Structure Information
Structure

Compound Identification

SMILES

COC1=C2C(=O)C3=C(OC2=C2[C@@H](OC(=O)C45CC[C@@](C)(C(=O)O4)C5(C)C)[C@@H](OC(=O)C45CC[C@@](C)(C(=O)O4)C5(C)C)C(C)(C)OC2=C1)C=C(C)C=C3

InChIKey

InChIKey=VRVWUIMYYASGCX-BSQDUVTCSA-N

Formula

C40H44O12

Mass

716.78

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Benzopyrans

Subclass

1-benzopyrans

Intermediate Tree Nodes

Dibenzopyrans - Xanthenes - Xanthones

Direct Parent

Pyranoxanthones

Alternative Parents

Pyranochromenes Tetracarboxylic acids and derivatives 2,2-dimethyl-1-benzopyrans Chromones Anisoles Pyranones and derivatives Alkyl aryl ethers Delta valerolactones Oxanes Gamma butyrolactones Vinylogous esters Oxolanes Heteroaromatic compounds Carboxylic acid esters Oxacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyranoxanthone - Pyranochromene - Tetracarboxylic acid or derivatives - 2,2-dimethyl-1-benzopyran - Chromone - Anisole - Phenol ether - Alkyl aryl ether - Delta valerolactone - Delta_valerolactone - Pyranone - Benzenoid - Gamma butyrolactone - Oxane - Pyran - Vinylogous ester - Oxolane - Heteroaromatic compound - Lactone - Carboxylic acid ester - Oxacycle - Ether - Carboxylic acid derivative - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyranoxanthones. These are organic aromatic compounds containing a pyran or a hydrogenated derivative fused to a xanthone ring system.

External Descriptors

Not available

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