Structure Information
Structure

Compound Identification

SMILES

Cl.Cl.CC(CCN1CCOCC1)C(=O)OC1=CC(=CC2=C1C1=C(CCN(CC#C)C1)C(C)(C)O2)C(C)CCCC1=CC=C(F)C=C1

InChIKey

InChIKey=FQVOOLNJVTUCCO-UHFFFAOYSA-N

Formula

C37H49Cl2FN2O4

Mass

675.71

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Benzopyrans

Subclass

1-benzopyrans

Intermediate Tree Nodes

Not available

Direct Parent

Chromenopyridines

Alternative Parents

2,2-dimethyl-1-benzopyrans Phenol esters Alkyl aryl ethers Fatty acid esters Fluorobenzenes Morpholines Aryl fluorides Trialkylamines Amino acids and derivatives Carboxylic acid esters Oxacyclic compounds Acetylides Monocarboxylic acids and derivatives Azacyclic compounds Dialkyl ethers Organic oxides Carbonyl compounds Hydrochlorides Organofluorides Hydrocarbon derivatives

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Chromenopyridine - 2,2-dimethyl-1-benzopyran - Phenol ester - Alkyl aryl ether - Fatty acid ester - Fluorobenzene - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Morpholine - Oxazinane - Amino acid or derivatives - Carboxylic acid ester - Tertiary aliphatic amine - Tertiary amine - Acetylide - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Dialkyl ether - Azacycle - Oxacycle - Ether - Organooxygen compound - Hydrochloride - Hydrocarbon derivative - Amine - Organic nitrogen compound - Carbonyl group - Organic oxide - Organohalogen compound - Organic oxygen compound - Organofluoride - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as chromenopyridines. These are aromatic heterocyclic compounds structurally characterized by a pyridine ring fused to a chromene moiety.

External Descriptors

Not available

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