8-Oxogeranial

8-Oxogeranial
Names
	Preferred IUPAC name (2E,6E)-2,6-Dimethylocta-2,6-dienedial
Identifiers
CAS Number	80054-40-6 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:64239;
ChemSpider	9248930;
KEGG	C17622;
PubChem CID	11073781;
CompTox Dashboard (EPA)	DTXSID901032253 ;
	InChI InChI=1S/C10H14O2/c1-9(6-7-11)4-3-5-10(2)8-12/h5-8H,3-4H2,1-2H3/b9-6+,10-5+ Key: GRHWFPUCRVCMRY-TXFIJWAUSA-N; InChI=1/C10H14O2/c1-9(6-7-11)4-3-5-10(2)8-12/h5-8H,3-4H2,1-2H3/b9-6+,10-5+ Key: GRHWFPUCRVCMRY-TXFIJWAUBP;
	SMILES C/C(=C\C=O)/CC/C=C(\C)/C=O;
Properties
Chemical formula	C10H14O2
Molar mass	166.220 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

8-Oxogeranial is a chemical substance (also incorrectly called 10-oxogeranial), that is a monoterpene.^[1] The terpenoid is produced by 8-hydroxygeraniol dehydrogenase which uses 8-hydroxygeraniol as its substrate. 8-Oxogeranial is itself a substrate for iridoid synthase which synthesizes cis-trans-iridodial and cis-trans-nepetalactol.^[2]

References

^ Dewick, Paul M. (2009-02-06). Medicinal Natural Products: A Biosynthetic Approach (1 ed.). Wiley. doi:10.1002/9780470742761. ISBN 978-0-470-74168-9.
^ Miettinen, Karel; Dong, Lemeng; Navrot, Nicolas; Schneider, Thomas; Burlat, Vincent; Pollier, Jacob; Woittiez, Lotte; Van Der Krol, Sander; Lugan, Raphaël; Ilc, Tina; Verpoorte, Robert; Oksman-Caldentey, Kirsi-Marja; Martinoia, Enrico; Bouwmeester, Harro; Goossens, Alain; Memelink, Johan; Werck-Reichhart, Danièle (2014). "The seco-iridoid pathway from Catharanthus roseus". Nature Communications. 5: 3606. doi:10.1038/ncomms4606. PMC 3992524. PMID 24710322.