2-Acetyl-3-chlorothiophene is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features an acetyl group and a chlorine substituent at the 2 and 3 positions of the thiophene ring, respectively. It typically appears as a yellow to brown liquid or solid, depending on its purity and specific conditions. The presence of the acetyl group contributes to its reactivity, making it a potential intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. The chlorine atom enhances its electrophilic character, allowing for further chemical modifications. 2-Acetyl-3-chlorothiophene is soluble in organic solvents, and its properties can be influenced by factors such as temperature and solvent polarity. Safety data should be consulted for handling, as it may pose health risks if inhaled or ingested. Overall, this compound is of interest in various fields, including materials science and medicinal chemistry, due to its unique structural features and reactivity.

2-Acetyl-3-chlorothiophene

89581-82-8: 2-Acetyl-3-chlorothiophene is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features an acetyl group and a chlorine substituent at the 2 and 3 positions of the thiophene ring, respectively. It typically appears as a yellow to brown liquid or solid, depending on its purity and specific conditions. The presence of the acetyl group contributes to its reactivity, making it a potential intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. The chlorine atom enhances its electrophilic character, allowing for further chemical modifications. 2-Acetyl-3-chlorothiophene is soluble in organic solvents, and its properties can be influenced by factors such as temperature and solvent polarity. Safety data should be consulted for handling, as it may pose health risks if inhaled or ingested. Overall, this compound is of interest in various fields, including materials science and medicinal chemistry, due to its unique structural features and reactivity.

CAS 89581-82-8

2-Acetyl-3-chlorothiophene

2-Acetyl-3-chlorothiophene

Ref: IN-DA003GAX

2-Acetyl-3-chlorothiophene

Ref: 54-OR15400

2-Acetyl-3-chlorothiophene

Ref: 10-F217656