METHYL-3-HYDROXY-4-(4-HYROXYBENZYL)-2-NAPHTHOATE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 9KGLy39Q9Hz |
|---|---|
| InChI | InChI=1S/C19H16O4/c1-23-19(22)17-11-13-4-2-3-5-15(13)16(18(17)21)10-12-6-8-14(20)9-7-12/h2-9,11,20-21H,10H2,1H3 |
| InChIKey | LSVVREYRCZOAPC-UHFFFAOYSA-N |
| Mol Weight | 308.33 g/mol |
| Molecular Formula | C19H16O4 |
| Exact Mass | 308.104859 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | ACETONE-D6 |
methyl 4-[(E)-(4-bromophenyl)diazenyl]-3-hydroxy-2-naphthoate
Methyl 4-formyl-3-O-methoxymethyl-2-naphthoate
Methyl 6-tert-butyl-4-formyl-3-hydroxy-2-naphthoate
Calix[4]naphthalene
Ethanone, 1-[4-(2-propenyl)-3-(2-propenyloxy)-2-naphthalenyl]-
3-(bromomethyl)-1-[[3-(bromomethyl)-2-methoxy-1-naphthalenyl]methyl]-2-methoxynaphthalene
Methyl 1-methoxy-2-allyl-3-naphthoate
(2,2-dimethyl-4H-benzo[g][1,3]benzodioxin-10-yl)methanol
Diethyl-2-methylnaphthalene-1,3-dicarboxylate
Methanone, (4-butyl-1-hydroxy-2-naphthalenyl)phenyl-
| Title | Journal or Book | Year |
|---|---|---|
| Tandem Base-Promoted Ring-Opening/Brook Rearrangement/Allylic Alkylation of O-Silyl Cyanohydrins of β-Silyl-α,β-epoxyaldehyde: Scope and Mechanism | The Journal of Organic Chemistry | 2003 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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