2,5-Dimethoxy-4(3H)-pyrimidinone is an organic compound characterized by its pyrimidine ring structure, which is a six-membered heterocyclic compound containing two nitrogen atoms at positions 1 and 3. This compound features two methoxy groups (-OCH3) attached to the 2 and 5 positions of the pyrimidine ring, contributing to its chemical properties and reactivity. The presence of the carbonyl group (C=O) at the 4-position is significant for its potential biological activity and reactivity in various chemical reactions. Typically, compounds like 2,5-dimethoxy-4(3H)-pyrimidinone may exhibit properties such as solubility in organic solvents, moderate stability under standard conditions, and potential applications in pharmaceuticals or as intermediates in organic synthesis. Its molecular structure suggests that it may participate in hydrogen bonding and other interactions, influencing its behavior in biological systems or chemical reactions. As with many pyrimidine derivatives, it may also exhibit interesting pharmacological properties, warranting further investigation in medicinal chemistry.

2,5-dimethoxy-4(3H)-Pyrimidinone

370103-23-4: 2,5-Dimethoxy-4(3H)-pyrimidinone is an organic compound characterized by its pyrimidine ring structure, which is a six-membered heterocyclic compound containing two nitrogen atoms at positions 1 and 3. This compound features two methoxy groups (-OCH3) attached to the 2 and 5 positions of the pyrimidine ring, contributing to its chemical properties and reactivity. The presence of the carbonyl group (C=O) at the 4-position is significant for its potential biological activity and reactivity in various chemical reactions. Typically, compounds like 2,5-dimethoxy-4(3H)-pyrimidinone may exhibit properties such as solubility in organic solvents, moderate stability under standard conditions, and potential applications in pharmaceuticals or as intermediates in organic synthesis. Its molecular structure suggests that it may participate in hydrogen bonding and other interactions, influencing its behavior in biological systems or chemical reactions. As with many pyrimidine derivatives, it may also exhibit interesting pharmacological properties, warranting further investigation in medicinal chemistry.

CAS 370103-23-4

2,5-dimethoxy-4(3H)-Pyrimidinone

2,5-Dimethoxypyrimidin-4(3H)-one

Ref: 54-OR1064056

Flucytosine Impurity 5

Ref: 4Z-F-428

2,5-DIMETHOXYPYRIMIDIN-4(3H)-ONE

Ref: 10-F835724