ENSIKLOPEDIA Cari Tekan Enter untuk memulai pencarian cepat. Kembali ke Ensiklopedia Arsip Wikipedia Indonesia Castavinol C3 Castavinol C3 Castavinol C3 Chemical structure of castavinol C3 Identifiers CAS Number 183607-17-2 Y= 3D model (JSmol) Interactive imageInteractive 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,8H2,1-3H3Key: ADFRCNLBRJARNV-UHFFFAOYSA-NKey: 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)c5COc1cc([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 Chemical compound Castavinol C3 is a castavinol, a natural phenolic compound found in red wines.[1] See also phenolic compounds found in wine References ↑ Castagnino, Chantal; Vercauteren, Joseph (1996). "Castavinol, a new series of polyphenols from Bordeaux red wines". Tetrahedron Letters. 37 (43): 7739–7742. doi:10.1016/0040-4039(96)01761-3. 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) This article about an aromatic compound is a stub. You can help Wikipedia by adding missing information.vte
