3-Acetylbenzothiophene is an organic compound characterized by its unique structure, which consists of a benzothiophene core with an acetyl group attached at the 3-position. This compound typically appears as a yellow to brown solid and is known for its aromatic properties due to the presence of the benzene ring. It exhibits a range of chemical behaviors, including reactivity typical of both aromatic compounds and thiophenes, making it useful in various synthetic applications. The acetyl group contributes to its electrophilic character, allowing it to participate in further chemical reactions, such as Friedel-Crafts acylation or nucleophilic substitutions. Additionally, 3-acetylbenzothiophene may exhibit interesting biological activities, which have drawn attention in medicinal chemistry. Its solubility is generally moderate in organic solvents, and it may show varying degrees of stability under different environmental conditions. Overall, this compound serves as a valuable building block in organic synthesis and materials science.

3-Acetylbenzothiophene

1128-05-8: 1-(1-Benzothiophen-3-Yl)Ethanone, 1-(1-Benzothiophen-3-yl)ethan-1-one, 1-(3-Benzo[b]thienyl)ethanone, 1-(Benzo[b]thien-3-yl)ethanone, 1-(Benzo[b]thiophen-3-yl)ethanone, 1-Benzo[b]thien-3-ylethanone, 3-Acetylbenzo[b]thiophene, 3-Acetylbenzothiophene, 3-Acetylthionaphthene, Ethanone, 1-benzo[b]thien-3-yl-, Ketone, benzo[b]thien-3-yl methyl, NSC 3226

3-acetylbenzo[b]thiophene is an isomeric molecule that has been shown to inhibit the reuptake of dopamine by binding to the dopamine transporter. It has a high affinity for the dopamine transporter, and has been shown to be selective for this receptor. 3-acetylbenzo[b]thiophene is not toxic in mice at doses up to 150 mg/kg, and has a safety profile similar to placebo. This drug can be administered orally, which makes it more convenient than other drugs with similar pharmacokinetic properties (e.g., amphetamine). The optical properties of this compound make it suitable for confocal microscopy. 3-acetylbenzo[b]thiophene also reacts with camphor, a chemical in plants such as cinnamon and bay leaves, with photoexcited fluorescence and chemoenzymatic reactions.

CAS 1128-05-8: 3-Acetylbenzothiophene

3-acetylbenzo[b]thiophene

Ref: 3D-FA35244

1-(1-benzothiophen-3-yl)ethan-1-one

Ref: IN-DA003ISY

1-(Benzo[b]thiophen-3-yl)ethan-1-one

Ref: 10-F620398

3-Acetylthianaphthene

Ref: 54-OR937265