Compound Identification
SMILES
CCS(=O)(=O)OC1=CC(Cl)=CC(OC(=O)C2=CC=C(C=C2)N=C(N)N)=C1
InChIKey
InChIKey=NJAOPEJJXQYQBE-UHFFFAOYSA-N
Formula
C16H16ClN3O5S
Mass
397.83
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Phenylpropanoids and polyketides
- Class Depsides and depsidones
-
Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Depsides and depsidones
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Depsides and depsidones
Alternative Parents
Guanidinobenzoic acids and derivatives Benzoic acid esters Phenol esters Benzoyl derivatives Phenoxy compounds Chlorobenzenes Aryl chlorides Sulfonic acid esters Organosulfonic acid esters Sulfonyls Guanidines Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Organooxygen compounds Organochlorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Depside backbone - Guanidinobenzoic acid or derivatives - Phenol ester - Benzoate ester - Benzoic acid or derivatives - Benzoyl - Phenoxy compound - Chlorobenzene - Halobenzene - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid ester - Sulfonic acid ester - Aryl halide - Aryl chloride - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxylic acid ester - Guanidine - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as depsides and depsidones. These are polycyclic compounds that is either a polyphenolic compound composed of two or more monocyclic aromatic units linked by an ester bond (depside), or a compound containing the depsidone structure (depsidone).
External Descriptors
Not available