CC1CCC2=C(C1)C=C(C#N)C(SCC(=O)NC1=C(Br)C=C(C=C1Br)[N+]([O-])=O)=N2

InChIKey=OWGINZYHYIQYPK-UHFFFAOYSA-N

C19H16Br2N4O3S

540.23

Organic compounds

Organoheterocyclic compounds

Quinolines and derivatives

Hydroquinolines

Not available

Hydroquinolines

Anilides Nitrobenzenes Nitroaromatic compounds N-arylamides Alkylarylthioethers Bromobenzenes Pyridines and derivatives Aryl bromides Heteroaromatic compounds Secondary carboxylic acid amides Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Nitriles Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Organobromides

Aromatic heteropolycyclic compounds

Tetrahydroquinoline - Nitrobenzene - Anilide - N-arylamide - Aryl thioether - Nitroaromatic compound - Alkylarylthioether - Bromobenzene - Halobenzene - Monocyclic benzene moiety - Aryl bromide - Aryl halide - Pyridine - Benzenoid - Heteroaromatic compound - Organic nitro compound - Secondary carboxylic acid amide - C-nitro compound - Carboxamide group - Carboxylic acid derivative - Azacycle - Carbonitrile - Nitrile - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Thioether - Sulfenyl compound - Carbonyl group - Organic oxide - Cyanide - Organic oxygen compound - Organohalogen compound - Hydrocarbon derivative - Organobromide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic zwitterion - Organic nitrogen compound - Organic salt - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.

Not available