| Weight | 152.149 g/mol |
|---|---|
| Formula | C8H8O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
5-hydroxy-2-methoxybenzaldehyde (35431-26-6)
35431-26-6
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- Syntheses, spectral, electrochemical and thermal studies of mononuclear manganese(III) complexes with ligands derived from 1,2-propanediamine and 2-hydroxy-3 or 5-methoxybenzaldehyde: self-assembled monolayer formation on nanostructure zinc oxide thin film. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- Selective demethylation of 2,5-dimethoxybenzaldehyde to 5-hydroxy-2-methoxybenzaldehyde (Journal of Organic Chemistry, 1974)
- Synthesis, Crystal Structure, and Electrochemical Properties of Two New Manganese Complexes With a Ligand Derived From 1,2-Propanediamine and 2-Hydroxy-5-Methoxybenzaldehyde (Synthesis and Reactivity in Inorganic Metal-organic and Nano-metal Chemistry, 2013)
- Synthesis, structural characterization, and evaluation of biological activity of organotin(IV) complexes with 2-hydroxy-5-methoxybenzaldehyde-N(4)-methylthiosemicarbazone (Journal of Organometallic Chemistry, 2016)
- (E)-5-((2-Fluorophenyl)diazenyl)-2-hydroxy-3-methoxybenzaldehyde (Acta Crystallographica Section E: Crystallographic Communications, 2005)
- Mechanisms of Antimicrobial Action of Cinnamon and Oregano Oils, Cinnamaldehyde, Carvacrol, 2,5-Dihydroxybenzaldehyde, and 2-Hydroxy-5-Methoxybenzaldehyde against Mycobacterium avium subsp. paratuberculosis (Map) (Foods, 2017)
- 35431-26-6
-
SMILESCOC1=C(C=C(C=C1)O)C=O
-
InChIKeyHWNIBJPEJAWOTR-UHFFFAOYSA-N
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Most-cited Publications
Alternate Names
Estimated Properties
| Boiling Point | 256.12 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 274.3 C | EPI Suite |
| Density | 1.21 g/cm3 | EPA T.E.S.T. |
| Flash Point | 110.63 C | EPA T.E.S.T. |
| Melting Point | 71.55 C | EPI Suite |
| Water Solubility | 2687.1 mg/L | EPA T.E.S.T. |
| Water Solubility | 11030 mg/L | EPI Suite |
External Links
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