Compound Identification
SMILES
CCOC(=O)C1=CC=C(NC(=O)C2CC(O)CN2S(=O)(=O)C2=CC=C(C)C=C2)C=C1
InChIKey
InChIKey=ASMGZJLQDDGPQC-UHFFFAOYSA-N
Formula
C21H24N2O6S
Mass
432.49
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Benzoic acids and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Acylaminobenzoic acid and derivatives
Alternative Parents
Proline and derivatives N,N-disubstituted p-toluenesulfonamides Alpha amino acid amides Benzenesulfonamides Benzoic acid esters Anilides Benzenesulfonyl compounds Pyrrolidinecarboxamides N-arylamides Benzoyl derivatives Organosulfonamides Sulfonyls Secondary alcohols Secondary carboxylic acid amides Carboxylic acid esters Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
N,n-disubstituted p-toluenesulfonamide - Acylaminobenzoic acid or derivatives - Proline or derivatives - Alpha-amino acid amide - P-toluenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonamide - Benzoate ester - Tosyl compound - Benzenesulfonyl group - Anilide - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Benzoyl - N-arylamide - Toluene - Organosulfonic acid amide - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Pyrrolidine - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid ester - Carboxamide group - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Alcohol - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.
External Descriptors
Not available