5-Amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione, also known as a derivative of pyrimidine, is characterized by its unique structure that includes a pyrimidine ring substituted with amino and methyl groups. This compound features two carbonyl groups, contributing to its diketone nature, which plays a significant role in its reactivity and potential applications. The presence of the amino group enhances its solubility in polar solvents and allows for hydrogen bonding, which can influence its biological activity. Typically, compounds of this class are studied for their potential pharmacological properties, including antimicrobial and antitumor activities. The molecular structure also suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or condensation reactions. Its stability and reactivity can be influenced by the presence of substituents on the pyrimidine ring, making it a subject of interest in medicinal chemistry and organic synthesis. Overall, 5-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione is a versatile compound with potential applications in drug development and organic synthesis.

5-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

49738-24-1: 5-Amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione, also known as a derivative of pyrimidine, is characterized by its unique structure that includes a pyrimidine ring substituted with amino and methyl groups. This compound features two carbonyl groups, contributing to its diketone nature, which plays a significant role in its reactivity and potential applications. The presence of the amino group enhances its solubility in polar solvents and allows for hydrogen bonding, which can influence its biological activity. Typically, compounds of this class are studied for their potential pharmacological properties, including antimicrobial and antitumor activities. The molecular structure also suggests that it may participate in various chemical reactions, such as nucleophilic substitutions or condensation reactions. Its stability and reactivity can be influenced by the presence of substituents on the pyrimidine ring, making it a subject of interest in medicinal chemistry and organic synthesis. Overall, 5-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione is a versatile compound with potential applications in drug development and organic synthesis.

CAS 49738-24-1

5-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

5-Amino-1,3-dimethylpyrimidine-2,4(1h,3h)-dione

Ref: IN-DA006YAQ

5-Amino-1,3-dimethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

Ref: 3D-ZBA73824