OC[C@H]1O[C@@H](OC[C@H]2O[C@H](C[C@H]2O)N2C=C([80Br])C(=O)CC2=O)[C@H](O)[C@@H](O)[C@H]1O

InChIKey=YCXXQYRKZGWMDQ-INPOINNJSA-N

C16H22BrNO10

468.268

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

O-glycosyl compounds

Tetrahydropyridines Monosaccharides 1,3-dicarbonyl compounds Oxanes Vinylogous amides Tertiary carboxylic acid amides Alpha-haloketones Oxolanes Cyclic ketones Lactams Secondary alcohols Vinyl bromides Azacyclic compounds Bromoalkenes Acetals Oxacyclic compounds Polyols Hydrocarbon derivatives Organic oxides Organobromides Organonitrogen compounds Aldehydes Organopnictogen compounds Primary alcohols

Aliphatic heteromonocyclic compounds

O-glycosyl compound - Tetrahydropyridine - Hydropyridine - Monosaccharide - Oxane - 1,3-dicarbonyl compound - Alpha-haloketone - Oxolane - Vinylogous amide - Tertiary carboxylic acid amide - Carboxamide group - Ketone - Lactam - Secondary alcohol - Cyclic ketone - Acetal - Carboxylic acid derivative - Oxacycle - Azacycle - Bromoalkene - Haloalkene - Polyol - Organoheterocyclic compound - Vinyl halide - Vinyl bromide - Aldehyde - Organohalogen compound - Organobromide - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Alcohol - Primary alcohol - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Not available