5,6-Dimethylfuro[2,3-d]pyrimidin-4-amine is a heterocyclic organic compound characterized by its fused furan and pyrimidine rings, which contribute to its unique chemical properties. The presence of two methyl groups at the 5 and 6 positions of the furo ring enhances its lipophilicity and may influence its biological activity. This compound typically exhibits moderate solubility in polar solvents due to the presence of the amino group at the 4-position, which can engage in hydrogen bonding. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as compounds with similar frameworks have been explored for their biological activities, including anti-cancer and anti-inflammatory properties. The compound's stability and reactivity can be influenced by the electronic effects of the methyl groups and the amino substituent, making it a subject of interest in synthetic organic chemistry. Overall, 5,6-dimethylfuro[2,3-d]pyrimidin-4-amine represents a versatile scaffold for further chemical modifications and investigations.

5,6-dimethylfuro[2,3-d]pyrimidin-4-amine

5117-94-2: 5,6-Dimethylfuro[2,3-d]pyrimidin-4-amine is a heterocyclic organic compound characterized by its fused furan and pyrimidine rings, which contribute to its unique chemical properties. The presence of two methyl groups at the 5 and 6 positions of the furo ring enhances its lipophilicity and may influence its biological activity. This compound typically exhibits moderate solubility in polar solvents due to the presence of the amino group at the 4-position, which can engage in hydrogen bonding. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as compounds with similar frameworks have been explored for their biological activities, including anti-cancer and anti-inflammatory properties. The compound's stability and reactivity can be influenced by the electronic effects of the methyl groups and the amino substituent, making it a subject of interest in synthetic organic chemistry. Overall, 5,6-dimethylfuro[2,3-d]pyrimidin-4-amine represents a versatile scaffold for further chemical modifications and investigations.

CAS 5117-94-2

5,6-dimethylfuro[2,3-d]pyrimidin-4-amine

5,6-Dimethylfuro[2,3-d]pyrimidin-4-amine

Ref: IN-DA00DVDC

5,6-dimethylfuro[2,3-d]pyrimidin-4-amine

Ref: 10-F314125

5,6-dimethylfuro[2,3-d]pyrimidin-4-amine

Ref: 3D-FAA11794