C[S@](=O)C[C@H]1O[C@@H](OC2=CC=C(C=C2)[N+]([O-])=O)[C@H](O)[C@@H](O)[C@H]1O

InChIKey=MOOOBRASVALCAF-UTJNMCDLSA-N

C13H17NO8S

347.34

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Nitrobenzenes Nitroaromatic compounds Phenol ethers Phenoxy compounds Monosaccharides Oxanes Sulfoxides Secondary alcohols Oxacyclic compounds Organic oxoazanium compounds Sulfinyl compounds Acetals Polyols Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic salts Organic oxides

Aromatic heteromonocyclic compounds

Phenolic glycoside - O-glycosyl compound - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - C-nitro compound - Organic nitro compound - Secondary alcohol - Sulfoxide - Acetal - Oxacycle - Organic oxoazanium - Organoheterocyclic compound - Polyol - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfinyl compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organosulfur compound - Organic nitrogen compound - Organic salt - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organic zwitterion - 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