3-Methyl-1-benzothiophene-5-carbonitrile is an organic compound characterized by its unique structure, which includes a benzothiophene core with a methyl group and a cyano group. The presence of the thiophene ring contributes to its aromatic properties, while the cyano group (-C≡N) enhances its reactivity and polarity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in organic synthesis, pharmaceuticals, and materials science, particularly in the development of electronic materials or as intermediates in chemical reactions. The presence of both sulfur and nitrogen in its structure may impart interesting electronic and chemical properties, making it a subject of interest in research. Additionally, the compound's stability and reactivity can be influenced by the substituents on the benzothiophene ring, which can affect its behavior in various chemical environments. Overall, 3-methyl-1-benzothiophene-5-carbonitrile is a versatile compound with potential applications in various fields of chemistry.

3-methyl-1-benzothiophene-5-carbonitrile

19404-23-0: 3-Methyl-1-benzothiophene-5-carbonitrile is an organic compound characterized by its unique structure, which includes a benzothiophene core with a methyl group and a cyano group. The presence of the thiophene ring contributes to its aromatic properties, while the cyano group (-C≡N) enhances its reactivity and polarity. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure suggests potential applications in organic synthesis, pharmaceuticals, and materials science, particularly in the development of electronic materials or as intermediates in chemical reactions. The presence of both sulfur and nitrogen in its structure may impart interesting electronic and chemical properties, making it a subject of interest in research. Additionally, the compound's stability and reactivity can be influenced by the substituents on the benzothiophene ring, which can affect its behavior in various chemical environments. Overall, 3-methyl-1-benzothiophene-5-carbonitrile is a versatile compound with potential applications in various fields of chemistry.

CAS 19404-23-0

3-methyl-1-benzothiophene-5-carbonitrile

3-Methylbenzo[b]thiophene-5-carbonitrile

Ref: IN-DA007RSI

3-Methyl-1-benzothiophene-5-carbonitrile

Ref: 3D-UAA40423