Structure Information
Structure

Compound Identification

SMILES

OCCCCC1C=C2C3C(C1CCCCO)C1=C(OC3(OCC=C)C(CC2=NOC2CCCCO2)N(CC2=CC=C(F)C=C2)C(=O)C=CC2=CC=C(C=C2)[N+]([O-])=O)C=CC(OCC=C)=C1

InChIKey

InChIKey=DUTIUQCUFVQGOF-UHFFFAOYSA-N

Formula

C51H60FN3O10

Mass

894.05

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Benzopyrans

Subclass

1-benzopyrans

Intermediate Tree Nodes

Dibenzopyrans

Direct Parent

Xanthenes

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Xanthene - Cinnamic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Styrene - Alkyl aryl ether - Fluorobenzene - Ketal - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Oxane - Benzenoid - Tertiary carboxylic acid amide - Organic nitro compound - Oxime ether - Carboxamide group - C-nitro compound - Organic 1,3-dipolar compound - Oxacycle - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Acetal - Carboxylic acid derivative - Organic oxoazanium - Ether - Organic salt - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organohalogen compound - Organic oxygen compound - Organofluoride - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Alcohol - Organooxygen compound - Primary alcohol - Organic zwitterion - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as xanthenes. These are polycyclic aromatic compounds containing a xanthene moiety, which consists of two benzene rings joined to each other by a pyran ring.

External Descriptors

Not available

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