4-Chloro-2-methyl-6-(1H-pyrazol-1-yl)pyrimidine is a heterocyclic organic compound characterized by its pyrimidine core, which is a six-membered ring containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at the 4-position and a methyl group at the 2-position contributes to its unique chemical properties. Additionally, the substitution of a pyrazole moiety at the 6-position enhances its biological activity and potential applications in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential interactions with biological targets, making it of interest in pharmaceutical research, particularly in the development of agrochemicals or therapeutic agents. The compound's reactivity can be influenced by the electron-withdrawing nature of the chloro group and the electron-donating characteristics of the pyrazole, which may affect its behavior in various chemical reactions. Overall, 4-Chloro-2-methyl-6-(1H-pyrazol-1-yl)pyrimidine is a versatile compound with significant implications in chemical and biological research.

4-Chloro-2-methyl-6(1H-Pyrazol-1-yl)pyrimide

957035-38-0: 4-Chloro-2-methyl-6-(1H-pyrazol-1-yl)pyrimidine is a heterocyclic organic compound characterized by its pyrimidine core, which is a six-membered ring containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at the 4-position and a methyl group at the 2-position contributes to its unique chemical properties. Additionally, the substitution of a pyrazole moiety at the 6-position enhances its biological activity and potential applications in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential interactions with biological targets, making it of interest in pharmaceutical research, particularly in the development of agrochemicals or therapeutic agents. The compound's reactivity can be influenced by the electron-withdrawing nature of the chloro group and the electron-donating characteristics of the pyrazole, which may affect its behavior in various chemical reactions. Overall, 4-Chloro-2-methyl-6-(1H-pyrazol-1-yl)pyrimidine is a versatile compound with significant implications in chemical and biological research.

CAS 957035-38-0

4-Chloro-2-methyl-6(1H-Pyrazol-1-yl)pyrimide

4-Chloro-2-methyl-6-(1H-pyrazol-1-yl)pyrimidine

Ref: IN-DA00H846

4-Chloro-2-methyl-6-(1H-pyrazol-1-yl)pyrimidine

Ref: 54-OR11465

4-Chloro-2-methyl-6-(1H-pyrazol-1-yl)pyrimidine

Ref: 3D-HNB03538