5-Chloropyrimidin-4(3H)-one is a heterocyclic organic compound characterized by a pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a chlorine atom at the 5-position and a carbonyl group at the 4-position contributes to its unique chemical properties. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents. It is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its ability to participate in various chemical reactions, such as nucleophilic substitutions and cyclizations. The compound's reactivity is influenced by the electron-withdrawing nature of the chlorine atom and the carbonyl group, which can affect its acidity and basicity. Additionally, 5-chloropyrimidin-4(3H)-one may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential, as with many chemical substances, to ensure safety and stability.

5-chloropyrimidin-4(3H)-one

4349-08-0: 4-Pyrimidinol, 5-Chloro-, 5-Chloropyrimidin-4-ol

4(1H)-Pyrimidinone, 5-chloro- (9CI)

5-Chloropyrimidin-4-ol

5-Chloropyrimidin-ol is a formamide derivative that has been shown to be an intermediate in the synthesis of various drugs. It is a member of the class of enamines and can be used as a precursor for benzyl, ammonium salt, or chloroacetic acid ester. 5-Chloropyrimidin-ol can also be used as an intermediate to produce cycloalkyl compounds.

CAS 4349-08-0: 5-chloropyrimidin-4(3H)-one

4(1H)-Pyrimidinone, 5-chloro- (9CI)

Ref: IN-DA00DKSE

5-Chloropyrimidin-4-ol

Ref: 54-OR906830

5-Chloropyrimidin-ol

Ref: 3D-FC63485

5-Chloropyrimidin-4-ol

Ref: 10-F077024

5-chloro-3,4-dihydropyrimidin-4-one

Ref: 10-F793330