CC(=O)N(C(=O)CC(=O)N1N=C(C(N=NC2=CC=CC=C2[NH+](O)[O-])C1=O)C1=CC=CC=C1)C1=CC=C(Cl)C=C1

InChIKey=MVWUHSJNUKIRMM-UHFFFAOYSA-N

C26H21ClN6O6

548.94

Organic compounds

Benzenoids

Benzene and substituted derivatives

Anilides

Acetanilides - Haloacetanilides

P-haloacetanilides

Alpha amino acids and derivatives Chlorobenzenes Pyrazolones 1,3-dicarbonyl compounds Aryl chlorides N-substituted carboxylic acid imides Acetamides Dicarboximides Azo compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds N-organohydroxylamines Organic salts Organopnictogen compounds Organic zwitterions Organic oxides Organochlorides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

P-haloacetanilide - Alpha-amino acid or derivatives - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Carboxylic acid imide, n-substituted - Pyrazolinone - 1,3-dicarbonyl compound - Carboxylic acid imide - Dicarboximide - Pyrazoline - Acetamide - Azo compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - N-organohydroxylamine - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Azacycle - Organic zwitterion - Organohalogen compound - Organochloride - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Organic salt - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as p-haloacetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group, which is in turn para-substituted with a halogen atom.

Not available