CC1=C2C=CN([C@@H]3OC[C@H](O)[C@H](O)[C@H]3O)C2=NC(Cl)=C1[N+]([O-])=O

InChIKey=LJTJYDKVGALRAE-UFAOYGAJSA-N

C13H14ClN3O6

343.72

Organic compounds

Organic oxygen compounds

Organooxygen compounds

Carbohydrates and carbohydrate conjugates

Glycosyl compounds

Glycosylamines

Pyrrolopyridines Nitroaromatic compounds 2-halopyridines Methylpyridines Substituted pyrroles Oxanes Aryl chlorides Heteroaromatic compounds Secondary alcohols 1,2-diols Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Organochlorides Organonitrogen compounds

Aromatic heteropolycyclic compounds

N-glycosyl compound - Pyrrolopyridine - Nitroaromatic compound - 2-halopyridine - Methylpyridine - Aryl chloride - Aryl halide - Oxane - Pyridine - Substituted pyrrole - Heteroaromatic compound - Pyrrole - 1,2-diol - C-nitro compound - Organic nitro compound - Secondary alcohol - Oxacycle - Azacycle - Organic oxoazanium - Organoheterocyclic compound - Polyol - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organochloride - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic nitrogen compound - Alcohol - Organohalogen compound - Organic zwitterion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether).

Not available