Compound Identification
SMILES
COC1=CC=C(CC2(C)NC(=O)NC2=O)C=C1
InChIKey
InChIKey=KWLVVXBHGRDQMC-UHFFFAOYSA-N
Formula
C12H14N2O3
Mass
234.255
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Azolidines
-
Subclass
Imidazolidines
-
Level 5
Imidazolidinones
-
Level 6
Imidazolidinediones
- Level 7 Hydantoins
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Level 6
Imidazolidinediones
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Level 5
Imidazolidinones
-
Subclass
Imidazolidines
-
Class
Azolidines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Azolidines
Subclass
Imidazolidines
Intermediate Tree Nodes
Imidazolidinones - Imidazolidinediones
Direct Parent
Hydantoins
Alternative Parents
Amphetamines and derivatives Alpha amino acids and derivatives Phenoxy compounds Methoxybenzenes Anisoles 5-monosubstituted hydantoins N-acyl ureas Alkyl aryl ethers Dicarboximides Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Hydantoin - Alpha-amino acid or derivatives - Amphetamine or derivatives - Phenoxy compound - Anisole - Methoxybenzene - 5-monosubstituted hydantoin - Phenol ether - Alkyl aryl ether - Ureide - N-acyl urea - Monocyclic benzene moiety - Benzenoid - Dicarboximide - Urea - Carbonic acid derivative - Carboxylic acid derivative - Azacycle - Ether - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as hydantoins. These are heterocyclic compounds containing an imidazolidine substituted by ketone group at positions 2 and 4.
External Descriptors
Not available