Compound Identification
SMILES
CC(=O)C1=C(C)NC(C(=O)NC2=CC=C(OC(F)(F)F)C=C2)=C1C
InChIKey
InChIKey=QKEIFLQYGQKUFW-UHFFFAOYSA-N
Formula
C16H15F3N2O3
Mass
340.302
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
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Subclass
Anilides
- Level 5 Aromatic anilides
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Subclass
Anilides
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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
Aromatic anilides
Alternative Parents
2-heteroaryl carboxamides Aryl alkyl ketones Phenol ethers Pyrrole carboxamides Phenoxy compounds Substituted pyrroles Vinylogous amides Heteroaromatic compounds Trihalomethanes Secondary carboxylic acid amides Azacyclic compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides Organopnictogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Aromatic anilide - 2-heteroaryl carboxamide - Phenol ether - Phenoxy compound - Pyrrole-2-carboxamide - Pyrrole-2-carboxylic acid or derivatives - Aryl ketone - Aryl alkyl ketone - Substituted pyrrole - Pyrrole - Heteroaromatic compound - Vinylogous amide - Carboxamide group - Ketone - Secondary carboxylic acid amide - Trihalomethane - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Alkyl fluoride - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Alkyl halide - Halomethane - Hydrocarbon derivative - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group.
External Descriptors
Not available