Syringin | |
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4-[(1E)-3-Hydroxyprop-1-en-1-yl]-2,6-dimethoxyphenyl β-D-glucopyranoside |
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Other names
Eleutheroside B; Ilexanthin A; Ligustrin; Lilacin; Magnolenin; Methoxyconiferine; Sinapyl alcohol 4-O-glucoside; Siringin; Syringoside |
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Identifiers | |
CAS number | 118-34-3 |
PubChem | 5316860 |
ChemSpider | 4475831 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C17H24O9 |
Molar mass | 372.37 g mol−1 |
Appearance | White crystalline solid |
Melting point |
192 °C, 465 K, 378 °F ([1]) |
Solubility in water | Slightly soluble[1] |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Infobox references |
Syringin is a natural chemical compound first isolated from the bark of lilac (Syringa vulgaris) by Meillet in 1841.[1] It has since been found to be distributed widely throughout many types of plants. Chemically, it is the glucoside of sinapyl alcohol.