Elenolic acid

Elenolic acid

Names
IUPAC name 2-[(2S,3S,4S)-3-formyl-5-methoxycarbonyl-2-methyl-3, 4-dihydro-2H-pyran-4-yl]acetic acid
Identifiers
CAS Number	34422-12-3 Y
3D model (Jmol)	Interactive image Interactive image
ChemSpider	148325 Y
PubChem	169607
InChI InChI=1S/C11H14O6/c1-6-8(4-12)7(3-10(13)14)9(5-17-6)11(15)16-2/h4-8H,3H2,1-2H3,(H,13,14)/t6-,7-,8+/m0/s1 Y Key: MQFAJBBHEYTHKF-BIIVOSGPSA-N Y InChI=1/C11H14O6/c1-6-8(4-12)7(3-10(13)14)9(5-17-6)11(15)16-2/h4-8H,3H2,1-2H3,(H,13,14)/t6-,7-,8+/m0/s1 Key: MQFAJBBHEYTHKF-BIIVOSGPBN
SMILES CC1C(C(C(=CO1)C(=O)OC)CC(=O)O)C=O O=C[C@H]1[C@@H](C(=C\O[C@H]1C)/C(=O)OC)CC(=O)O
Properties
Chemical formula	C11H14O6
Molar mass	242.23 g·mol−1
Density	1.308 g/mL
Boiling point	408.9 °C (768.0 °F; 682.0 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Elenolic acid is a component of olive oil and olive leaf extract. It can be considered as a marker for maturation of olives.^[1]

Oleuropein, a chemical compound found in olive leaf from the olive tree, together with other closely related compounds such as 10-hydroxyoleuropein, ligstroside and 10-hydroxyligstroside, are tyrosol esters of elenolic acid.

References

1. ↑ Esti, M; Cinquanta, L; La Notte, E (1998). "Phenolic Compounds in Different Olive Varieties". Journal of Agricultural and Food Chemistry. 46 (1): 32–35. doi:10.1021/jf970391. PMID 10554192.