Compound Identification
SMILES
COC1=CC=C(C=C1)S(=O)(=O)N(CC(=O)NC1=CC=C(C=C1)S(=O)(=O)N1CCCCC1)C1=CC=C(Cl)C=C1
InChIKey
InChIKey=NNXREDKDPMEFQW-UHFFFAOYSA-N
Formula
C26H28ClN3O6S2
Mass
578.1
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
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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
Alpha amino acids and derivatives Benzenesulfonamides Anilides Benzenesulfonyl compounds Phenoxy compounds Anisoles N-arylamides Methoxybenzenes Alkyl aryl ethers Chlorobenzenes Piperidines Organosulfonamides Aryl chlorides Aminosulfonyl compounds Secondary carboxylic acid amides Azacyclic compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Sulfanilide - Benzenesulfonamide - Alpha-amino acid or derivatives - Anilide - Benzenesulfonyl group - Methoxybenzene - Phenoxy compound - N-arylamide - Phenol ether - Anisole - Alkyl aryl ether - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Organosulfonic acid amide - Piperidine - Aminosulfonyl compound - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Organooxygen compound - Organic oxide - Organosulfur compound - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organohalogen compound - Organochloride - 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