Compound Identification
SMILES
CN(C)CCCN(C)C1=C(NC(=O)C2=CC(Br)=CC3=C2OCC3)C=C(C=C1)C(F)(F)F
InChIKey
InChIKey=FLNWOTWGRZQANT-UHFFFAOYSA-N
Formula
C22H25BrF3N3O2
Mass
500.36
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
Trifluoromethylbenzenes 3-halobenzoic acids and derivatives Coumarans Aniline and substituted anilines Dialkylarylamines Alkyl aryl ethers Aryl bromides Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Oxacyclic compounds Organic oxides Organobromides Alkyl fluorides Organofluorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Aromatic anilide - Trifluoromethylbenzene - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Coumaran - Aniline or substituted anilines - Dialkylarylamine - Alkyl aryl ether - Aryl bromide - Aryl halide - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Ether - Alkyl halide - Organobromide - Organohalogen compound - Organofluoride - Organonitrogen compound - Alkyl fluoride - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic 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