Compound Identification
SMILES
CC1=CC=C(C=C1)S(=O)(=O)OCC1(COS(=O)(=O)C2=CC=C(C)C=C2)CC(=C(C1)C1=CC2=C(OCO2)C=C1)C1=CC=C(C=C1)S(C)(=O)=O
InChIKey
InChIKey=AYNCTHOFFSGPEP-UHFFFAOYSA-N
Formula
C35H34O10S3
Mass
710.83
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Stilbenes
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Stilbenes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Stilbenes
Alternative Parents
p-Methylbenzenesulfonates Benzenesulfonate esters Tosyl compounds Benzodioxoles Benzenesulfonyl compounds Arylsulfonic acids and derivatives Organosulfonic acid esters Sulfones Oxacyclic compounds Acetals Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Stilbene - Benzenesulfonate ester - P-methylbenzenesulfonate - Tosyl compound - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Benzodioxole - Toluene - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid ester - Sulfone - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Acetal - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
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.
External Descriptors
Not available