CN(C)CC1=CC=CC=C1O[C@@H]1O[C@@H]2COC(C)(C)O[C@H]2[C@H](OP(C2=CC(C)=CC(C)=C2)C2=CC(C)=CC(C)=C2)[C@H]1OP(C1=CC(C)=CC(C)=C1)C1=CC(C)=CC(C)=C1

InChIKey=WEADTUXOJGYSKO-OOWGBTMCSA-N

C50H61NO6P2

833.987

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Pyranodioxins m-Xylenes Benzylamines Phenylmethylamines Phenoxy compounds Phenol ethers Aralkylamines Ketals Monosaccharides 1,3-dioxanes Oxanes Trialkylamines Oxacyclic compounds Organopnictogen compounds Organophosphorus compounds Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Phenolic glycoside - Pyranodioxin - Phenoxy compound - M-xylene - Xylene - Benzylamine - Phenol ether - Phenylmethylamine - Ketal - Aralkylamine - Meta-dioxane - Monocyclic benzene moiety - Monosaccharide - Oxane - Benzenoid - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Oxacycle - Acetal - Organophosphorus compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Organic nitrogen compound - Aromatic heteropolycyclic 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