Compound Identification
SMILES
Cl[Ru++]Cl.NC(C(N)C1=CC=CC=C1)C1=CC=CC=C1.C#CC#CC#C[PH+](C#CC#CC#C)C1=C(SC2=C(C=CC3=CC=CC=C23)[PH+](C#CC#CC#C)C#CC#CC#C)C2=CC=CC=C2C=C1
InChIKey
InChIKey=GADWVCAWLAMEOH-UHFFFAOYSA-N
Formula
C58H34Cl2N2P2RuS
Mass
1024.9
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
Diarylthioethers Naphthalenes Thiophenol ethers Aralkylamines Benzene and substituted derivatives Sulfenyl compounds Organic transition metal salts Organic metal halides Acetylides Organophosphorus compounds Monoalkylamines Hydrocarbon derivatives Organic cations
Molecular Framework
Not available
Substituents
Stilbene - Diarylthioether - Naphthalene - Aryl thioether - Thiophenol ether - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Organic metal halide - Acetylide - Thioether - Sulfenyl compound - Organic metal salt - Organic transition metal salt - Primary amine - Organosulfur compound - Organophosphorus compound - Organic nitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Amine - Organonitrogen compound - Organic cation - Aromatic homopolycyclic 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