Compound Identification
SMILES
COC1=CC2=C(C=C1)C1=C(CN(CC3=CC(Cl)=C(Cl)C=C3)CC1)C(=O)O2
InChIKey
InChIKey=CDPWDOLVSDDBEM-UHFFFAOYSA-N
Formula
C20H17Cl2NO3
Mass
390.26
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
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Class
Benzopyrans
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Subclass
1-benzopyrans
- Level 5 Chromenopyridines
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Subclass
1-benzopyrans
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Class
Benzopyrans
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Benzopyrans
Subclass
1-benzopyrans
Intermediate Tree Nodes
Not available
Direct Parent
Chromenopyridines
Alternative Parents
Coumarins and derivatives Phenylmethylamines Anisoles Dichlorobenzenes Benzylamines Pyranones and derivatives Alkyl aryl ethers Aralkylamines Aryl chlorides Heteroaromatic compounds Trialkylamines Lactones Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Organochlorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Chromenopyridine - Coumarin - Anisole - Benzylamine - 1,2-dichlorobenzene - Phenol ether - Phenylmethylamine - Alkyl aryl ether - Chlorobenzene - Aralkylamine - Halobenzene - Pyranone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Pyran - Heteroaromatic compound - Tertiary amine - Tertiary aliphatic amine - Lactone - Ether - Azacycle - Oxacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Organonitrogen compound - Organooxygen compound - Organohalogen compound - Organochloride - 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