Coniferyl aldehyde

Coniferyl aldehyde
Names
	IUPAC names (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enal; (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enal
	Other names coniferaldehyde; cis-coniferyl aldehyde; trans-coniferyl aldehyde
Identifiers
CAS Number	458-36-6;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:16547;
ChEMBL	ChEMBL242529;
ChemSpider	4444167;
ECHA InfoCard	100.006.618
PubChem CID	5352904; 5280536;
CompTox Dashboard (EPA)	DTXSID8075047 ;
	InChI InChI=1S/C10H10O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-7,12H,1H3/b3-2+;
	SMILES COC1=C(C=CC(=C1)C=CC=O)O;
Properties
Chemical formula	C10H10O3
Molar mass	178.18 g/mol
Density	1.186 g/mL
Melting point	80 °C (176 °F; 353 K)
Boiling point	338.8 °C (641.8 °F; 612.0 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Coniferyl aldehyde is a low molecular weight phenolic compound susceptible to be extracted from cork stoppers into wine.[1]

Metabolism

Dihydroflavonol 4-reductase uses sinapaldehyde or coniferyl aldehyde or coumaraldehyde and NADPH to produce sinapyl alcohol or coniferyl alcohol or coumaryl alcohol respectively and NADP⁺.

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Conde, Elvira; Cadahía, Estrella; García Vallejo, María Concepción; Fernández de Simón, Brígida (1998). "Polyphenolic Composition of Quercus suber Cork from Different Spanish Provenances". J. Agric. Food Chem. 46 (8): 3166–3171. doi:10.1021/jf970863k.

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