OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)C1=CC(CC2=NC=C(S2)C2=CC=CO2)=C(Cl)C=C1F

InChIKey=HAEKNRTVYKAKQV-QSWMPLQWSA-N

C20H19ClFNO6S

455.88

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Phenolic glycosides

Hexoses C-glycosyl compounds 2,5-disubstituted thiazoles Chlorobenzenes Fluorobenzenes Aryl fluorides Aryl chlorides Oxanes Heteroaromatic compounds Furans Secondary alcohols Dialkyl ethers Azacyclic compounds Oxacyclic compounds Polyols Organonitrogen compounds Organofluorides Organochlorides Hydrocarbon derivatives Primary alcohols

Aromatic heteromonocyclic compounds

Phenolic glycoside - Hexose monosaccharide - C-glycosyl compound - 2,5-disubstituted 1,3-thiazole - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Oxane - Monosaccharide - Heteroaromatic compound - Azole - Thiazole - Furan - Secondary alcohol - Polyol - Ether - Dialkyl ether - Organoheterocyclic compound - Azacycle - Oxacycle - Primary alcohol - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organohalogen compound - Organochloride - Organofluoride - 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