Geranyl pyrophosphate

Geranyl pyrophosphate
	Skeletal formula
	Ball-and-stick model
Names
	Preferred IUPAC name (2E)-3,7-Dimethylocta-2,6-dien-1-yl trihydrogen diphosphate
Identifiers
CAS Number	763-10-0 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:17211 ;
ChEMBL	ChEMBL41342 ;
ChemSpider	393471 ;
DrugBank	DB02552 ;
IUPHAR/BPS	3051;
MeSH	Geranyl+pyrophosphate
PubChem CID	445995;
CompTox Dashboard (EPA)	DTXSID801315430 ;
	InChI InChI=1S/C10H20O7P2/c1-9(2)5-4-6-10(3)7-8-16-19(14,15)17-18(11,12)13/h5,7H,4,6,8H2,1-3H3,(H,14,15)(H2,11,12,13)/b10-7+ Key: GVVPGTZRZFNKDS-JXMROGBWSA-N ; InChI=1/C10H20O7P2/c1-9(2)5-4-6-10(3)7-8-16-19(14,15)17-18(11,12)13/h5,7H,4,6,8H2,1-3H3,(H,14,15)(H2,11,12,13)/b10-7+ Key: GVVPGTZRZFNKDS-JXMROGBWBE;
	SMILES O=P(O)(O)OP(=O)(OC/C=C(/CC\C=C(/C)C)C)O;
Properties
Chemical formula	C10H17O7P2
Molar mass	311.19
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Geranyl pyrophosphate (GPP), also known as geranyl diphosphate (GDP), is the pyrophosphate ester of the terpenoid geraniol. Its salts are colorless. It is a precursor to many thousands of natural products.^[1]

^ Sell, Charles S. (2006). "Terpenoids". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.2005181602120504.a01.pub2. ISBN 0471238961.

[KO-1] Sell, Charles S. (2006). "Terpenoids". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.2005181602120504.a01.pub2. ISBN 0471238961.

[1]