Structure Information
Structure

Compound Identification

SMILES

[Zn++].CCCCOC1=C(OCCCC)C=C2C3=NC4=NC(=NC5=C6C=C(C#CC7=CC=C(C=C7)[N+]([O-])=O)C(=CC6=C([N-]5)N=C5N=C(N=C([N-]3)C2=C1)C1=CC(OCCCC)=C(OCCCC)C=C51)C#CC1=CC=C(C=C1)[N+]([O-])=O)C1=CC(OCCCC)=C(OCCCC)C=C41

InChIKey

InChIKey=WCWBZQMQRBLQBC-UHFFFAOYSA-N

Formula

C72H70N10O10Zn

Mass

1300.79

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Tetrapyrroles and derivatives

Subclass

Phthalocyanines

Intermediate Tree Nodes

Not available

Direct Parent

Phthalocyanines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phthalocyanine skeleton - Isoindole - Isoindole or derivatives - Nitrobenzene - Nitroaromatic compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Pyrrole - Heteroaromatic compound - Organic nitro compound - C-nitro compound - Organic transition metal salt - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Ether - Organic oxoazanium - Organic salt - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Organic zwitterion - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phthalocyanines. These are cyclic tetrapyrroles that contain a phthalocyanine skeleton, which consists of four isoindole-type units, with the connecting carbon atoms in the macrocycle replaced by nitrogen.

External Descriptors

Not available

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