Structure Information
Structure

Compound Identification

SMILES

CC1(C)C(N(O)C(=O)NC2=CC(Cl)=CC=C2)N(C(=O)N1CCCCC(=O)NN=CC1=CC(=CC=C1)[N+]([O-])=O)C1=CC(Cl)=CC=C1

InChIKey

InChIKey=MHLSGAYSFCJSFC-UHFFFAOYSA-N

Formula

C30H31Cl2N7O6

Mass

656.52

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Azolidines

Subclass

Imidazolidines

Intermediate Tree Nodes

Not available

Direct Parent

Phenylimidazolidines

Alternative Parents

N-phenylureas Nitrobenzenes Nitroaromatic compounds Chlorobenzenes Imidazolidinones Aryl chlorides Ureas Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Carboxylic acids and derivatives Azacyclic compounds Organic zwitterions Organic salts Organic oxides Organonitrogen compounds Hydrocarbon derivatives Carbonyl compounds Organochlorides

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Phenylimidazolidine - N-phenylurea - Nitrobenzene - Nitroaromatic compound - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Imidazolidinone - Benzenoid - C-nitro compound - Organic nitro compound - Urea - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organic oxoazanium - Carboxylic acid derivative - Organic nitrogen compound - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as phenylimidazolidines. These are polycyclic compounds containing an imidazoline substituted by a phenyl group.

External Descriptors

Not available

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