Compound Identification
SMILES
COC1=CC(NS(C)(=O)=O)=C(NC2=NC(NC3=C(OC)C=CC(F)=C3)=NC=C2Cl)C=C1
InChIKey
InChIKey=LBDDRPXNZKVVCG-UHFFFAOYSA-N
Formula
C19H19ClFN5O4S
Mass
467.9
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Sulfanilides
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Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Sulfanilides
Intermediate Tree Nodes
Not available
Direct Parent
Sulfanilides
Alternative Parents
Methoxyanilines Phenoxy compounds Anisoles Methoxybenzenes Alkyl aryl ethers Aminopyrimidines and derivatives Fluorobenzenes Halopyrimidines Organosulfonamides Aryl chlorides Aryl fluorides Organic sulfonamides Imidolactams Aminosulfonyl compounds Heteroaromatic compounds Azacyclic compounds Secondary amines Organochlorides Organofluorides Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Sulfanilide - Methoxyaniline - Anisole - Phenoxy compound - Phenol ether - Aniline or substituted anilines - Methoxybenzene - Alkyl aryl ether - Aminopyrimidine - Fluorobenzene - Halobenzene - Halopyrimidine - Organosulfonic acid amide - Organic sulfonic acid amide - Pyrimidine - Imidolactam - Aryl chloride - Aryl fluoride - Aryl halide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Azacycle - Secondary amine - Organoheterocyclic compound - Ether - Organic oxide - Organic nitrogen compound - Amine - Organohalogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.
External Descriptors
Not available