CC1=CC=CC=C1CC(C(=O)NN=CC1=CC=C(O1)C1=C(Br)C=C(C=C1)[N+]([O-])=O)C1=CC=CC=C1

InChIKey=RAVVKLOEGHGNKB-UHFFFAOYSA-N

C27H22BrN3O4

532.394

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Not available

Not available

Stilbenes

Phenylacetamides Nitrobenzenes Nitroaromatic compounds Toluenes Bromobenzenes Aryl bromides Furans Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Carboxylic acids and derivatives Organic oxoazanium compounds Organobromides Hydrocarbon derivatives Organonitrogen compounds Organopnictogen compounds Organic zwitterions Organic oxides Carbonyl compounds Organic salts

Aromatic heteromonocyclic compounds

Stilbene - Phenylacetamide - Nitrobenzene - Nitroaromatic compound - Bromobenzene - Halobenzene - Toluene - Monocyclic benzene moiety - Aryl bromide - Aryl halide - Benzenoid - Heteroaromatic compound - Furan - Organic nitro compound - C-nitro compound - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Carbonyl group - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic salt - Organobromide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Organopnictogen compound - Organic zwitterion - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Not available