Compound Identification
SMILES
CC1CC2=C(O1)C=CC(=C2)C(\O)=C1\C(N(CCN(C)C)C(=O)C1=O)C1=CC=C(C)O1
InChIKey
InChIKey=CHMSLHYHVMBALW-XUTLUUPISA-N
Formula
C23H26N2O5
Mass
410.47
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
- Class Coumarans
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Coumarans
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Coumarans
Alternative Parents
Alkyl aryl ethers Pyrrolidine-3-ones Pyrrolidine-2-ones Benzenoids N-alkylpyrrolidines Vinylogous acids Tertiary carboxylic acid amides Furans Heteroaromatic compounds Trialkylamines Amino acids and derivatives Cyclic ketones Lactams Azacyclic compounds Enols Oxacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Coumaran - Alkyl aryl ether - Pyrrolidone - 2-pyrrolidone - 3-pyrrolidone - N-alkylpyrrolidine - Benzenoid - Furan - Pyrrolidine - Tertiary carboxylic acid amide - Heteroaromatic compound - Vinylogous acid - Cyclic ketone - Carboxamide group - Ketone - Lactam - Tertiary amine - Amino acid or derivatives - Tertiary aliphatic amine - Azacycle - Oxacycle - Ether - Enol - Carboxylic acid derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as coumarans. These are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring.
External Descriptors
Not available