Identification | Back Directory | [Name]
3-p-Coumaroylquinic acid | [CAS]
1899-30-5 | [Synonyms]
5-p-coumaroylquinicaci 3-p-Coumaroylquinic acid 3-O-p-Coumaroyl quinic acid 1β,3β,4β-Trihydroxy-5α-[[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]oxy]cyclohexanecarboxylic acid (1S)-1β,3β,4β-Trihydroxy-5α-[[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]oxy]-1α-cyclohexanecarboxylic acid Cyclohexanecarboxylic acid, 1,3,4-trihydroxy-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, (1S,3R,4R,5R)- | [Molecular Formula]
C16H18O8 | [MOL File]
1899-30-5.mol | [Molecular Weight]
338.31 |
Chemical Properties | Back Directory | [Melting point ]
247-248 °C(Solv: water (7732-18-5)) | [Boiling point ]
613.2±55.0 °C(Predicted) | [density ]
1.55±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [form ]
solid | [pka]
3.91±0.50(Predicted) | [color ]
white to light yellow |
Hazard Information | Back Directory | [Uses]
A naturally occurring substance discovered in plants, which possesses antibacterial characteristics and may serve as a substitute for antibiotics in combatting opportunistic fungal infections. | [Definition]
ChEBI: 5-p-coumaroylquinic acid is a cinnamate ester obtained by formal condensation of the carboxy group of 4-coumaric acid with the 5-hydroxy group of (-)-quinic acid. It has a role as a metabolite. It is a cinnamate ester and a cyclitol carboxylic acid. It is functionally related to a (-)-quinic acid and a 4-coumaric acid. |
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Merck KGaA
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