| Weight | 159.188 g/mol |
|---|---|
| Formula | C10H9NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
3-Acetylindole (703-80-0)
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- Simple N-Alkylation and N-Acylation of 3-Acetylindole and 3-Indolecarbaldehyde (Synthesis, 1987)
- Synthesis of new alkylaminoalkyl thiosemicarbazones of 3-acetylindole and their effect on DNA synthesis and cell proliferation (European Journal of Medicinal Chemistry, 1995)
- REGIOSELECTIVE NITRATION OF 3-ACETYLINDOLE AND ITS N-ACYL AND N-SULFONYL DERIVATIVES (Tetrahedron Letters, 1999)
- The hydrogen bond IR spectra of indole-3-carboxaldehyde and 3-acetylindole crystals The reason behind their similarity (Chemical Physics, 2011)
- Photoinduced [2 + 2] cycloadditions (the PaternoBchi reaction) of 1H-1-acetylindole-2,3-dione with alkenes (Journal of The Chemical Society-perkin Transactions 1, 2001)
- Syntheses of 3-acylindoles via the alkylation of the dianion of 3-acetylindole (Heterocycles, 2002)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(=O)C1=CNC2=CC=CC=C21
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InChIKeyVUIMBZIZZFSQEE-UHFFFAOYSA-N
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