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

InChIKey=PNLOGKKMDRZCQE-UUWLPUTASA-N

C13H14N2O8

326.261

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses O-glycosyl compounds Nitrobenzenes Benzonitriles Nitroaromatic compounds Phenol ethers Phenoxy compounds Oxanes Secondary alcohols Oxacyclic compounds Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Acetals Nitriles Polyols Organopnictogen compounds Organic zwitterions Organic salts Organic oxides Primary alcohols Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - O-glycosyl compound - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Benzonitrile - Phenol ether - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - 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 - Carbonitrile - Polyol - Organoheterocyclic compound - Nitrile - Acetal - Organic oxoazanium - Oxacycle - Organic salt - Hydrocarbon derivative - Organonitrogen compound - Alcohol - Primary alcohol - Organic oxide - Cyanide - Organopnictogen compound - Organic nitrogen compound - 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