Structure Information
Structure

Compound Identification

SMILES

C\C(=C/CC12OC(C)(C)C3CC(C=C4C(=O)C5=C(OC134)C(CCC(C)(C)Cl)=C1OC3(C)CCC(C(C3)C1=C5O)C1(C)CO1)C2=O)C(O)=O

InChIKey

InChIKey=BMPKGNCYXQRUMA-QGMBQPNBSA-N

Formula

C38H45ClO9

Mass

681.22

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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 Chromones Aromatic monoterpenoids Aryl ketones Phenols Oxepanes Alkyl aryl ethers Cyclohexenones Vinylogous acids Oxolanes Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Dialkyl ethers Epoxides Organochlorides Hydrocarbon derivatives Organic oxides Alkyl chlorides

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyranoxanthone - Pyranochromene - Chromone - Aromatic monoterpenoid - Monoterpenoid - Aryl ketone - Alkyl aryl ether - Cyclohexenone - Phenol - Oxepane - Benzenoid - Vinylogous acid - Oxolane - Ketone - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Oxirane - Ether - Oxacycle - Monocarboxylic acid or derivatives - Alkyl halide - Hydrocarbon derivative - Alkyl chloride - Organic oxide - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organohalogen compound - Organochloride - 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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