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Sideretin
Names
	IUPAC name 5,7,8-Trihydroxy-6-methoxy-2H-chromen-2-one
	Other names 5,7,8-Trihydroxy-5-methoxycoumarin; 5-Hydroxyfraxetin;
Identifiers
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:5169;
ChemSpider	4437972;
EC Number	209-376-2;
KEGG	C09265;
PubChem CID	125303145;
UNII	CD3GD44O3K ;
	InChI InChI=1S/C10H8O5/c1-14-6-4-5-2-3-7(11)15-10(5)9(13)8(6)12/h2-4,12-13H,1H3 Key: HAVWRBANWNTOJX-UHFFFAOYSA-N; InChI=1/C10H8O5/c1-14-6-4-5-2-3-7(11)15-10(5)9(13)8(6)12/h2-4,12-13H,1H3 Key: HAVWRBANWNTOJX-UHFFFAOYAM;
	SMILES COC1=C(C(=C2C(=C1O)C=CC(=O)O2)O)O;
Properties
Chemical formula	C10H8O6
Molar mass	224.168 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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Sideretin is a catecholic coumarin exuded by numerous dicots into the soil in response to iron deficiency. (CITE - Rajniak et al). Its primary biological role is to reduce ferric iron into the more soluble ferrous form, which can then be readily absorbed by the roots. (CITE - Giehl)

References

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