OP(O)(O)=O.CCN(CC)CCCC(C)NC1=CC(=NC2=C1C=CC(Cl)=C2)C(=C)C1=CC=C(O1)[N+]([O-])=O

InChIKey=PLJNWBDLPZOZBS-UHFFFAOYSA-N

C24H32ClN4O7P

554.96

Organic compounds

Organoheterocyclic compounds

Quinolines and derivatives

Aminoquinolines and derivatives

Not available

4-aminoquinolines

Chloroquinolines Nitrofurans Nitroaromatic compounds Secondary alkylarylamines Aminopyridines and derivatives Aryl chlorides Organic phosphoric acids and derivatives Benzenoids Heteroaromatic compounds Trialkylamines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Organic oxoazanium compounds Organooxygen compounds Hydrocarbon derivatives Organic oxides Organic salts Organochlorides Organic cations

Aromatic heteropolycyclic compounds

4-aminoquinoline - Haloquinoline - Chloroquinoline - Nitroaromatic compound - 2-nitrofuran - Aminopyridine - Secondary aliphatic/aromatic amine - Benzenoid - Aryl chloride - Pyridine - Organic phosphoric acid derivative - Aryl halide - Furan - Heteroaromatic compound - Tertiary aliphatic amine - Tertiary amine - Organic nitro compound - C-nitro compound - Oxacycle - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Secondary amine - Allyl-type 1,3-dipolar organic compound - Organochloride - Organic salt - Organohalogen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Amine - Organic cation - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 4-aminoquinolines. These are organic compounds containing an amino group attached to the 4-position of a quinoline ring system.

Not available