Compound Identification
SMILES
COC(=O)C(C(=O)OC)C1=C(C=C(C=C1)S(=O)(=O)NC1=CC=CC=C1C)[N+]([O-])=O
InChIKey
InChIKey=AIEWXQKSGYYTHU-UHFFFAOYSA-N
Formula
C18H18N2O8S
Mass
422.41
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Sulfanilides
-
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
Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes Nitroaromatic compounds Toluenes 1,3-dicarbonyl compounds Organosulfonamides Dicarboxylic acids and derivatives Methyl esters Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic salts Organonitrogen compounds Hydrocarbon derivatives Organic oxides Organic cations
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Benzenesulfonamide - Sulfanilide - Nitrobenzene - Benzenesulfonyl group - Nitroaromatic compound - Toluene - Organosulfonic acid amide - 1,3-dicarbonyl compound - Dicarboxylic acid or derivatives - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Methyl ester - Aminosulfonyl compound - C-nitro compound - Organic nitro compound - Carboxylic acid ester - Carboxylic acid derivative - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Carbonyl group - Organic oxygen compound - Organic cation - Aromatic homomonocyclic 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