5-Allylpyrimidine-4,6-diol is a heterocyclic organic compound characterized by a pyrimidine ring substituted with an allyl group and hydroxyl groups at the 4 and 6 positions. This compound features a six-membered aromatic ring containing nitrogen atoms, which contributes to its unique chemical properties. The presence of hydroxyl groups indicates that it can participate in hydrogen bonding, enhancing its solubility in polar solvents and influencing its reactivity. The allyl group introduces a site for potential further chemical modifications, making it a versatile intermediate in organic synthesis. Additionally, the compound may exhibit biological activity, as many pyrimidine derivatives are known for their roles in pharmaceuticals and biochemistry. Its molecular structure allows for various interactions, including potential coordination with metal ions or participation in nucleophilic reactions. Overall, 5-allylpyrimidine-4,6-diol is of interest in both synthetic organic chemistry and medicinal chemistry due to its functional groups and structural features.

5-allylpyrimidine-4,6-diol

16019-30-0: 5-Allylpyrimidine-4,6-diol is a heterocyclic organic compound characterized by a pyrimidine ring substituted with an allyl group and hydroxyl groups at the 4 and 6 positions. This compound features a six-membered aromatic ring containing nitrogen atoms, which contributes to its unique chemical properties. The presence of hydroxyl groups indicates that it can participate in hydrogen bonding, enhancing its solubility in polar solvents and influencing its reactivity. The allyl group introduces a site for potential further chemical modifications, making it a versatile intermediate in organic synthesis. Additionally, the compound may exhibit biological activity, as many pyrimidine derivatives are known for their roles in pharmaceuticals and biochemistry. Its molecular structure allows for various interactions, including potential coordination with metal ions or participation in nucleophilic reactions. Overall, 5-allylpyrimidine-4,6-diol is of interest in both synthetic organic chemistry and medicinal chemistry due to its functional groups and structural features.

CAS 16019-30-0

5-allylpyrimidine-4,6-diol

4(3H)-Pyrimidinone, 6-hydroxy-5-(2-propen-1-yl)-

Ref: IN-DA001RQN

5-Allylpyrimidine-4,6-diol

Ref: 54-OR1051530

5-ALLYLPYRIMIDINE-4,6-DIOL

Ref: 10-F300662