4-Chloro-1H-pyrazole-1-acetonitrile is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. The presence of a chloro substituent at the 4-position of the pyrazole ring and an acetonitrile group at the 1-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow solid and is soluble in polar organic solvents. It exhibits moderate stability under standard conditions but may be sensitive to moisture and light. The presence of the cyano group (acetonitrile) enhances its reactivity, making it useful in various synthetic applications, including the development of agrochemicals and pharmaceuticals. Additionally, the compound may exhibit biological activity, which can be explored in medicinal chemistry. As with many nitrogen-containing heterocycles, it may participate in various chemical reactions, such as nucleophilic substitutions or cycloadditions, making it a versatile intermediate in organic synthesis. Proper handling and storage are essential due to potential toxicity and environmental considerations.

4-Chloro-1H-pyrazole-1-acetonitrile

113336-23-5: 1H-pyrazole-1-acetonitrile, 4-chloro-, 2-(4-Chloro-1H-pyrazol-1-yl)acetonitrile, 2-(4-Chloropyrazol-1-yl)acetonitrile, 4-Chloro-1H-pyrazole-1-acetonitrile, (4-Chloro-1H-pyrazol-1-yl)acetonitrile

(4-Chloro-1H-pyrazol-1-yl)acetonitrile

(4-chloro-1H-pyrazol-1-yl)acetonitrile

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CAS 113336-23-5: 4-Chloro-1H-pyrazole-1-acetonitrile

(4-Chloro-1H-pyrazol-1-yl)acetonitrile

Ref: 54-OR918079

(4-chloro-1H-pyrazol-1-yl)acetonitrile

Ref: 10-F311514

(4-chloro-1H-pyrazol-1-yl)acetonitrile

Ref: IN-DA0081YZ

(4-Chloro-1H-pyrazol-1-yl)acetonitrile

Ref: 3D-FC116054