Revision as of 14:20, 18 July 2011 editNono64 (talk | contribs)Autopatrolled, Pending changes reviewers, Rollbackers96,246 editsm Category:Phenolic compounds in wine← Previous edit | Latest revision as of 10:27, 25 November 2024 edit undoGraeme Bartlett (talk | contribs)Administrators250,307 edits chemspider | ||
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{{chembox | {{chembox | ||
| Watchedfields = changed | |||
| verifiedrevid = 442297034 | |||
| Name = Castavinol C3 | | Name = Castavinol C3 | ||
| ImageFile = Castavinol. |
| ImageFile = Castavinol 3.svg | ||
| ImageSize = 200px | | ImageSize = 200px | ||
| ImageName = Chemical structure of castavinol C3 | | ImageName = Chemical structure of castavinol C3 | ||
Line 7: | Line 9: | ||
| IUPACName = | | IUPACName = | ||
| OtherNames = <!-- <br> --> | | OtherNames = <!-- <br> --> | ||
|Section1= |
|Section1={{Chembox Identifiers | ||
| CASNo = | | CASNo = 183607-17-2 | ||
| CASNo_Ref = | | CASNo_Ref = {{cascite|correct|??}}= | ||
| ChemSpiderID = 59694876 | |||
| CASOther = | |||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
⚫ | | PubChem = | ||
| UNII = ZHZ5SCW9G9 | |||
⚫ | | PubChem = 57515151 | ||
| SMILES = OC2C(O)C(O)C(OC2CO)OC4C3C(C)(C(C)=O)OC4(c(cc1OC)cc(O)c1O)Oc5c3c(O)cc(O)c5 | | SMILES = OC2C(O)C(O)C(OC2CO)OC4C3C(C)(C(C)=O)OC4(c(cc1OC)cc(O)c1O)Oc5c3c(O)cc(O)c5 | ||
| SMILES1 = COc1cc(23Oc4cc(O)ccc4(2O2O(CO)(O)(O)2O)C(C)(C(C)=O)O3)cc(O)c1O | |||
| 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 | |||
| InChIKey = ADFRCNLBRJARNV-UHFFFAOYSA-N | |||
| InChIKey1 =ALSDFAORYWHNNX-UFFWUXHJSA-N | |||
| MeSHName = | | MeSHName = | ||
}} | }} | ||
|Section2= |
|Section2={{Chembox Properties | ||
| |
| C=26 | H=30 | O=14 | ||
| MolarMass = 566.50 g/mol | |||
| ExactMass = 566.163555 u | |||
| Appearance = | | Appearance = | ||
| Density = | | Density = | ||
| MeltingPt = |
| MeltingPt = | ||
| BoilingPt = |
| BoilingPt = | ||
| Solubility = | | Solubility = | ||
}} | }} | ||
| |
|Section3={{Chembox Hazards | ||
| MainHazards = | | MainHazards = | ||
| FlashPt = | | FlashPt = | ||
| |
| AutoignitionPt = | ||
| GHSPictograms = | |||
| RPhrases = <!-- {{R10}}, {{R23}}, {{R34}}, {{R50}} etc. --> | |||
| GHSSignalWord = | |||
| SPhrases = <!-- {{S1/2}}, {{S9}}, {{S16}}, {{S26}}, {{S36/37/39}}, {{S45}}, {{S61}} etc. --> | |||
| HPhrases = {{HPhrases|}} | |||
| PPhrases = {{PPhrases|}} | |||
| GHS_ref = <!-- no GHS data in pubchem Dec2021 --> | |||
}} | }} | ||
}} | }} | ||
⚫ | '''Castavinol C3''' is a ], a natural phenolic compound found in ].<ref>Castavinol, a new series of polyphenols from Bordeaux red wines |
||
⚫ | '''Castavinol C3''' is a ], a natural phenolic compound found in ]s.<ref>{{cite journal | doi = 10.1016/0040-4039(96)01761-3| title = Castavinol, a new series of polyphenols from Bordeaux red wines| date = 1996| last1 = Castagnino| first1 = Chantal| last2 = Vercauteren| first2 = Joseph| journal = Tetrahedron Letters| volume = 37| issue = 43| pages = 7739–7742}}</ref> | ||
⚫ | ==See also== | ||
⚫ | == See also == | ||
* ] | * ] | ||
==References== | == References == | ||
{{reflist}} | {{reflist}} | ||
==External links== | == External links == | ||
* (French) | * {{Webarchive|url=https://web.archive.org/web/20111004120343/http://www.socpharmbordeaux.asso.fr/pdf/pdf-136/136-019-036.pdf |date=2011-10-04 }} (French) | ||
] | ] | ||
] | |||
{{Natural-phenol-stub}} | |||
{{aromatic-stub}} |
Latest revision as of 10:27, 25 November 2024
Identifiers | |
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CAS Number | |
3D model (JSmol) | |
ChemSpider | |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
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SMILES
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Properties | |
Chemical formula | C26H30O14 |
Molar mass | 566.512 g·mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Castavinol C3 is a castavinol, a natural phenolic compound found in red wines.
See also
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 Misplaced Pages by expanding it. |