COC1=CC=C(C=C1)S(=O)(=O)C(=CC1=CC=CC=C1[N+]([O-])=O)C(=O)C1=CC=CC=C1

InChIKey=IVHDTQLYTHMMQY-UHFFFAOYSA-N

C22H17NO6S

423.44

Organic compounds

Phenylpropanoids and polyketides

Linear 1,3-diarylpropanoids

Chalcones and dihydrochalcones

Not available

Retrochalcones

Cinnamic acids and derivatives Benzenesulfonyl compounds Nitrobenzenes Anisoles Aryl ketones Benzoyl derivatives Methoxybenzenes Nitroaromatic compounds Phenoxy compounds Alkyl aryl ethers Alpha-branched alpha,beta-unsaturated ketones Acryloyl compounds Enones Sulfones Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organic oxides Organic salts Organonitrogen compounds Organic cations

Aromatic homomonocyclic compounds

Retrochalcone - Cinnamic acid or derivatives - Nitrobenzene - Benzenesulfonyl group - Anisole - Benzoyl - Methoxybenzene - Phenoxy compound - Aryl ketone - Phenol ether - Nitroaromatic compound - Alkyl aryl ether - Monocyclic benzene moiety - Alpha-branched alpha,beta-unsaturated-ketone - Benzenoid - Acryloyl-group - Alpha,beta-unsaturated ketone - Enone - Sulfonyl - Sulfone - Organic nitro compound - Ketone - C-nitro compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Ether - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Organosulfur compound - Organic cation - Aromatic homomonocyclic compound

This compound belongs to the class of organic compounds known as retrochalcones. These are a form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.

Not available