Compound Identification
SMILES
CC(=O)NC1=CC=C(SCC2CC(OC(O2)C2=CC=C(NS(=O)(=O)C3=CC=CC=C3)C=C2)C2=CC=C(CO)C=C2)C=C1
InChIKey
InChIKey=RCYBZBUQYYBKKC-UHFFFAOYSA-N
Formula
C32H32N2O6S2
Mass
604.74
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
Acetanilides Benzenesulfonamides Benzenesulfonyl compounds N-acetylarylamines Thiophenol ethers Benzyl alcohols Alkylarylthioethers 1,3-dioxanes Organosulfonamides Acetamides Aminosulfonyl compounds Secondary carboxylic acid amides Oxacyclic compounds Acetals Sulfenyl compounds Organic oxides Organopnictogen compounds Aromatic alcohols Primary alcohols Carbonyl compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Acetanilide - Benzenesulfonamide - Sulfanilide - N-acetylarylamine - Benzenesulfonyl group - Anilide - Aryl thioether - Benzyl alcohol - Thiophenol ether - N-arylamide - Alkylarylthioether - Meta-dioxane - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Acetamide - Aminosulfonyl compound - Carboxamide group - Secondary carboxylic acid amide - Thioether - Organoheterocyclic compound - Oxacycle - Acetal - Sulfenyl compound - Carboxylic acid derivative - Alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic alcohol - Organic nitrogen 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