5-Methylisoxazole-3-carbonitrile is a heterocyclic organic compound characterized by its isoxazole ring, which contains both nitrogen and oxygen atoms. The structure features a methyl group at the 5-position and a cyano group (-C≡N) at the 3-position of the isoxazole ring. This compound is typically a colorless to pale yellow solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. The presence of the cyano group contributes to its reactivity, making it a useful intermediate in organic synthesis. Additionally, 5-methylisoxazole-3-carbonitrile may exhibit various physical properties such as solubility in polar solvents, which can vary based on the specific conditions. Its molecular structure allows for interactions that can lead to diverse chemical behaviors, making it of interest in medicinal chemistry and material science. As with many organic compounds, safety data should be consulted to understand its handling and potential hazards.

5-methylisoxazole-3-carbonitrile

57351-99-2: 5-Methyl-3-isoxazolecarbonitrile

5-Methylisoxazole-3-carbonitrile

5-Methylisoxazole-3-carbonitrile is an intermediate in the synthesis of pyridinium salts. It is prepared by the reaction of 5-methylisoxazole with nitrosyl chloride and hydrogen gas. This compound can be used to synthesize pyridinium salts, which are used in a variety of chemical reactions. 5-Methylisoxazole can also be hydrogenated to form isoxazoles, which are used for x-ray diffraction studies. The structure of this molecule was determined by x-ray diffraction experiments that were carried out on crystals of the compound.

CAS 57351-99-2: 5-methylisoxazole-3-carbonitrile

5-Methylisoxazole-3-carbonitrile

Ref: 54-OR12255

5-Methylisoxazole-3-carbonitrile

Ref: 10-F243202

5-Methylisoxazole-3-carbonitrile

Ref: IN-DA003MW9

5-Methylisoxazole-3-carbonitrile

Ref: 3D-FM140708