7-Aminoquinazoline-2,4(1H,3H)-dione, with the CAS number 59674-85-0, is a heterocyclic organic compound characterized by its quinazoline structure, which features a fused benzene and pyrimidine ring system. This compound contains an amino group at the 7-position and two carbonyl groups at the 2 and 4 positions, contributing to its reactivity and potential biological activity. It is typically a crystalline solid, exhibiting moderate solubility in polar solvents. The presence of the amino group allows for hydrogen bonding, which can influence its interactions in biological systems. This compound has garnered interest in medicinal chemistry due to its potential as a scaffold for developing pharmaceuticals, particularly in the context of targeting specific enzymes or receptors. Its derivatives may exhibit various biological activities, including antimicrobial and anticancer properties. As with many heterocycles, the electronic properties of the nitrogen and carbonyl groups can play a significant role in its chemical behavior and reactivity, making it a subject of interest for further research and application in drug development.

7-aminoquinazoline-2,4(1H,3H)-dione

59674-85-0: 7-Aminoquinazoline-2,4(1H,3H)-dione, with the CAS number 59674-85-0, is a heterocyclic organic compound characterized by its quinazoline structure, which features a fused benzene and pyrimidine ring system. This compound contains an amino group at the 7-position and two carbonyl groups at the 2 and 4 positions, contributing to its reactivity and potential biological activity. It is typically a crystalline solid, exhibiting moderate solubility in polar solvents. The presence of the amino group allows for hydrogen bonding, which can influence its interactions in biological systems. This compound has garnered interest in medicinal chemistry due to its potential as a scaffold for developing pharmaceuticals, particularly in the context of targeting specific enzymes or receptors. Its derivatives may exhibit various biological activities, including antimicrobial and anticancer properties. As with many heterocycles, the electronic properties of the nitrogen and carbonyl groups can play a significant role in its chemical behavior and reactivity, making it a subject of interest for further research and application in drug development.

CAS 59674-85-0

7-aminoquinazoline-2,4(1H,3H)-dione

7-Aminoquinazoline-2,4(1H,3H)-dione

Ref: IN-DA00EIG5

7-Aminoquinazoline-2,4(1H,3H)-dione

Ref: 54-OR91094

7-Aminoquinazoline-2,4(1H,3H)-dione

Ref: 10-F091605