3-Hydroxybenzaldehyde
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(Redirected from 3-hydroxybenzaldehyde)
| 3-Hydroxybenzaldehyde | |
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3-Hydroxybenzaldehyde |
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Other names
m-Hydroxybenzaldehyde; m-Formylphenol; 3-Formylphenol |
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| Identifiers | |
| CAS number | 100-83-4 |
| PubChem | 101 |
| ChemSpider | 21105795 |
| KEGG | C03067 |
| ChEBI | CHEBI:16207 |
| ChEMBL | CHEMBL243816 |
| Jmol-3D images | Image 1 |
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| Properties | |
| Molecular formula | C7H6O2 |
| Molar mass | 122.12 g mol−1 |
| Appearance | light-tan crystals |
| Melting point |
100–103 °C |
| Boiling point |
191 °C (50 mmHg) |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
3-Hydroxybenzaldehyde is one of the three isomers of hydroxybenzaldehyde.
Contents |
[edit] Chemistry
It has been prepared from 3-nitrobenzaldehyde in a sequence of nitro group reduction, diazotization of the amine, and hydrolysis.[1][2]
[edit] Metabolism
3-hydroxybenzyl-alcohol dehydrogenase is an enzyme that uses 3-hydroxybenzyl alcohol and NADP+ to produce 3-hydroxybenzaldehyde, NADPH and H+.
[edit] See also
- Salicylaldehyde (2-hydroxybenzaldehyde)
- 4-Hydroxybenzaldehyde
[edit] References
- ^ m-HYDROXYBENZALDEHYDE, Organic Syntheses, Coll. Vol. 3, p.453 (1955); Vol. 25, p.55 (1945)
- ^ m-METHOXYBENZALDEHYDE, Organic Syntheses, Coll. Vol. 3, p.564 (1955); Vol. 29, p.63 (1949)
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