Structure Information
Structure

Compound Identification

SMILES

[Co++].[O-][Cl](=O)(=O)=O.CCCCCCCCCCCCCCCCCCOC(=O)C[C@@]1(C)[C@H](CCC(=O)OC)\C2=C\C3=N\C(\[C@@H](CCC(=O)OC)C3(C)C)=C(C)/C3=N[C@H]([C@H](CC(=O)OC)[C@@]3(C)CCC(=O)OC)[C@]3(C)N=C([C@@H](CCC(=O)OC)[C@]3(C)CC(=O)OC)\C(C)=C1/[N-]2

InChIKey

InChIKey=MEJQRTPZWUHIQH-WIWYBNISSA-M

Formula

C69H107ClCoN4O18

Mass

1375.01

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Tetrapyrroles and derivatives

Subclass

Corrinoids

Intermediate Tree Nodes

Not available

Direct Parent

Precorrins

Alternative Parents

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Precorrin - Metallotetrapyrrole skeleton - Fatty acid ester - Organic perchlorate - Fatty acyl - Organic perchlorate salt - Pyrrolidine - Pyrroline - Methyl ester - Carboxylic acid ester - Ketimine - Organic chlorate - Azacycle - Organic transition metal salt - Carboxylic acid derivative - Organic 1,3-dipolar compound - Carbene-type 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organic salt - Organic cobalt salt - Organic nitrogen compound - Imine - Organic cation - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as precorrins. These are intermediates formed by methylation at one or more of the four rings prior to the formation of the macrocyclic corrin ring.

External Descriptors

Not available

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