Structure Information
Structure

Compound Identification

SMILES

CC1=C(CN2CCOCC2)C(SC2=CC(C)=CC(C)=C2)=C(I)C(=O)N1

InChIKey

InChIKey=BUKGTIWMEIGXAH-UHFFFAOYSA-N

Formula

C19H23IN2O2S

Mass

470.37

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organosulfur compounds

Class

Thioethers

Subclass

Aryl thioethers

Intermediate Tree Nodes

Not available

Direct Parent

Diarylthioethers

Alternative Parents

m-Xylenes Thiophenol ethers Aralkylamines Pyridinones Dihydropyridines Methylpyridines Vinylogous thioesters Aryl iodides Morpholines Heteroaromatic compounds Trialkylamines Lactams Sulfenyl compounds Oxacyclic compounds Azacyclic compounds Dialkyl ethers Organopnictogen compounds Organoiodides Hydrocarbon derivatives Organic oxides

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Diarylthioether - Thiophenol ether - M-xylene - Xylene - Pyridinone - Dihydropyridine - Methylpyridine - Aralkylamine - Aryl halide - Morpholine - Oxazinane - Vinylogous thioester - Hydropyridine - Pyridine - Monocyclic benzene moiety - Benzenoid - Aryl iodide - Heteroaromatic compound - Lactam - Tertiary amine - Tertiary aliphatic amine - Organoheterocyclic compound - Azacycle - Sulfenyl compound - Dialkyl ether - Ether - Oxacycle - Organic nitrogen compound - Organohalogen compound - Amine - Hydrocarbon derivative - Organoiodide - Organic oxide - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as diarylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two aryl groups.

External Descriptors

Not available

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