Paracoumaryl alcohol

Names
Preferred IUPAC name 4-[(1E)-3-Hydroxyprop-1-en-1-yl]phenol
Other names p-coumaryl alcohol, 4-coumaryl alcohol, 4-hydroxycinnamyl alcohol, 4-(3-hydroxy-1-propenyl)phenol
Identifiers
CAS Number	20649-40-5 N
3D model (JSmol)	Interactive image
ChEBI	CHEBI:64555 N
ChEMBL	ChEMBL109034 N
ChemSpider	4444166 N
KEGG	C02646 N
PubChem CID	5280535
UNII	61POZ1QQ11 N
CompTox Dashboard (EPA)	DTXSID50895024
InChI InChI=1S/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+ N Key: PTNLHDGQWUGONS-OWOJBTEDSA-N N InChI=1/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+ Key: PTNLHDGQWUGONS-OWOJBTEDBL
SMILES OC/C=C/c1ccc(O)cc1
Properties
Chemical formula	C9H10O2
Molar mass	150.1745
Appearance	White solid
Melting point	114–116 °C (237–241 °F; 387–389 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Paracoumaryl alcohol is a phytochemical, one of the monolignols. It is a white solid. p-Coumaryl alcohol is a major precursor to lignin or lignans.^[1]

Biosynthesis and occurrence[edit]

It is synthesized via the phenylpropanoid biochemical pathway.

Esters of p-coumaryl alcohol and fatty acids are the basis of epicuticular waxes covering the surfaces of apples.

p-Coumaryl alcohol is an intermediate in biosynthesis of chavicol, stilbenoids, and coumarin.

External links[edit]

• Molecule of the week: p-coumaryl alcohol

References[edit]