Compound Identification
SMILES
CN1C2=C3C=CC(C)(C)OC3=CC(O)=C2C(=O)C2=C1C(O)=C(C(C)=O)C(=O)C=C2
InChIKey
InChIKey=JICUMVAAEDQPAI-UHFFFAOYSA-N
Formula
C22H19NO6
Mass
393.395
Taxonomic Classification
Taxonomy Tree
-
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
-
Superclass
Organoheterocyclic compounds
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 Hydroquinolones Hydroquinolines Tropones Aryl alkyl ketones 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Pyridines and derivatives Heteroaromatic compounds Vinylogous amides Vinylogous acids Cyclic ketones Azacyclic compounds Oxacyclic compounds Organonitrogen compounds Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Chromenopyridine - 2,2-dimethyl-1-benzopyran - Dihydroquinolone - Dihydroquinoline - Quinoline - Aryl alkyl ketone - Aryl ketone - Tropone - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Pyridine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Vinylogous acid - Ketone - Cyclic ketone - Ether - Oxacycle - Azacycle - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen 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