Compound Identification
SMILES
CC1=NC(=C(OCC(=O)NC2=C(Cl)C=C(F)C=C2)C=C1)[N+]([O-])=O
InChIKey
InChIKey=KRECCDGBGNVMIE-UHFFFAOYSA-N
Formula
C14H11ClFN3O4
Mass
339.71
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
N-arylamides Nitroaromatic compounds Alkyl aryl ethers Chlorobenzenes Fluorobenzenes Methylpyridines Imidolactams Aryl fluorides Aryl chlorides Heteroaromatic compounds Secondary carboxylic acid amides Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic salts Organic zwitterions Organochlorides Organofluorides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - N-arylamide - Nitroaromatic compound - Alkyl aryl ether - Halobenzene - Fluorobenzene - Chlorobenzene - Methylpyridine - Aryl chloride - Imidolactam - Pyridine - Aryl halide - Aryl fluoride - Heteroaromatic compound - Organic nitro compound - C-nitro compound - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Carbonyl group - Hydrocarbon derivative - Organic salt - Organic oxide - Organic oxygen compound - Organohalogen compound - Organic nitrogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic zwitterion - 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