3-Hydroxybenzaldehyde
Names | |
---|---|
IUPAC name
3-Hydroxybenzaldehyde | |
Other names
m-Hydroxybenzaldehyde; m-Formylphenol; 3-Formylphenol | |
Identifiers | |
100-83-4 | |
ChEBI | CHEBI:16207 |
ChEMBL | ChEMBL243816 |
ChemSpider | 21105795 |
| |
Jmol-3D images | Image |
KEGG | C03067 |
PubChem | 101 |
| |
Properties | |
Molecular formula |
C7H6O2 |
Molar mass | 122.12 g·mol−1 |
Appearance | light-tan crystals |
Melting point | 100 to 103 °C (212 to 217 °F; 373 to 376 K) |
Boiling point | 191 °C (376 °F; 464 K) (50 mmHg) |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
Infobox references | |
3-Hydroxybenzaldehyde is one of the three isomers of hydroxybenzaldehyde.
Chemistry
It has been prepared from 3-nitrobenzaldehyde in a sequence of nitro group reduction, diazotization of the amine, and hydrolysis.[1][2]
Metabolism
3-hydroxybenzyl-alcohol dehydrogenase is an enzyme that uses 3-hydroxybenzyl alcohol and NADP+ to produce 3-hydroxybenzaldehyde, NADPH and H+.
See also
- Salicylaldehyde (2-hydroxybenzaldehyde)
- 4-Hydroxybenzaldehyde
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)