Compound Identification
SMILES
[Ni++].[O-][N+](=O)C1=CC=C(OC2=C3C=CC(=N3)C(=C3[N-]C(C=C3)=C(Br)C3=CC=C([N-]3)C(=C3C=CC2=N3)C2=CC=CC=C2)C2=CC=CC=C2)C=C1
InChIKey
InChIKey=RPFYRFIOPZOQMU-UHFFFAOYSA-N
Formula
C38H22BrN5NiO3
Mass
735.223
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
Diarylethers Nitrobenzenes Phenoxy compounds Phenol ethers Nitroaromatic compounds Aryl bromides Pyrroles Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic transition metal salts Organic oxoazanium compounds Organic metal halides Hydrocarbon derivatives Organic oxides Organic zwitterions Organobromides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Porphyrin - Diaryl ether - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Pyrrole - Organic nitro compound - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Ether - Organic metal halide - Organic transition metal salt - Organic oxoazanium - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Organobromide - Organonitrogen compound - Organohalogen compound - Organooxygen compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - 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