2-Methyl-1H-indole-3-carbonitrile, with the CAS number 51072-83-4, is a chemical compound that belongs to the indole family, characterized by its bicyclic structure comprising a fused benzene and pyrrole ring. This compound features a methyl group at the second position and a cyano group (-C≡N) at the third position of the indole ring, which contributes to its unique chemical properties. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the cyano group enhances its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, 2-methyl-1H-indole-3-carbonitrile may display biological activity, which can be explored for potential therapeutic applications. Its structural characteristics and functional groups allow for various chemical reactions, including nucleophilic substitutions and cycloadditions, making it a versatile compound in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

2-methyl-1H-indole-3-carbonitrile

51072-83-4: 2-Methyl-1H-indole-3-carbonitrile, with the CAS number 51072-83-4, is a chemical compound that belongs to the indole family, characterized by its bicyclic structure comprising a fused benzene and pyrrole ring. This compound features a methyl group at the second position and a cyano group (-C≡N) at the third position of the indole ring, which contributes to its unique chemical properties. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the cyano group enhances its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, 2-methyl-1H-indole-3-carbonitrile may display biological activity, which can be explored for potential therapeutic applications. Its structural characteristics and functional groups allow for various chemical reactions, including nucleophilic substitutions and cycloadditions, making it a versatile compound in synthetic organic chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

CAS 51072-83-4

2-methyl-1H-indole-3-carbonitrile

3-Cyano-2-methylindole

Ref: IN-DA00I957

3-Cyano-2-methylindole

Ref: 54-OR912676

2-Methyl-1H-indole-3-carbonitrile

Ref: 10-F092198