1H-Indole, 1-acetyl-3-bromo- is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of an acetyl group at the 1-position and a bromo substituent at the 3-position contributes to its reactivity and potential applications in various chemical reactions. This compound typically exhibits moderate solubility in organic solvents, reflecting the hydrophobic nature of the indole framework. It may participate in electrophilic aromatic substitution reactions due to the electron-rich nature of the indole ring, making it a useful intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, the bromine atom can serve as a leaving group or participate in cross-coupling reactions, enhancing its utility in synthetic organic chemistry. The compound's unique structure and functional groups may also impart specific biological activities, making it of interest in medicinal chemistry research. Safety and handling precautions should be observed, as with many halogenated organic compounds, due to potential toxicity and environmental concerns.

1H-Indole, 1-acetyl-3-bromo-

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CAS 66417-73-0: 1H-Indole, 1-acetyl-3-bromo-

1-Acetyl-3-bromoindole

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1-Acetyl-3-bromoindole

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1-Acetyl-3-bromoindole

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1-ACETYL-3-BROMOINDOLE

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