Compound Identification
SMILES
OCC1=CC=C(C=C1)C1CC(CN(CC2=CC=CC=C2)CC2=CC=CC=C2)OC(O1)C1=CC=C(NC(=O)CCCCCCC(O)=O)C=C1
InChIKey
InChIKey=KUVQMHJAYMGZRT-UHFFFAOYSA-N
Formula
C40H46N2O6
Mass
650.816
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Anilides
-
Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Anilides
Intermediate Tree Nodes
Not available
Direct Parent
Anilides
Alternative Parents
Phenylmethylamines Benzyl alcohols Benzylamines N-arylamides Medium-chain fatty acids Aralkylamines Hydroxy fatty acids Amino fatty acids Heterocyclic fatty acids 1,3-dioxanes Fatty amides Trialkylamines Secondary carboxylic acid amides Amino acids Carboxylic acids Monocarboxylic acids and derivatives Acetals Oxacyclic compounds Aromatic alcohols Carbonyl compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds Primary alcohols
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - Benzyl alcohol - Benzylamine - Phenylmethylamine - Medium-chain fatty acid - N-arylamide - Amino fatty acid - Heterocyclic fatty acid - Hydroxy fatty acid - Aralkylamine - Fatty acyl - Fatty acid - Meta-dioxane - Fatty amide - Amino acid - Amino acid or derivatives - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Carboxamide group - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Acetal - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Amine - Primary alcohol - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Alcohol - Aromatic alcohol - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
External Descriptors
Not available