2-Acetyl-5-nitrobenzo[b]furan is an organic compound characterized by its unique structure, which includes a furan ring fused to a benzene ring, along with an acetyl group and a nitro substituent. This compound typically appears as a yellow to orange solid and is known for its potential applications in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The presence of the nitro group contributes to its reactivity, making it a useful building block in the synthesis of more complex molecules. Additionally, the acetyl group can influence the compound's solubility and reactivity, allowing for various chemical transformations. 2-Acetyl-5-nitrobenzo[b]furan may exhibit biological activity, although specific studies on its pharmacological properties may be limited. As with many nitro compounds, it is essential to handle this substance with care due to potential toxicity and environmental concerns. Proper safety measures should be employed when working with this compound in a laboratory setting.

2-Acetyl-5-nitrobenzo[b]furan

23136-39-2: Methyl 5-nitrobenzo[b]furanyl ketone, 1-(5-Nitro-1-Benzofuran-2-Yl)Ethanone

Ethanone, 1-(5-nitro-2-benzofuranyl)-

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CAS 23136-39-2: 2-Acetyl-5-nitrobenzo[b]furan

2-Acetyl-5-nitrobenzo[b]furan

Ref: 10-F013109

Ethanone, 1-(5-nitro-2-benzofuranyl)-

Ref: IN-DA002MBB

2-Acetyl-5-nitrobenzo[b]furan

Ref: 54-OR480704

2-Acetyl-5-nitrobenzo[b]furan

Ref: 3D-FA149659