[Cl-].[Cl-].[Cl-].[Cl-].[Cu++].CN(C)C(SCC1=CC2=C(C=C1)C1=NC3=NC(=NC4=C5C=C(CSC(N(C)C)=[N+](C)C)C=CC5=C([N-]4)N=C4N=C(N=C2[N-]1)C1=C4C=C(CSC(N(C)C)=[N+](C)C)C=C1)C1=C3C=CC(CSC(N(C)C)=[N+](C)C)=C1)=[N+](C)C

InChIKey=KDXHLJMVLXJXCW-UHFFFAOYSA-J

C56H68Cl4CuN16S4

1298.86

Organic compounds

Organoheterocyclic compounds

Tetrapyrroles and derivatives

Phthalocyanines

Not available

Phthalocyanines

Isoindoles Benzenoids Pyrroles Heteroaromatic compounds Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Organic metal halides Carboximidamides Azacyclic compounds Organic copper salts Organic chloride salts Hydrocarbon derivatives Organic cations

Aromatic heteropolycyclic compounds

Phthalocyanine skeleton - Isoindole - Isoindole or derivatives - Benzenoid - Pyrrole - Heteroaromatic compound - Organic metal halide - Carboximidamide - Sulfenyl compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic transition metal salt - Organonitrogen compound - Organosulfur compound - Hydrocarbon derivative - Organic salt - Organic chloride salt - Organic nitrogen compound - Organic copper salt - Organic cation - Aromatic heteropolycyclic compound

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.

Not available