Structure Information
Structure

Compound Identification

SMILES

CC1=C(C(=O)OC2=C1C=CC1=C2C(C)=C(C(=O)O1)C1=CC=C(Cl)C=C1)C1=CC=C(Cl)C=C1

InChIKey

InChIKey=JOQZNGXLJHLISE-UHFFFAOYSA-N

Formula

C26H16Cl2O4

Mass

463.31

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Isoflavonoids

Subclass

Pyranoisoflavonoids

Intermediate Tree Nodes

Not available

Direct Parent

Pyranoisoflavonoids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyranoisoflavonoid - Linear 1,7-diphenylheptane skeleton - Isoflav-3-enone skeleton - Pyranocoumarin - Angular pyranocoumarin - Coumarin - Benzopyran - 1-benzopyran - Chlorobenzene - Halobenzene - Pyranone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyran - Heteroaromatic compound - Lactone - Oxacycle - Organoheterocyclic compound - Organic oxide - Organic oxygen compound - Organohalogen compound - Organochloride - Organooxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyranoisoflavonoids. These are isoflavonoids that contain a pyran ring fused to either of the A, B, or C ring of the isoflavonoid skeleton.

External Descriptors

Not available

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