Structure Information
Structure

Compound Identification

SMILES

CCCN1C(C)=C(C(C2=CC(=CC=C2)[N+]([O-])=O)C(C(=O)NC2=CC=CC=C2Cl)=C1C)C(=O)NC1=CC=CC=C1Cl

InChIKey

InChIKey=BOXXJSUBGMLQOT-UHFFFAOYSA-N

Formula

C30H28Cl2N4O4

Mass

579.48

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Pyridines and derivatives

Subclass

Pyridinecarboxylic acids and derivatives

Intermediate Tree Nodes

Pyridinecarboxamides - Nicotinamides

Direct Parent

N-substituted nicotinamides

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

N-substituted nicotinamide - Nitrobenzene - Anilide - Nitroaromatic compound - N-arylamide - Halobenzene - Dihydropyridine - Chlorobenzene - Hydropyridine - Benzenoid - Aryl halide - Aryl chloride - Monocyclic benzene moiety - Vinylogous amide - Secondary carboxylic acid amide - C-nitro compound - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Organic nitro compound - Carboxamide group - Azacycle - Carboxylic acid derivative - Organic 1,3-dipolar compound - Enamine - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic oxide - Organic oxygen compound - Organic salt - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic zwitterion - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Carbonyl group - Organochloride - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as n-substituted nicotinamides. These are nicotnamides in which the pyridine ring is substituted at position 1.

External Descriptors

Not available

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