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m-Coumaric acid
Names
	Preferred IUPAC name (2E)-3-(3-Hydroxyphenyl)prop-2-enoic acid
	Other names meta-Coumaric acid; 3-Hydroxycinnamic acid
Identifiers
CAS Number	588-30-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:32357;
ChemSpider	553147;
ECHA InfoCard	100.008.742
EC Number	209-615-0;
KEGG	C12621;
PubChem CID	637541;
UNII	KWJ2DDJ34H ;
CompTox Dashboard (EPA)	DTXSID001336224 DTXSID00891551, DTXSID001336224 ;
	InChI InChI=1S/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+ Key: KKSDGJDHHZEWEP-SNAWJCMRSA-N; InChI=1/C9H8O3/c10-8-3-1-2-7(6-8)4-5-9(11)12/h1-6,10H,(H,11,12)/b5-4+ Key: KKSDGJDHHZEWEP-SNAWJCMRBO;
	SMILES C1=CC(=CC(=C1)O)/C=C/C(=O)O;
Properties
Chemical formula	C9H8O3
Molar mass	164.16 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

m-Coumaric acid is a hydroxycinnamic acid, an organic compound that is a hydroxy derivative of cinnamic acid.^[1] There are three isomers of coumaric acid – o-coumaric acid, m-coumaric acid, and p-coumaric acid – that differ by the position of the hydroxy substitution of the phenyl group.

m-Coumaric acid can be found in vinegar.

References

^ m-Coumaric acid at www.phenol-explorer.eu

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

[1] -Coumaric acid at www.phenol-explorer.eu

[1]

M-Coumaric acid

References