1H-Indole-6-acetonitrile, with the CAS number 39689-57-1, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a nitrile functional group (-C≡N) attached to the 6-position of the indole ring, along with an acetonitrile side chain. It is typically a white to off-white solid and is soluble in organic solvents. The presence of the nitrile group contributes to its reactivity, making it useful in various chemical syntheses and applications in medicinal chemistry. 1H-Indole-6-acetonitrile may exhibit biological activity, which has led to interest in its potential as a pharmaceutical intermediate or in agrochemical formulations. Its properties, such as melting point, boiling point, and specific reactivity, can vary based on purity and environmental conditions. As with many indole derivatives, it may also participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, making it a versatile compound in organic synthesis.

1H-Indole-6-acetonitrile

39689-57-1: 1H-Indole-6-acetonitrile, with the CAS number 39689-57-1, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a nitrile functional group (-C≡N) attached to the 6-position of the indole ring, along with an acetonitrile side chain. It is typically a white to off-white solid and is soluble in organic solvents. The presence of the nitrile group contributes to its reactivity, making it useful in various chemical syntheses and applications in medicinal chemistry. 1H-Indole-6-acetonitrile may exhibit biological activity, which has led to interest in its potential as a pharmaceutical intermediate or in agrochemical formulations. Its properties, such as melting point, boiling point, and specific reactivity, can vary based on purity and environmental conditions. As with many indole derivatives, it may also participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, making it a versatile compound in organic synthesis.

CAS 39689-57-1

1H-Indole-6-acetonitrile

1H-Indole,6-acetonitrile

Ref: IN-DA00BXZZ

2-(1h-Indol-6-yl)acetonitrile

Ref: 10-F650850

2-(1H-Indol-6-yl)acetonitrile

Ref: 3D-PBA68957