Cl.COC1=CC(OCC(C)C)=C(C=C1)C1=NC(C(N1C(=O)N1CCNCC1)C1=CC=C(Cl)C=C1)C1=CC=C(Cl)C=C1

InChIKey=JWKPQFRUXCPVPK-UHFFFAOYSA-N

C31H35Cl3N4O3

618.0

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Not available

Not available

Stilbenes

Piperazine carboxamides Phenoxy compounds Anisoles Methoxybenzenes Alkyl aryl ethers Chlorobenzenes Aryl chlorides Imidazolines Ureas Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Dialkylamines Carboximidamides Carboxamidines Carbonyl compounds Hydrocarbon derivatives Hydrochlorides Organic oxides Organochlorides

Aromatic heteromonocyclic compounds

Stilbene - Piperazine-1-carboxamide - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Chlorobenzene - Halobenzene - Piperazine - Aryl chloride - 1,4-diazinane - Benzenoid - Monocyclic benzene moiety - Aryl halide - 2-imidazoline - Urea - Amidine - Azacycle - Carboxylic acid amidine - Secondary aliphatic amine - Organoheterocyclic compound - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Secondary amine - Organic oxygen compound - Hydrochloride - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Amine - 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