Compound Identification
SMILES
COC1=C(Br)C2=NC(=NN2C(Cl)=N1)S(=O)(=O)NC1=C(Cl)C=CC(C)=C1Cl
InChIKey
InChIKey=YQDGOTZOMSLTAQ-UHFFFAOYSA-N
Formula
C13H9BrCl3N5O3S
Mass
501.56
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
Triazolopyrimidines Dichlorobenzenes Toluenes 2-halopyrimidines Alkyl aryl ethers Organosulfonamides Aryl bromides Aryl chlorides Triazoles Aminosulfonyl compounds Heteroaromatic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organobromides Organochlorides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Sulfanilide - Triazolopyrimidine - 1,3-dichlorobenzene - Alkyl aryl ether - Chlorobenzene - Halobenzene - Halopyrimidine - Toluene - 2-halopyrimidine - Aryl halide - Organosulfonic acid amide - Pyrimidine - Aryl bromide - Aryl chloride - Azole - 1,2,4-triazole - Triazole - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Aminosulfonyl compound - Azacycle - Organoheterocyclic compound - Ether - Organic oxide - Organohalogen compound - Organobromide - Organochloride - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic 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