CC1=C(C(=O)N(CC2=CC(Cl)=C(NC(=O)CBr)C(Cl)=C2)C(\N)=N\C(O)=O)C(=NO1)C1=CC=C(OCC=C)C=C1

InChIKey=JRFWAGVOCAOSQH-UHFFFAOYSA-N

C25H22BrCl2N5O6

639.28

Organic compounds

Benzenoids

Benzene and substituted derivatives

Anilides

Not available

Anilides

Phenoxy compounds Phenol ethers N-arylamides Dichlorobenzenes Alkyl aryl ethers Aryl chlorides Isoxazoles Heteroaromatic compounds Secondary carboxylic acid amides Guanidines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Carboximidamides Hydrocarbon derivatives Imines Carbonyl compounds Organic oxides Organobromides Alkyl bromides Organochlorides

Aromatic heteromonocyclic compounds

Anilide - Phenoxy compound - 1,3-dichlorobenzene - N-arylamide - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Azole - Heteroaromatic compound - Isoxazole - Carboxamide group - Guanidine - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic oxide - Organic oxygen compound - Alkyl halide - Alkyl bromide - Organic nitrogen compound - Hydrocarbon derivative - Imine - Carbonyl group - Organohalogen compound - Organobromide - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.

Not available