| Weight | 192.214 g/mol |
|---|---|
| Formula | C11H12O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
5-allyl-2-hydroxy-3-methoxybenzaldehyde (22934-51-6)
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- Synthesis, structural characterization and biological activities of organotin(IV) complexes with 5-allyl-2-hydroxy-3- methoxybenzaldehyde-4-thiosemicarbazone (Journal of Chemical Sciences, 2015)
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SMILESCOC1=C(C(=CC(=C1)CC=C)C=O)O
-
InChIKeyFDHXEIOBIOVBEN-UHFFFAOYSA-N
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Synthesis
Reactant
+
Methyl hydroperoxide
(Dakin oxidation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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67292-69-7
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5-allyl-2-hydroxy-3-methoxybenzaldehyde
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