5,6-Diamino-1,3-diethylpyrimidine-2,4(1H,3H)-dione, with the CAS number 52998-22-8, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains two amino groups and two ethyl groups. This compound features a dione functional group, indicating the presence of two carbonyl (C=O) groups within its structure. The amino groups contribute to its potential as a building block in pharmaceuticals and agrochemicals, as they can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. The ethyl substituents enhance its lipophilicity, potentially influencing its solubility and bioavailability. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Its stability, reactivity, and interaction with biological systems can vary based on environmental conditions such as pH and temperature. Overall, 5,6-diamino-1,3-diethylpyrimidine-2,4(1H,3H)-dione is a versatile compound with applications in various fields, including drug development and synthetic chemistry.

5,6-diamino-1,3-diethylpyrimidine-2,4(1H,3H)-dione

52998-22-8: 5,6-Diamino-1,3-diethylpyrimidine-2,4(1H,3H)-dione, with the CAS number 52998-22-8, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains two amino groups and two ethyl groups. This compound features a dione functional group, indicating the presence of two carbonyl (C=O) groups within its structure. The amino groups contribute to its potential as a building block in pharmaceuticals and agrochemicals, as they can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. The ethyl substituents enhance its lipophilicity, potentially influencing its solubility and bioavailability. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Its stability, reactivity, and interaction with biological systems can vary based on environmental conditions such as pH and temperature. Overall, 5,6-diamino-1,3-diethylpyrimidine-2,4(1H,3H)-dione is a versatile compound with applications in various fields, including drug development and synthetic chemistry.

CAS 52998-22-8

5,6-diamino-1,3-diethylpyrimidine-2,4(1H,3H)-dione

5,6-Diamino-1,3-diethylpyrimidine-2,4(1H,3H)-dione

Ref: IN-DA003464

1,3-diethyl-5,6-diaminouracil

Ref: 54-OR311188

1,3-Diethyl-5,6-aminouracil

Ref: 7W-GN6170