Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC2=C(C=C1)C(=O)N(CC(=O)NC1=CC=C(Cl)C=C1)C=N2

InChIKey

InChIKey=XZULDZYNZSTXJO-UHFFFAOYSA-N

Formula

C16H11ClN4O4

Mass

358.74

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Diazanaphthalenes

Subclass

Benzodiazines

Intermediate Tree Nodes

Quinazolines

Direct Parent

Quinazolinamines

Alternative Parents

Anilides N-arylamides Nitroaromatic compounds Chlorobenzenes Pyrimidones Aryl chlorides Heteroaromatic compounds Lactams Secondary carboxylic acid amides Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic zwitterions Organochlorides

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Quinazolinamine - Anilide - Nitroaromatic compound - N-arylamide - Chlorobenzene - Halobenzene - Pyrimidone - Aryl chloride - Pyrimidine - Aryl halide - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - C-nitro compound - Lactam - Organic nitro compound - Secondary carboxylic acid amide - Carboxamide group - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organic oxoazanium - Azacycle - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Carbonyl group - Organic zwitterion - Organic salt - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as quinazolinamines. These are heterocyclic aromatic compounds containing a quianazoline moiety substituted by one or more amine groups.

External Descriptors

Not available

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