Structure Information
Structure

Compound Identification

SMILES

CC1=C(C=CC(=C1)N(CCC#N)CCC#N)C(=NNC1=CC(=CC=C1)[N+]([O-])=O)N=NC(=O)C1=C(O)C=CC(Cl)=C1

InChIKey

InChIKey=KFLYFFYTWGVAIC-UHFFFAOYSA-N

Formula

C27H23ClN8O4

Mass

558.98

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Benzenoids

Class

Benzene and substituted derivatives

Subclass

Benzoic acids and derivatives

Intermediate Tree Nodes

Hydroxybenzoic acid derivatives - Salicylic acid and derivatives

Direct Parent

Salicylamides

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Salicylamide - Nitrobenzene - Tertiary aliphatic/aromatic amine - Nitroaromatic compound - Phenylhydrazine - 4-chlorophenol - Dialkylarylamine - Aniline or substituted anilines - Aminotoluene - Benzoyl - 4-halophenol - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Toluene - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Formazan - Vinylogous acid - Tertiary amine - Azo compound - Organic nitro compound - Amino acid or derivatives - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organic oxoazanium - Hydrazone - Nitrile - Carbonitrile - Organic salt - Organohalogen compound - Organochloride - Hydrocarbon derivative - Amine - Organic oxide - Organonitrogen compound - Cyanide - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Organic zwitterion - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as salicylamides. These are carboxamide derivatives of salicylic acid. Salicylic acid is the ortho-hydroxylated derivative of benzoic acid.

External Descriptors

Not available

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