CCOC(=O)C1=CC(COC2=CC=C(C=C2)C2=NN(CC2(O)C2=CC=CC=C2)C(\N)=N\S(=O)(=O)C2=CC=C(Cl)C=C2)=CC=C1

InChIKey=SAUQADBVUDOUED-UHFFFAOYSA-N

C32H29ClN4O6S

633.12

Organic compounds

Phenylpropanoids and polyketides

Stilbenes

Not available

Not available

Stilbenes

Benzenesulfonamides Benzoic acid esters Benzenesulfonyl compounds Phenoxy compounds Phenol ethers Benzoyl derivatives Alkyl aryl ethers Chlorobenzenes Aryl chlorides Tertiary alcohols Sulfonyls Pyrazolines Organosulfonic acids and derivatives Carboxylic acid esters Guanidines Azacyclic compounds Organochlorides Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Stilbene - Benzenesulfonamide - Benzoate ester - Benzenesulfonyl group - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Tertiary alcohol - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Pyrazoline - Guanidine - Carboxylic acid ester - Azacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Organic oxide - Organic nitrogen compound - Alcohol - Organic oxygen compound - Organohalogen compound - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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