Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC(Cl)=C(NC(=O)CN2CCN(CC2)S(=O)(=O)C2=CC=CC=C2)C=C1

InChIKey

InChIKey=JUALHHMPAUYVLD-UHFFFAOYSA-N

Formula

C18H19ClN4O5S

Mass

438.88

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Subclass

Amino acids, peptides, and analogues

Intermediate Tree Nodes

Amino acids and derivatives - Alpha amino acids and derivatives

Direct Parent

Alpha amino acid amides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Alpha-amino acid amide - N-piperazineacetamide - Benzenesulfonamide - Nitrobenzene - Anilide - Benzenesulfonyl group - Nitroaromatic compound - N-arylamide - Chlorobenzene - N-alkylpiperazine - Halobenzene - Aryl chloride - 1,4-diazinane - Piperazine - Benzenoid - Monocyclic benzene moiety - Organosulfonic acid amide - Aryl halide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary aliphatic amine - Tertiary amine - Carboxamide group - Secondary carboxylic acid amide - Organic nitro compound - C-nitro compound - Azacycle - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organosulfur compound - Organic oxygen compound - Organic salt - Amine - Organic nitrogen compound - Carbonyl group - Organic zwitterion - Organic oxide - Organohalogen compound - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids.

External Descriptors

Not available

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