5-Chloro-2,4-difluoropyrimidine is a heterocyclic organic compound characterized by its pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of chlorine and fluorine substituents at the 5, 2, and 4 positions, respectively, contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It exhibits moderate polarity due to the electronegative halogen atoms, which can influence its reactivity and solubility in various solvents. 5-Chloro-2,4-difluoropyrimidine is often utilized in pharmaceutical and agrochemical research, serving as an intermediate in the synthesis of biologically active compounds. Its reactivity can be attributed to the presence of the halogen substituents, which can participate in nucleophilic substitution reactions. Additionally, the compound's stability and behavior under different conditions make it a subject of interest in synthetic organic chemistry.

5-Chloro-2,4-difluoropyrimidine

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Pyrimidine, 5-chloro-2,4-difluoro-

5-Chloro-2,4-difluoropyrimidine is a reactive compound that has two hydroxyl groups and a chlorine atom. It reacts with sodium carbonate to form the sodium salt. This reaction is an example of a covalent bond. 5-Chloro-2,4-difluoropyrimidine reacts with chlorine to form the ion pair. This reaction can be amide or sulfate mediated. In the presence of water, 5-chloro-2,4-difluoropyrimidine forms the phenolic compound hydroxylamine. The temperature at which this reaction occurs is important because it affects the rate of reaction and also the product distribution of the reaction.

CAS 25151-07-9: 5-Chloro-2,4-difluoropyrimidine

Pyrimidine, 5-chloro-2,4-difluoro-

Ref: IN-DA002QO1

5-Chloro-2,4-difluoropyrimidine

Ref: 10-F692277

5-Chloro-2,4-difluoropyrimidine

Ref: 54-PC99062

5-Chloro-2,4-Difluoropyrimidine

Ref: 3D-FC79970

5-Chloro-2,4-difluoropyrimidine

Ref: TR-C365805