Compound Identification
SMILES
[Cl-].[Cl-].[Cl-].[Mn+3].ClC1=CC=CC(Cl)=C1C1=C2NC(C=C2)=C(C2=NC(C=C2)=C(C2=NC(C=C2)=C(C2=CC=C1N2)C1=C(Cl)C=CC=C1Cl)C1=C(Cl)C=CC=C1Cl)C1=C(Cl)C=CC=C1Cl
InChIKey
InChIKey=OHPVPEGFRCTMGP-UHFFFAOYSA-K
Formula
C44H22Cl11MnN4
Mass
1051.58
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Tetrapyrroles and derivatives
- Subclass Porphyrins
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Class
Tetrapyrroles and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Tetrapyrroles and derivatives
Subclass
Porphyrins
Intermediate Tree Nodes
Not available
Direct Parent
Porphyrins
Alternative Parents
Dichlorobenzenes Aryl chlorides Pyrroles Heteroaromatic compounds Organic transition metal salts Organic metal halides Azacyclic compounds Organonitrogen compounds Organochlorides Organic zwitterions Organic chloride salts Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Porphyrin - 1,3-dichlorobenzene - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Pyrrole - Organic transition metal salt - Azacycle - Organic metal halide - Organic nitrogen compound - Organic chloride salt - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrocarbon derivative - Organic zwitterion - Organic salt - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as porphyrins. These are compounds containing a fundamental skeleton of four pyrrole nuclei united through the alpha-positions by four methine groups to form a macrocyclic structure.
External Descriptors
Not available