| Weight | 148.205 g/mol |
|---|---|
| Formula | C10H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
1,2,3,4-Tetrahydro-1-naphthol (529-33-9, 5929-35-1)
1,2,3,4-tetrahydro-1-naphthalenol
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- Sigma-Aldrich - 1,2,3,4-Tetrahydro-1-naphthol49.10 - 182.50 USD
- Fisher Scientific - Search for 1,2,3,4-Tetrahydro-1-naphthol
- TCI - 1,2,3,4-Tetrahydro-1-naphthol43.00 - 134.00 USD
- Asymmetric synthesis of optically pure (R)()-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol, a key intermediate for optically active anthracyclinone synthesis (Tetrahedron Letters, 1980)
- Use of Cerium(III) Chloride in the Reactions of Carbonyl Compounds with Organolithiums or Grignard Reagents for the Suppression of Abnormal Reactions:1Butyl1,2,3,4Tetrahydro1Naphthol (Organic Syntheses, 2003)
- A novel synthesis of ()-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol, a key intermediate for the synthesis of anthracyclinones (Tetrahedron Letters, 1980)
- A highly enantioselective synthesis of (R)-(-)-2-acetyl-5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol. A key intermediate in the synthesis of anthracyclinones (Tetrahedron Letters, 1991)
- Catalytic Dehydrogenation of Tetralin and 1,2,3,4-Tetrahydro-naphthol-2 in the Liquid Phase (Journal of the American Chemical Society, 1941)
- A short synthesis of + 2-acetyl-5-8-dimethoxy-1,2,3,4-tetrahydro-2-naphthol - a key intermediate for anthracyclinone synthesis (Tetrahedron Letters, 1982)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,2,3,4-tetrahydro-1-naphthalenol
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SMILESC1CC(C2=CC=CC=C2C1)O
-
InChIKeyJAAJQSRLGAYGKZ-UHFFFAOYSA-N
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