5-(Bromoacetyl)thiophene-2-carbonitrile is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a bromoacetyl group at the 5-position and a cyano group at the 2-position contributes to its reactivity and potential applications in organic synthesis and materials science. This compound typically exhibits properties such as moderate solubility in organic solvents and may participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions, due to the electron-withdrawing nature of the cyano group and the electrophilic bromoacetyl moiety. Its structure allows for potential applications in pharmaceuticals, agrochemicals, and as intermediates in the synthesis of more complex molecules. Additionally, the presence of both electron-withdrawing and electron-donating groups can influence its electronic properties, making it a subject of interest in studies related to electronic materials and sensors. As with many organic compounds, safety precautions should be taken when handling this substance due to its potential toxicity and reactivity.

5-(bromoacetyl)thiophene-2-carbonitrile

496879-84-6: 5-(Bromoacetyl)thiophene-2-carbonitrile is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a bromoacetyl group at the 5-position and a cyano group at the 2-position contributes to its reactivity and potential applications in organic synthesis and materials science. This compound typically exhibits properties such as moderate solubility in organic solvents and may participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions, due to the electron-withdrawing nature of the cyano group and the electrophilic bromoacetyl moiety. Its structure allows for potential applications in pharmaceuticals, agrochemicals, and as intermediates in the synthesis of more complex molecules. Additionally, the presence of both electron-withdrawing and electron-donating groups can influence its electronic properties, making it a subject of interest in studies related to electronic materials and sensors. As with many organic compounds, safety precautions should be taken when handling this substance due to its potential toxicity and reactivity.

CAS 496879-84-6

5-(bromoacetyl)thiophene-2-carbonitrile

5-(Bromoacetyl)thiophene-2-carbonitrile

Ref: IN-DA006YXG

5-(Bromoacetyl)thiophene-2-carbonitrile

Ref: 54-OR30824

5-(Bromoacetyl)thiophene-2-carbonitrile

Ref: 10-F635777