Coutaric acid
Names | |
---|---|
Preferred IUPAC name (2R,3R)-2-Hydroxy-3-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}butanedioic acid | |
Other names trans-coutaric acid cis-coutaric acid trans-p-Coumaroyltartaric acid cis-p-coumaroyl-(+)-tartaric acid trans-p-coumaroyl-(+)-tartaric acid cis-Coumaroyl tartaric acidbr>trans-Coumaroyl tartaric acid | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChEBI |
|
ChemSpider |
|
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C13H12O8 |
Molar mass | 296.231 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Coutaric acid is a hydroxycinnamoyltartaric acid found in wine, pomace[1] and grape.[2] It is an ester formed from coumaric acid and tartaric acid.
References
- ^ Maier, T.; Sanzenbacher, S.; Kammerer, D. R.; Berardini, N.; Conrad, J. R.; Beifuss, U.; Carle, R.; Schieber, A. (2006). "Isolation of hydroxycinnamoyltartaric acids from grape pomace by high-speed counter-current chromatography". Journal of Chromatography A. 1128 (1–2): 61–67. doi:10.1016/j.chroma.2006.06.082. PMID 16860334.
- ^ Singleton, V. L.; Zaya, J.; Trousdale, E. K. (1986). "Caftaric and coutaric acids in fruit of Vitis". Phytochemistry. 25 (9): 2127. doi:10.1016/0031-9422(86)80078-4.
- v
- t
- e
Types of hydroxycinnamic acids
Precursor | |
---|---|
Monohydroxycinnamic acids (Coumaric acids) |
|
Dihydroxycinnamic acids |
|
Trihydroxycinnamic acids |
|
O-methylated forms | |
others |
glycoside-likes |
| ||||||||
---|---|---|---|---|---|---|---|---|---|
Tartaric acid esters |
| ||||||||
Other esters with caffeic acid |
| ||||||||
Caffeoyl phenylethanoid glycoside (CPG) |
|
Dimers |
|
---|---|
Trimers |
|
Tetramers |
|
coenzyme A (CoA)
- Caffeoyl-CoA
- Cinnamoyl-CoA
- Coumaroyl-CoA
This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
- v
- t
- e