Compound Identification
SMILES
CCCCOC(=O)C1=C(N)OC(C)=C(C(=O)OC(C)C)C11C(=O)NC2=C1C=C(Br)C=C2
InChIKey
InChIKey=HKFPEJUEKNGQPK-UHFFFAOYSA-N
Formula
C22H25BrN2O6
Mass
493.354
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Indoles and derivatives
- Subclass Indolines
-
Class
Indoles and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Indoles and derivatives
Subclass
Indolines
Intermediate Tree Nodes
Not available
Direct Parent
Indolines
Alternative Parents
Pyrans Aryl bromides Benzenoids Dicarboxylic acids and derivatives Vinylogous esters Vinylogous amides Enoate esters Secondary carboxylic acid amides Ketene acetals Lactams Oxacyclic compounds Azacyclic compounds Organobromides Organonitrogen compounds Carbonyl compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Dihydroindole - Aryl bromide - Aryl halide - Dicarboxylic acid or derivatives - Pyran - Benzenoid - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous amide - Vinylogous ester - Carboxamide group - Carboxylic acid ester - Ketene acetal or derivatives - Lactam - Secondary carboxylic acid amide - Oxacycle - Carboxylic acid derivative - Azacycle - Organonitrogen compound - Organobromide - Organohalogen compound - Organic oxygen compound - Organic oxide - Organopnictogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as indolines. These are compounds containing an indole moiety, which consists of pyrrolidine ring fused to benzene to form 2,3-dihydroindole.
External Descriptors
Not available