1-(3,4-Dibromothiophen-2-yl)ethanone is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of two bromine substituents at the 3 and 4 positions of the thiophene ring significantly influences its chemical properties, including increased reactivity and potential for electrophilic substitution. The ethanone functional group (ketone) contributes to the compound's overall reactivity, particularly in nucleophilic addition reactions. This compound is likely to exhibit moderate solubility in organic solvents due to its aromatic nature, while its polar ketone group may enhance solubility in polar solvents. The presence of bromine atoms can also impart unique electronic properties, making it of interest in various applications, including organic synthesis and materials science. Additionally, the compound's structure suggests potential biological activity, which may warrant further investigation in medicinal chemistry. Safety data should be consulted due to the presence of bromine, which can pose health risks.

1-(3,4-dibromothiophen-2-yl)ethanone

57681-57-9: 1-(3,4-Dibromothiophen-2-yl)ethanone is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of two bromine substituents at the 3 and 4 positions of the thiophene ring significantly influences its chemical properties, including increased reactivity and potential for electrophilic substitution. The ethanone functional group (ketone) contributes to the compound's overall reactivity, particularly in nucleophilic addition reactions. This compound is likely to exhibit moderate solubility in organic solvents due to its aromatic nature, while its polar ketone group may enhance solubility in polar solvents. The presence of bromine atoms can also impart unique electronic properties, making it of interest in various applications, including organic synthesis and materials science. Additionally, the compound's structure suggests potential biological activity, which may warrant further investigation in medicinal chemistry. Safety data should be consulted due to the presence of bromine, which can pose health risks.

CAS 57681-57-9

1-(3,4-dibromothiophen-2-yl)ethanone

1-(3,4-Dibromo-2-thienyl)-1-ethanone

Ref: IN-DA00EE3E

1-(3,4-Dibromothien-2-yl)ethanone

Ref: 54-OR111072

1-(3,4-dibromothien-2-yl)ethanone

Ref: 10-F519012

1-(3,4-Dibromo-2-thienyl)-1-ethanone

Ref: 3D-HCA68157