OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@H]1O)C1=CC=CC=C1N=C=S

InChIKey=GGYBJYNRLGNUNZ-SJHCENCUSA-N

C13H15NO5S

297.33

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

C-glycosyl compounds Oxanes Monosaccharides Benzene and substituted derivatives Secondary alcohols Isothiocyanates Propargyl-type 1,3-dipolar organic compounds Polyols Oxacyclic compounds Dialkyl ethers Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - C-glycosyl compound - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Isothiocyanate - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Polyol - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organonitrogen compound - Organosulfur compound - Organopnictogen compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Not available