Structure Information
Structure

Compound Identification

SMILES

CCOCCOCCN1C2=CC(NC(C)=O)=C(C=C2C(C)CC1(C)C)N=NC1=C(C=C(C=C1Br)[N+]([O-])=O)[N+]([O-])=O

InChIKey

InChIKey=DZLSCJIHAREOKL-UHFFFAOYSA-N

Formula

C26H33BrN6O7

Mass

621.489

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Quinolines and derivatives

Subclass

Hydroquinolines

Intermediate Tree Nodes

Not available

Direct Parent

Hydroquinolines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Tetrahydroquinoline - N-acetylarylamine - Nitrobenzene - Nitroaromatic compound - Dialkylarylamine - Tertiary aliphatic/aromatic amine - N-arylamide - Bromobenzene - Halobenzene - Aralkylamine - Aryl bromide - Aryl halide - Monocyclic benzene moiety - Benzenoid - Acetamide - Amino acid or derivatives - Azo compound - Carboxamide group - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Tertiary amine - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxoazanium - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organohalogen compound - Carbonyl group - Organic oxide - Amine - Organic salt - Organopnictogen compound - Organobromide - Organic zwitterion - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.

External Descriptors

Not available

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