4,5,6,7-Tetrahydro-1-benzothiophene-3-carbonitrile is a heterocyclic organic compound characterized by its unique bicyclic structure that incorporates both a thiophene ring and a benzene ring. This compound features a carbonitrile functional group, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The tetrahydro configuration indicates that the compound has four hydrogen atoms added to the benzothiophene framework, resulting in a saturated structure that can influence its physical properties, such as solubility and boiling point. The presence of the carbonitrile group typically imparts polar characteristics, making the compound more soluble in polar solvents. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its specific reactivity and interactions can vary based on the substituents and the overall molecular environment. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic additions and cycloadditions, expanding its utility in synthetic chemistry.

4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile

95461-20-4: 4,5,6,7-Tetrahydro-1-benzothiophene-3-carbonitrile is a heterocyclic organic compound characterized by its unique bicyclic structure that incorporates both a thiophene ring and a benzene ring. This compound features a carbonitrile functional group, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The tetrahydro configuration indicates that the compound has four hydrogen atoms added to the benzothiophene framework, resulting in a saturated structure that can influence its physical properties, such as solubility and boiling point. The presence of the carbonitrile group typically imparts polar characteristics, making the compound more soluble in polar solvents. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its specific reactivity and interactions can vary based on the substituents and the overall molecular environment. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic additions and cycloadditions, expanding its utility in synthetic chemistry.

CAS 95461-20-4

4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile

4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile

Ref: 10-F310951