6-Methoxymellein

6-Methoxymellein
Names
	Preferred IUPAC name 8-Hydroxy-6-methoxy-3-methyl-3,4-dihydro-1H-2-benzopyran-1-one
	Other names 8-Hydroxy-6-methoxy-3-methylisochroman-1-one
Identifiers
CAS Number	13410-15-6 ;
3D model ( JSmol)	Interactive image;
ChemSpider	83993;
PubChem CID	93040;
UNII	424N0263W4 ;
	InChI InChI=1S/C11H12O4/c1-6-3-7-4-8(14-2)5-9(12)10(7)11(13)15-6/h4-6,12H,3H2,1-2H3 Key: AIFNAMVERSBWPS-UHFFFAOYSA-N; InChI=1/C11H12O4/c1-6-3-7-4-8(14-2)5-9(12)10(7)11(13)15-6/h4-6,12H,3H2,1-2H3 Key: AIFNAMVERSBWPS-UHFFFAOYAL;
	SMILES COc1cc(O)c2C(=O)OC(C)Cc2c1;
Properties
Chemical formula	C11H12O4
Molar mass	208.21 g/mol
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

6-Methoxymellein is a

UV-C,^[3] that allows resistance to Botrytis cinerea^[4] and other microorganisms.^[5]

Biosynthesis

6-Methoxymellein is formed from

S-adenosylhomocysteine.^[6]

doi:10.1021/jf990288f

doi:10.1111/j.1439-0434.1993.tb01324.x

doi:10.1016/0885-5765(87)90083-X

doi:10.1016/S0031-9422(00)86959-9

^ "MetaCyc 6-methoxymellein biosynthesis". www.biocyc.org.

External links

6-Methoxymellein on www.biocyc.org

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Types of isocoumarins
Aglycones

Bergenon

Thunberginol A and B

Dihydroisocoumarins

Hydrangenol

Mellein

6-Hydroxymellein

6-Methoxymellein

Monocerin

Phyllodulcin

Thunberginol C, D, E and G

aromatic compound is a stub. You can help Wikipedia by expanding it.
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[1] PMID 12797757

[2] doi:10.1021/jf990288f

[3] doi:10.1111/j.1439-0434.1993.tb01324.x

[4] doi:10.1016/0885-5765(87)90083-X

[5] doi:10.1016/S0031-9422(00)86959-9

[6] "MetaCyc 6-methoxymellein biosynthesis". www.biocyc.org.

[3]

[4]

[5]

[6]

Biosynthesis

References

External links