Chemical constituents from Semiliquidambar chingii and their chemotaxonomic significance was written by Zhang, Jingyi;Kaliaperumal, Kumaravel;Liu, Ziyue;Zhang, Jun. And the article was included in Biochemical Systematics and Ecology in 2022.Safety of (2S,3R,4S,5S,6R)-2-(3-Hydroxy-5-((E)-4-hydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol The following contents are mentioned in the article:
The present study investigated the phytochem. constituents of Semiliquidambar chingii for the first time, resulting in the isolation and characterization of nineteen compounds which were categorized into eight groups as resveratrol derivatives (1-4), triterpenoids (5-10), flavonoids (11-13), phenolic glycosides (14-15), lignan (16), ellagic acid derivative (17), coniferyl alc. derivative (18), and shikimic acid derivative (19). The chem. structures of these compounds were elucidated based on the careful anal. of spectroscopic data and comparison with reported data. This is the first report of isolation of compounds 1-19 from S. chingii and compounds 1-4, 5-7, 9-11, and 14-19 within the genus Semiliquidambar. Furthermore, the chemotaxonomic significance of the isolates was discussed in detail, which might provide important chem. taxonomic evidence supporting the hybrid origin of Semiliquidambar from the genera Altingia and Liquidambar. This study involved multiple reactions and reactants, such as (2S,3R,4S,5S,6R)-2-(3-Hydroxy-5-((E)-4-hydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (cas: 27208-80-6Safety of (2S,3R,4S,5S,6R)-2-(3-Hydroxy-5-((E)-4-hydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol).
(2S,3R,4S,5S,6R)-2-(3-Hydroxy-5-((E)-4-hydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol (cas: 27208-80-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Safety of (2S,3R,4S,5S,6R)-2-(3-Hydroxy-5-((E)-4-hydroxystyryl)phenoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
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