Compound Identification
SMILES
CN(C)C1=CC=C(C=C1)[N+](\[O-])=C/C1=CC(=O)C2=C(O1)C1=CC=CC=C1C=C2
InChIKey
InChIKey=QXCHXWFFBSZINU-ZVHZXABRSA-N
Formula
C22H18N2O3
Mass
358.397
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Naphthopyrans
- Subclass Naphthopyranones
-
Class
Naphthopyrans
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Naphthopyrans
Subclass
Naphthopyranones
Intermediate Tree Nodes
Not available
Direct Parent
Naphthopyranones
Alternative Parents
Chromones Naphthalenes Dialkylarylamines Aniline and substituted anilines Pyranones and derivatives Heteroaromatic compounds Shiff bases Nitrones Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organooxygen compounds Organic zwitterions Organic salts Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Naphthopyranone - Chromone - Benzopyran - Naphthalene - 1-benzopyran - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Pyranone - Benzenoid - Monocyclic benzene moiety - Pyran - Heteroaromatic compound - Tertiary amine - Nitrone - Shiff base - Oxacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic salt - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organic zwitterion - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as naphthopyranones. These are compounds containing a naphthopyran skeleton where a ring carbon bears a carboxylic acid group. Naphthtopyran is made up of the pyran ring fused to a naphthalene ring system.
External Descriptors
Not available