Structure Information
Structure

Compound Identification

SMILES

CC1=CC(N2CCCC2)=C(F)C=C1C=C1NC(=O)N(CC2=CC=C(C=C2)[N+]([O-])=O)C1=O

InChIKey

InChIKey=SHNIYURGPQKPRX-UHFFFAOYSA-N

Formula

C22H21FN4O4

Mass

424.432

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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 - 1-phenylpyrrolidine - Hydantoin - Nitrobenzene - Nitroaromatic compound - Aniline or substituted anilines - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Halobenzene - Fluorobenzene - Benzenoid - N-acyl-amine - Imidazolidinone - Monocyclic benzene moiety - Pyrrolidine - Pyrrole - Imidazolidine - Dicarboximide - Organic nitro compound - Tertiary aliphatic amine - Tertiary amine - Carbonic acid derivative - C-nitro compound - Azacycle - Fluoroalkene - Haloalkene - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Vinyl halide - Vinyl fluoride - Organic oxoazanium - Enamine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Organofluoride - Organic hyponitrite - Organohalogen compound - Amine - 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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