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4-Hydroxybenzaldehyde
Names


Preferred IUPAC name 4-Hydroxybenzaldehyde
Other names p-Hydroxybenzaldehyde, 4-formylphenol^[1]
Identifiers
CAS Number	123-08-0^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:17597^Y
ChEMBL	ChEMBL14193^Y
ChemSpider	123^Y
DrugBank	DB03560^Y
ECHA InfoCard	100.004.182
KEGG	C00633^Y
PubChem CID	126
UNII	O1738X3Y38^Y
CompTox Dashboard (EPA)
InChI InChI=1S/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H^Y Key: RGHHSNMVTDWUBI-UHFFFAOYSA-N^Y InChI=1/C7H6O2/c8-5-6-1-3-7(9)4-2-6/h1-5,9H Key: RGHHSNMVTDWUBI-UHFFFAOYAN
SMILES O=Cc1ccc(O)cc1
Properties
Chemical formula	C₇H₆O₂
Molar mass	122.123 g·mol⁻¹
Appearance	yellow to tan powder
Density	1.129 g/cm³ (130 °C)^[1]
Melting point	116 °C (241 °F; 389 K)^[1]
Boiling point	310 to 311 °C (590 to 592 °F; 583 to 584 K)
Solubility in water	12.9 g/L^[2]
Acidity (pK_a)	7.61 (25 °C)^[3]
Magnetic susceptibility (χ)	-78.0·10⁻⁶ cm³/mol
Refractive index (n_D)	1.57051 (130 °C)^[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is ^YN ?) Infobox references

4-Hydroxybenzaldehyde (2-hydroxybenzaldehyde) is an organic compound with the formula C₆H₄OH(CHO).^[4]^[5] Along with 2-hydroxybenzaldehyde and 3-hydroxybenzaldehyde, it is one of the three isomers of hydroxybenzaldehyde.

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Synthesis, reactions, uses

4-Hydroxybenzaldehyde is prepared by reaction of phenol with chloroform, which gives isomeric hydroxybenzal chlorides. Hydrolysis of the C-Cl bonds gives the aldehyde.^[5]

4-Hydroxybenzaldehyde is a precursor to 4-hydroxyphenylglycine, a precursor to penicillins. In the Dakin oxidation, 4-hydroxybenzaldehyde reacts with hydrogen peroxide in base to form hydroquinone.

Metabolism and occurrence

p-Hydroxybenzaldehyde dehydrogenase is an enzyme found in carrots (Daucus carota).^[6]

4-Hydroxybenzaldehyde is found in the orchids Gastrodia elata,^[7] Galeola faberi,^[8] and the Vanilla orchids.

References

^ ^a ^b ^c ^d Haynes, p. 3.304
^ Haynes, p. 5.154
^ Haynes, p. 5.92
^ Merck Index, 11th Edition, 8295
^ ^a ^b Maliverney, Christian; Mulhauser, Michel (2000). "Hydroxybenzaldehydes". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.0825041813011209.a01. ISBN 978-0-471-48494-3.
^ Sircar, D.; Mitra, A. (2008). "Evidence for p-hydroxybenzoate formation involving enzymatic phenylpropanoid side-chain cleavage in hairy roots of Daucus carota". Journal of Plant Physiology. 165 (4): 407–414. doi:10.1016/j.jplph.2007.05.005. PMID 17658659.
^ Ha, J. H.; Lee, D. U.; Lee, J. T.; Kim, J. S.; Yong, C. S.; Kim, J. A.; Ha, J. S.; Huh, K. (2000). "4-Hydroxybenzaldehyde from Gastrodia elata B1. Is active in the antioxidation and GABAergic neuromodulation of the rat brain". Journal of Ethnopharmacology. 73 (1–2): 329–333. doi:10.1016/S0378-8741(00)00313-5. PMID 11025174.
^ Li, Y. M.; Zhou, Z. L.; Hong, Y. F. (1993). "(title in Chinese)" [Studies on the phenolic derivatives from Galeola faberi Rolfe]. Yao Xue Xue Bao = Acta Pharmaceutica Sinica (in Chinese). 28 (10): 766–771. PMID 8009989.

Cited sources

Haynes, William M., ed. (2016). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press. ISBN 9781498754293.

This page was last edited on 7 March 2024, at 18:12

4-Hydroxybenzaldehyde

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