| Weight | 147.177 g/mol |
|---|---|
| Formula | C9H9NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-Hydroxy-2-methylindole (35320-67-3)
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- Nuclear Magnetic Resonance Spectroscopic Study on the Structure of Two Stereoisomeric Oxygenated Dimers of 3-Methylindole, 5a (H), 11a (H)-12-Hydroxy-10b, 12-dimethyl-5a, 10b, 11a, 12-tetrahydro-6H-oxazolo-[3, 2-a : 4, 5-b'] diindole (Chemical & Pharmaceutical Bulletin, 1985)
- Isolation of a Novel Oxygenated Dimer of 3-Methylindole, 5a (H), 11a (H)-12-Hydroxy-10b, 12-dimethyl-5a, 10b, 11a, 12-tetrahydro-6H-oxazolo-[3, 2-a : 4, 5-b'] diindole, and Structure Determination of Its Acetylated Derivative (Chemical & Pharmaceutical Bulletin, 1985)
- Synthesis of biologically active 1'-(2-oxo-2H-benzopyran-6-yl)- 5'-hydroxy-2'-methylindole-3'-amido-2"-phenyl-thiazolidene-4"-ones. (Acta Poloniae Pharmaceutica, 2011)
- ChemInform Abstract: Condensation of 2Methylindole/Juglone. Synthesis of the First 3,8 Diindolyl5hydroxy1,4naphthoquinone. (ChemInform, 2010)
- ChemInform Abstract: Condensation of 2-Hydroxy-1,4-naphthoquinone/1-Methylindole. Synthesis of a gem-Bisindolylnaphthalene. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC1=CC2=C(N1)C=CC=C2O
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InChIKeyXBVSGEGNQZAQPM-UHFFFAOYSA-N
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