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

InChIKey=RMQNVZDXEMOJCW-MTAIEDJOSA-N

C12H15NO8

301.251

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Pentoses Nitrobenzenes Nitroaromatic compounds Phenoxy compounds Phenol ethers Oxolanes Secondary alcohols Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Acetals Oxacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic salts Organic oxides Primary alcohols Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

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