Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)S(=O)(=O)N(CC(C)C)CC(O)C(CC1=CC=CC=C1)NC(=O)C1=C(C)C(=CC=C1)[N+]([O-])=O

InChIKey

InChIKey=LUYSZMPAZWYKEK-UHFFFAOYSA-N

Formula

C29H35N3O7S

Mass

569.67

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Benzenoids

Class

Benzene and substituted derivatives

Subclass

Phenylbutylamines

Intermediate Tree Nodes

Not available

Direct Parent

Phenylbutylamines

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

Phenylbutylamine - Benzenesulfonamide - Amphetamine or derivatives - Nitrobenzene - Benzoic acid or derivatives - Nitrotoluene - Benzamide - Toluamide - O-toluamide - Benzenesulfonyl group - Methoxybenzene - Phenoxy compound - Phenol ether - Benzoyl - Anisole - Nitroaromatic compound - Alkyl aryl ether - Toluene - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Secondary carboxylic acid amide - Secondary alcohol - Organic nitro compound - Carboxamide group - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Ether - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic salt - Organic zwitterion - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Organic oxygen compound - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as phenylbutylamines. These are compounds containing a phenylbutylamine moiety, which consists of a phenyl group substituted at the fourth carbon by an butan-1-amine.

External Descriptors

Not available

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