3-Hydroxybenzaldehyde

3-Hydroxybenzaldehyde

Names
IUPAC name 3-Hydroxybenzaldehyde
Other names m-Hydroxybenzaldehyde; m-Formylphenol; 3-Formylphenol
Identifiers
CAS Number	100-83-4 Y
3D model (Jmol)	Interactive image
ChEBI	CHEBI:16207 Y
ChEMBL	ChEMBL243816 Y
ChemSpider	21105795 Y
ECHA InfoCard	100.002.630
KEGG	C03067 Y
PubChem	101
UNII	8Z2819J40E Y
InChI InChI=1S/C7H6O2/c8-5-6-2-1-3-7(9)4-6/h1-5,9H Y Key: IAVREABSGIHHMO-UHFFFAOYSA-N Y InChI=1/C7H6O2/c8-5-6-2-1-3-7(9)4-6/h1-5,9H Key: IAVREABSGIHHMO-UHFFFAOYAC
SMILES O=Cc1cc(O)ccc1
Properties
Chemical 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 otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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⁺.

Uses

A known use of 3-Hydroxybenzaldehyde is in the synthesis of Monastrol.

See also

• Salicylaldehyde (2-hydroxybenzaldehyde)
• 4-Hydroxybenzaldehyde

References