Structure Information
Structure

Compound Identification

SMILES

CC(=C)C(O)CC1=C2O[C@]34[C@H]5C[C@H](C=C3C(=O)C2=C(O)C2=C1OC(C)(C)C=C2)C(=O)[C@@]4(C\C=C(\C)C(O)=O)OC5(C)C

InChIKey

InChIKey=QQVYMSAUAKNMII-FNBOYNTASA-N

Formula

C33H36O9

Mass

576.642

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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 2,2-dimethyl-1-benzopyrans Chromones Aromatic monoterpenoids Aryl ketones Phenols Oxepanes Alkyl aryl ethers Cyclohexenones Vinylogous acids Oxolanes Secondary alcohols Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Organic oxides Hydrocarbon derivatives

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyranoxanthone - Pyranochromene - 2,2-dimethyl-1-benzopyran - Chromone - Aromatic monoterpenoid - Monoterpenoid - Aryl ketone - Alkyl aryl ether - Cyclohexenone - Oxepane - Phenol - Benzenoid - Oxolane - Vinylogous acid - Secondary alcohol - Ketone - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Organic oxygen compound - Organic oxide - Alcohol - Carbonyl group - Hydrocarbon derivative - Organooxygen compound - 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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