| Weight | 186.21 g/mol |
|---|---|
| Formula | C12H10O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Methyl 2-naphthoate (2459-25-8)
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- Photoinduced proton transfers in methyl salicylate and methyl 2-hydroxy-3-naphthoate (The Journal of Physical Chemistry, 1994)
- Enantioselective oxidative coupling of methyl 3-hydroxy-2-naphthoate using mono-N-alkylated octahydrobinaphthyl-2,2-diamine ligand (Tetrahedron, 2004)
- Molecular Mechanics Study of the Inclusion Complexes of 2-Methyl Naphthoate with - and -Cyclodextrins (Journal of Colloid and Interface Science, 1997)
- -Cyclodextrin-Directed Enantioselective Photocyclodimerization of Methyl 3-Methoxyl-2-naphthoate (Journal of Organic Chemistry, 2009)
- Glucuronidation Converting Methyl 1-(3,4-Dimethoxyphenyl)-3-(3-ethylvaleryl)-4-hydroxy-6,7,8-trimethoxy-2-naphthoate (S-8921) to a Potent Apical Sodium-Dependent Bile Acid Transporter Inhibitor, Resulting in a Hypocholesterolemic Action (Journal of Pharmacology and Experimental Therapeutics, 2007)
- Identification of the Transporters Involved in the Hepatobiliary Transport and Intestinal Efflux of Methyl 1-(3,4-Dimethoxyphenyl)-3-(3-ethylvaleryl)-4-hydroxy-6,7,8-trimethoxy-2-naphthoate (S-8921) Glucuronide, a Pharmacologically Active Metabolite of S-8921 (Drug Metabolism and Disposition, 2008)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCOC(=O)C1=CC2=CC=CC=C2C=C1
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InChIKeyIODOXLXFXNATGI-UHFFFAOYSA-N
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