Menthofuran

Menthofuran

File:Menthofuran.svg
Names
IUPAC name 3,6-Dimethyl-4,5,6,7-tetrahydro-1-benzofuran
Identifiers
CAS Number	494-90-6 Error creating thumbnail: Y 17957-94-7 (R) Error creating thumbnail: Y 80183-38-6 (S) Error creating thumbnail: Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:50542
ChemSpider	292309
ECHA InfoCard
E number
PubChem CID	329983
UNII	LK024V9U3C Error creating thumbnail: Y 9N0IS8189W (R) Error creating thumbnail: Y OS9602CGD2 (S) Error creating thumbnail: Y
CompTox Dashboard (EPA)	{{#property:P3117}}
InChI InChI=1S/C10H14O/c1-7-3-4-9-8(2)6-11-10(9)5-7/h6-7H,3-5H2,1-2H3 Key: YGWKXXYGDYYFJU-UHFFFAOYSA-N InChI=1/C10H14O/c1-7-3-4-9-8(2)6-11-10(9)5-7/h6-7H,3-5H2,1-2H3 Key: YGWKXXYGDYYFJU-UHFFFAOYAW
SMILES o1c2c(c(c1)C)CCC(C2)C
Properties
Chemical formula	C10H14O
Molar mass	150.221 g·mol−1
Boiling point	208
Hazards
Flash point	86
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Menthofuran is an organic compound found in a variety of essential oils including that of pennyroyal (Mentha pulegium). It is highly toxic and believed to be the primary toxin in pennyroyal responsible for its potentially fatal effects. After ingestion of menthofuran, it is metabolically activated to chemically reactive intermediates that are hepatotoxic.

Biosynthesis

Menthofuran is produced biosynthetically from pulegone by the enzyme menthofuran synthase.

File:(+)-menthofuran synthase reaction.PNG

Menthofuran synthase converts pulegone to menthofuran

Chemistry

Synthesis

Menthofuran can be synthesized from 5-methylcyclohexane-1,3-dione and allenyldimethylsulfonium bromide in two steps via a furannulation strategy consisting of enolate addition and rearrangement.

Pharmacology

Menthofuran is a metabolite of pulegone. Both in vitro and in vivo studies have found the pulegone metabolite menthofuran to be an inhibitor of CYP2A6.

Menthofuran may deplete glutathione levels, leaving hepatocytes vulnerable to free radical damage.