// Workers AI · dad joke modeWhat did Castavinol C3 say to its date? "You've got a binding attraction

Castavinol C3

Chemical structure of castavinol C3
Identifiers
CAS Number	183607-17-2 Y=
3D model (JSmol)	Interactive image Interactive image
ChemSpider	59694876
PubChem CID	57515151
UNII	ZHZ5SCW9G9 Y
CompTox Dashboard (EPA)	DTXSID301029755
InChI InChI=1S/C26H30O14/c1-9(28)25(2)18-17-12(30)6-11(29)7-14(17)39-26(40-25,10-4-13(31)19(32)15(5-10)36-3)23(18)38-24-22(35)21(34)20(33)16(8-27)37-24/h4-7,16,18,20-24,27,29-35H,8H2,1-3H3 Key: ADFRCNLBRJARNV-UHFFFAOYSA-N Key: ALSDFAORYWHNNX-UFFWUXHJSA-N
SMILES OC2C(O)C(O)C(OC2CO)OC4C3C(C)(C(C)=O)OC4(c(cc1OC)cc(O)c1O)Oc5c3c(O)cc(O)c5 COc1cc([C@@]23Oc4cc(O)ccc4[C@@H]([C@H]2O[C@@H]2O[C@@H](CO)[C@@H](O)[C@H](O)[C@@H]2O)C(C)(C(C)=O)O3)cc(O)c1O
Properties
Chemical formula	C26H30O14
Molar mass	566.512 g·mol−1
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

Castavinol C3 is a castavinol, a natural phenolic compound found in red wines.

See also

• phenolic compounds found in wine

External links

• 1996 : Les molécules des futurs millésimes Bordelais ? C. Castagnino, C. Chèze and J. Vercauteren, Bull. Soc. Pharm. Bordeaux, 1997, 136, pp. 19-36 Archived 2011-10-04 at the Wayback Machine (French)