Compound Identification
SMILES
CC1(C)[C@]2(C)CC[C@@]1(OC2=O)C(=O)NC1=C(Br)C=C(F)C=C1
InChIKey
InChIKey=NWYTVZOHIKJKTI-HZPDHXFCSA-N
Formula
C16H17BrFNO3
Mass
370.218
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 Bromobenzenes Delta valerolactones Fluorobenzenes Pyrans Oxanes Aryl bromides Aryl fluorides Gamma butyrolactones Oxolanes Secondary carboxylic acid amides Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organic oxides Carbonyl compounds Organobromides Organofluorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Anilide - N-arylamide - Bromobenzene - Delta valerolactone - Fluorobenzene - Halobenzene - Delta_valerolactone - Aryl bromide - Aryl fluoride - Aryl halide - Gamma butyrolactone - Pyran - Oxane - Oxolane - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Lactone - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxide - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organohalogen compound - Organobromide - Organofluoride - Aromatic heteropolycyclic 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