OC1C(CNS(=O)(=O)C2=CC=CC(=C2)C(F)(F)F)OC(OC2=CC=C(I)C=C2)C(O)C1OCC=C

InChIKey=FTNMJJFHRBTWTA-UHFFFAOYSA-N

C22H23F3INO7S

629.39

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

O-glycosyl compounds Trifluoromethylbenzenes Benzenesulfonamides Benzenesulfonyl compounds Phenoxy compounds Phenol ethers Iodobenzenes Aryl iodides Oxanes Monosaccharides Organosulfonamides Aminosulfonyl compounds Secondary alcohols Acetals Oxacyclic compounds Dialkyl ethers Organic oxides Hydrocarbon derivatives Alkyl fluorides Organofluorides Organoiodides Organonitrogen compounds Organopnictogen compounds

Aromatic heteromonocyclic compounds

Phenolic glycoside - O-glycosyl compound - Trifluoromethylbenzene - Benzenesulfonamide - Benzenesulfonyl group - Phenoxy compound - Phenol ether - Iodobenzene - Halobenzene - Aryl halide - Monosaccharide - Oxane - Aryl iodide - Organosulfonic acid amide - Monocyclic benzene moiety - Benzenoid - Sulfonyl - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Secondary alcohol - Acetal - Dialkyl ether - Ether - Oxacycle - Organoheterocyclic compound - Alkyl halide - Alkyl fluoride - Alcohol - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organosulfur compound - Organonitrogen compound - Organohalogen compound - Organofluoride - Organoiodide - 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