| Weight | 158.2 g/mol |
|---|---|
| Formula | C11H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
1-NAPHTHALENEMETHANOL (4780-79-4)
1-naphthylmethanol
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- Disaccharide uptake and priming in animal cells: inhibition of sialyl Lewis X by acetylated Gal beta 1-->4GlcNAc beta-O-naphthalenemethanol. (Proceedings of the National Academy of Sciences of the United States of America, 1995)
- Enantioselective catalysis by 1-(1-isoquinolinyl)-2-naphthalenemethanol: An atropisomerically chiral NO chelating ligand (Tetrahedron-asymmetry, 1994)
- Arylsulfotransferase IV Catalyzed Sulfation of 1-Naphthalenemethanol (Advances in Experimental Medicine and Biology, 1986)
- THE SYNTHESIS OF 1H, 3H-NAPHTHO[1,8-cd]PYRAN-1-ONE, 1,8-DIMETHYL-1, 2,3,4TETRAHYDRONAPHTHALENE, 1,3,3a,4,5,6-HEXAHYDRONAPHTHO[1,8-cd] PYRAN, AND 1,2,3,4-TETRAHYDRO-8-METHYL-1-NAPHTHALENEMETHANOL (Organic Preparations and Procedures International, 1972)
- Solvent-Free Conversion of alpha-Naphthaldehyde to 1-Naphthoic Acid and 1-Naphthalenemethanol: Application of the Cannizzaro Reaction (Journal of Chemical Education, 2004)
- Potential antimalarial compounds in the alpha-(1-dialkyl-aminoethyl)-1-naphthalenemethanol series. (Journal of Organic Chemistry, 1946)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-naphthylmethanol
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SMILESC1=CC=C2C(=C1)C=CC=C2CO
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InChIKeyPBLNHHSDYFYZNC-UHFFFAOYSA-N
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