetic chemistry.

1-(4-methoxyphenyl)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione

28921-29-1: 1-(4-Methoxyphenyl)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione, identified by its CAS number 28921-29-1, is a chemical compound that belongs to the class of thioxodihydropyrimidines. This substance features a pyrimidine ring with two carbonyl groups and a thione (sulfur-containing) functional group, contributing to its unique reactivity and properties. The presence of the 4-methoxyphenyl group enhances its lipophilicity and may influence its biological activity. Typically, compounds of this nature exhibit potential pharmacological properties, including antimicrobial and anti-inflammatory activities, making them of interest in medicinal chemistry. The molecular structure allows for various interactions, including hydrogen bonding and π-π stacking, which can affect solubility and stability. Additionally, the compound may undergo various chemical reactions, such as nucleophilic substitutions or cyclization, depending on the conditions. Overall, this compound's characteristics make it a subject of interest for further research in drug development and synthetic chemistry.

CAS 28921-29-1

1-(4-methoxyphenyl)-2-thioxodihydropyrimidine-4,6(1H,5H)-dione

1-(4-Methoxyphenyl)-2-sulfanylidene-1,3-diazinane-4,6-dione

Ref: 3D-DBA92129