Structure Information
Structure

Compound Identification

SMILES

CC1(C)OC2(CC3C(=C)CCC(Br)C3(C)C)C(=O)C3=CC(O)=CC(O)=C3C(=O)C2(Cl)CC1Cl

InChIKey

InChIKey=PVEFIGXLPBGZAX-UHFFFAOYSA-N

Formula

C25H29BrCl2O5

Mass

560.31

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Naphthopyrans

Subclass

Naphthopyranones

Intermediate Tree Nodes

Not available

Direct Parent

Naphthopyranones

Alternative Parents

Naphthoquinones Tetralins Quinones Aryl alkyl ketones 1-hydroxy-2-unsubstituted benzenoids Pyranones and derivatives 1-hydroxy-4-unsubstituted benzenoids Oxanes Vinylogous acids Alpha-chloroketones Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Organochlorides Alkyl chlorides Alkyl bromides Organobromides Organic oxides

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Naphthopyranone - Naphthoquinone - Naphthalene - Tetralin - Quinone - Aryl ketone - Aryl alkyl ketone - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Benzenoid - Pyran - Oxane - Vinylogous acid - Alpha-haloketone - Alpha-chloroketone - Ketone - Oxacycle - Dialkyl ether - Ether - Organic oxygen compound - Organohalogen compound - Alkyl bromide - Organobromide - Organochloride - Organooxygen compound - Alkyl chloride - Alkyl halide - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as naphthopyranones. These are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.

External Descriptors

Not available

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