Compound Identification
SMILES
COC1=CC=CC(=C1)N1C(=O)CC(N(NC(=O)C2=CC(OC)=C(OC)C=C2)C(=O)C=CC)C1=O
InChIKey
InChIKey=FCDGIDQSNCVIPM-UHFFFAOYSA-N
Formula
C24H25N3O7
Mass
467.478
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Pyrrolidines
- Subclass Phenylpyrrolidines
-
Class
Pyrrolidines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyrrolidines
Subclass
Phenylpyrrolidines
Intermediate Tree Nodes
Not available
Direct Parent
Phenylpyrrolidines
Alternative Parents
Alpha amino acids and derivatives Dimethoxybenzenes Benzoic acids and derivatives Methoxyanilines Benzoyl derivatives Anisoles Phenoxy compounds Alkyl aryl ethers N-substituted carboxylic acid imides Pyrrolidine-2-ones Pyrroles Dicarboximides Lactams Carboxylic acid hydrazides Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organonitrogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
1-phenylpyrrolidine - Alpha-amino acid or derivatives - Dimethoxybenzene - O-dimethoxybenzene - Methoxyaniline - Benzoic acid or derivatives - Benzoyl - Phenol ether - Phenoxy compound - Anisole - Methoxybenzene - Alkyl aryl ether - 2-pyrrolidone - Pyrrolidone - Benzenoid - Carboxylic acid imide, n-substituted - Monocyclic benzene moiety - Pyrrole - Carboxylic acid imide - Dicarboximide - Lactam - Carboxylic acid hydrazide - Azacycle - Carboxylic acid derivative - Ether - Carbonyl group - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organic oxide - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as phenylpyrrolidines. These are polycyclic aromatic compounds containing a benzene ring linked to a pyrrolidine ring through a CC or CN bond. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
External Descriptors
Not available