| Weight | 158.2 g/mol |
|---|---|
| Formula | C11H10O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
1-METHOXYNAPHTHALENE (2216-69-5)
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- The selective metalation of 1-methoxynaphthalene in either the 2- or 8-position (Journal of Organometallic Chemistry, 1969)
- Mechanism of 1-Acetyl-2-methoxynaphthalene Isomerisation over a HBEA Zeolite (Journal of Catalysis, 2000)
- The Metalation of 1-Methoxynaphthalene with n-Butyllithium (Journal of Organic Chemistry, 1966)
- Experimental (FT-IR and FT-Raman), electronic structure and DFT studies on 1-methoxynaphthalene. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- Nucleophile / Electrophile Double Additions to (1-Methoxynaphthalene)tricarbonylchromium(0). Application in a Formal Synthesis of the Aklavinone AB Ring (Organometallics, 1991)
- Aromatic Oxidation by Electron Transfer. III.1 Oxidation of 1- and 2-Methoxynaphthalene by Manganic Acetate2 (Journal of the American Chemical Society, 1966)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC=CC2=CC=CC=C21
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InChIKeyNQMUGNMMFTYOHK-UHFFFAOYSA-N
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1-METHOXYNAPHTHALENE
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