6-Amino-5-(butylamino)-1-propylpyrimidine-2,4(1H,3H)-dione, with the CAS number 99991-93-2, is a chemical compound that belongs to the class of pyrimidine derivatives. This substance features a pyrimidine ring substituted with amino and butylamino groups, contributing to its potential biological activity. The presence of the amino groups suggests that it may participate in hydrogen bonding and could interact with various biological targets, making it of interest in medicinal chemistry. The propyl and butyl substituents enhance its lipophilicity, which may influence its pharmacokinetic properties, such as absorption and distribution in biological systems. The compound's dione functionality indicates the presence of two carbonyl groups, which can participate in various chemical reactions, including nucleophilic attacks and coordination with metal ions. Overall, the structural characteristics of this compound suggest potential applications in pharmaceuticals, particularly in the development of therapeutic agents targeting specific biological pathways. However, detailed studies on its biological activity and safety profile would be necessary to fully understand its potential uses.

6-amino-5-(butylamino)-1-propylpyrimidine-2,4(1H,3H)-dione

99991-93-2: 6-Amino-5-(butylamino)-1-propylpyrimidine-2,4(1H,3H)-dione, with the CAS number 99991-93-2, is a chemical compound that belongs to the class of pyrimidine derivatives. This substance features a pyrimidine ring substituted with amino and butylamino groups, contributing to its potential biological activity. The presence of the amino groups suggests that it may participate in hydrogen bonding and could interact with various biological targets, making it of interest in medicinal chemistry. The propyl and butyl substituents enhance its lipophilicity, which may influence its pharmacokinetic properties, such as absorption and distribution in biological systems. The compound's dione functionality indicates the presence of two carbonyl groups, which can participate in various chemical reactions, including nucleophilic attacks and coordination with metal ions. Overall, the structural characteristics of this compound suggest potential applications in pharmaceuticals, particularly in the development of therapeutic agents targeting specific biological pathways. However, detailed studies on its biological activity and safety profile would be necessary to fully understand its potential uses.

CAS 99991-93-2

6-amino-5-(butylamino)-1-propylpyrimidine-2,4(1H,3H)-dione

6-Amino-5-(butylamino)-1-propylpyrimidine-2,4(1H,3H)-dione

Ref: IN-DA003VTK

6-Amino-5-(butylamino)-1-propyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

Ref: 3D-ZDA99193