CC1=C(C(C)=NO1)S(=O)(=O)N(CC#C)C(=O)C1=CC=C(O1)C1=C(C=C(Cl)C=C1)[N+]([O-])=O

InChIKey=KLNFHHYCCYHATA-UHFFFAOYSA-N

C19H14ClN3O7S

463.85

Organic compounds

Benzenoids

Benzene and substituted derivatives

Nitrobenzenes

Not available

Nitrobenzenes

Furoic acid and derivatives Nitroaromatic compounds Chlorobenzenes Aryl chlorides Organosulfonic acids and derivatives Aminosulfonyl compounds Heteroaromatic compounds Isoxazoles Azacyclic compounds Carboxylic acids and derivatives Acetylides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Oxacyclic compounds Organopnictogen compounds Organochlorides Hydrocarbon derivatives Organooxygen compounds Organonitrogen compounds Organic oxides

Aromatic heteromonocyclic compounds

Nitrobenzene - Furoic acid or derivatives - Nitroaromatic compound - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Azole - Furan - Heteroaromatic compound - Isoxazole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - C-nitro compound - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Acetylide - Oxacycle - Azacycle - Organic oxoazanium - Organoheterocyclic compound - Organic 1,3-dipolar compound - Organopnictogen compound - Organohalogen compound - Organic oxide - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.

Not available