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

InChIKey=JPZSNDRVIVSQHG-UHFFFAOYSA-N

C18H16N2O5

340.335

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids Nitrobenzenes Nitroaromatic compounds Ketones Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organonitrogen compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations

Aromatic homomonocyclic compounds

Norlignan skeleton - Linear 1,3-diarylpropanoid - Nitrobenzene - Nitroaromatic compound - Monocyclic benzene moiety - Benzenoid - Ketone - C-nitro compound - Organic nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organonitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic cation - Aromatic homomonocyclic compound

This compound belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

Not available