CC1=CC(NC(=O)CSC2=NC(C)=C(C(=O)NC3=CC=CC=C3C)C(C3=CC=CC=C3Cl)=C2C#N)=CC(C)=C1

InChIKey=MOCMVLSQBBDDBD-UHFFFAOYSA-N

C31H27ClN4O2S

555.09

Organic compounds

Benzenoids

Benzene and substituted derivatives

Anilides

Not available

Aromatic anilides

Phenylpyridines Nicotinamides m-Xylenes 3-pyridinecarbonitriles N-arylamides Toluenes Alkylarylthioethers Methylpyridines Chlorobenzenes Aryl chlorides Heteroaromatic compounds Secondary carboxylic acid amides Sulfenyl compounds Nitriles Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteromonocyclic compounds

Aromatic anilide - 4-phenylpyridine - Pyridine carboxylic acid or derivatives - Pyridinecarboxamide - Nicotinamide - Aryl thioether - N-arylamide - M-xylene - Xylene - 3-pyridinecarbonitrile - Toluene - Alkylarylthioether - Chlorobenzene - Methylpyridine - Halobenzene - Aryl chloride - Pyridine - Aryl halide - Heteroaromatic compound - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Carbonitrile - Nitrile - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organohalogen compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Cyanide - Organic oxide - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group.

Not available