Structure Information
Structure

Compound Identification

SMILES

COC(OC)[C@]1(O)O[C@H]2[C@@H](O)C3=C(C)C=C4C(OC)=C5[C@H](C[C@H](O)C(=O)C5=C(O)C4=C3O[C@@]2(O)[C@@]1(O)CO)O[C@H]1CC(C)(O)[C@H](OC(C)=O)C(C)O1

InChIKey

InChIKey=CQPUGZMZSAGHEF-KZAQPVPCSA-N

Formula

C34H44O18

Mass

740.708

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Naphthopyrans

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Naphthopyrans

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Naphthopyran - Glycosyl compound - 1-naphthol - O-glycosyl compound - Chromane - Benzopyran - Naphthalene - Tetralin - 1-benzopyran - Anisole - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - Pyran - Oxane - Benzenoid - Monosaccharide - Tetrahydrofuran - Tertiary alcohol - Vinylogous acid - Secondary alcohol - Carboxylic acid ester - Hemiacetal - Ketone - Polyol - Oxacycle - Acetal - Carboxylic acid derivative - Ether - Monocarboxylic acid or derivatives - Carbonyl group - Alcohol - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as naphthopyrans. These are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

External Descriptors

Not available

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