Lunularin

Lunularin
	File:Lunularin.svg
Names
	Preferred IUPAC name 3-[2-(4-Hydroxyphenyl)ethyl]phenol
Identifiers
CAS Number	37116-80-6;
3D model (JSmol)	Interactive image;
ChemSpider	157893;
ECHA InfoCard	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
E number	Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).
KEGG	C10269;
PubChem CID	181511;
UNII	AXG9EP247C check;
CompTox Dashboard (EPA)	{{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).;
	InChI InChI=1S/C14H14O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-3,6-10,15-16H,4-5H2 Key: ILEYXPCRQKRNIJ-UHFFFAOYSA-N; InChI=1/C14H14O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-3,6-10,15-16H,4-5H2 Key: ILEYXPCRQKRNIJ-UHFFFAOYAQ;
	SMILES c1cc(cc(c1)O)CCc2ccc(cc2)O;
Properties
Chemical formula	C14H14O2
Molar mass	214.26 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Lunularin is a dihydrostilbenoid found in common celery. It has also been found in the roots of Hydrangea macrophylla.^[1]

A lunularic acid decarboxylase has been detected from the liverwort Conocephalum conicum.^[2] It converts lunularic acid into lunularin.

References

^ Lunularic acid and related compounds in liverworts, algae and Hydrangea. John Gorham, Phytochemistry, 1977, Volume 16, Issue 2, Pages 249–253, Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
^ Lunularic acid decarboxylase from the liverwort Conocephalum conicum. Robert J. Pryce and Linda Linton, Phytochemistry, November 1974, Volume 13, Issue 11, Pages 2497–2501, Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).

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

v t e Dihydrostilbenoids and their glycosides
Dihydrostilbenoids	Batatasin-III (3,3′-dihydroxy-5-methoxybibenzyl) Combretastatin and combretastatin B-1 Dihydro-resveratrol Isonotholaenic acid Lunularic acid Lunularin Notholaenic acid Tyrolobibenzyl A, B and C
Oligomeric forms	Bis(bibenzyls): 13,13'-O-Isoproylidenericcardin D Marchantin B and E Neomarchantin A Plagiochin E Riccardin H Macrocyclic bis(benzyls): Marchantin A and C Riccardin B and C Cyclic bibenzyl-dihydrophenanthrene derivative: Cavicularin