1-(4-Chlorothiophen-3-yl)ethanone, with the CAS number 91387-31-4, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a chlorinated substituent at the para position of the thiophene ring, contributing to its unique chemical properties. The ethanone functional group indicates the presence of a carbonyl group (C=O) adjacent to an ethyl group, which influences its reactivity and potential applications in organic synthesis. The presence of the chlorine atom can enhance the compound's electrophilicity, making it useful in various chemical reactions, including nucleophilic substitutions. Additionally, the thiophene moiety can impart interesting electronic properties, making this compound of interest in materials science and pharmaceuticals. Its solubility and stability in different solvents can vary, depending on the specific conditions and the presence of other functional groups in a given reaction environment. Overall, 1-(4-chlorothiophen-3-yl)ethanone is a versatile compound with potential applications in synthetic organic chemistry.

1-(4-chlorothiophen-3-yl)ethanone

91387-31-4: 1-(4-Chlorothiophen-3-yl)ethanone, with the CAS number 91387-31-4, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a chlorinated substituent at the para position of the thiophene ring, contributing to its unique chemical properties. The ethanone functional group indicates the presence of a carbonyl group (C=O) adjacent to an ethyl group, which influences its reactivity and potential applications in organic synthesis. The presence of the chlorine atom can enhance the compound's electrophilicity, making it useful in various chemical reactions, including nucleophilic substitutions. Additionally, the thiophene moiety can impart interesting electronic properties, making this compound of interest in materials science and pharmaceuticals. Its solubility and stability in different solvents can vary, depending on the specific conditions and the presence of other functional groups in a given reaction environment. Overall, 1-(4-chlorothiophen-3-yl)ethanone is a versatile compound with potential applications in synthetic organic chemistry.

CAS 91387-31-4

1-(4-chlorothiophen-3-yl)ethanone

1-(4-Chlorothiophen-3-yl)ethanone

Ref: IN-DA00GUAW