Compound Identification
SMILES
CC1(C)[C@@]2(C)CC[C@]1(OC2=O)C(=O)NC1=C(Cl)C=C(Cl)C=C1
InChIKey
InChIKey=NTOYAIOKEQADKS-HOTGVXAUSA-N
Formula
C16H17Cl2NO3
Mass
342.22
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
Dichlorobenzenes N-arylamides Delta valerolactones Oxanes Gamma butyrolactones Aryl chlorides Pyrans Oxolanes Carboxylic acid esters Secondary carboxylic acid amides Oxacyclic compounds Monocarboxylic acids and derivatives Organopnictogen compounds Organochlorides Organic oxides Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Anilide - N-arylamide - 1,3-dichlorobenzene - Delta_valerolactone - Halobenzene - Delta valerolactone - Chlorobenzene - Aryl halide - Aryl chloride - Pyran - Oxane - Gamma butyrolactone - Oxolane - Secondary carboxylic acid amide - Carboxamide group - Lactone - Carboxylic acid ester - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Carbonyl group - 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