Compound Identification
SMILES
CC(=O)NC1=CC=C(C=C1)S(=O)(=O)C1=CC=C(S1)[N+]([O-])=O
InChIKey
InChIKey=NROXJWJDZNNZTP-UHFFFAOYSA-N
Formula
C12H10N2O5S2
Mass
326.34
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Benzenoids
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Class
Benzene and substituted derivatives
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Subclass
Anilides
- Level 5 Acetanilides
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Subclass
Anilides
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Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Anilides
Intermediate Tree Nodes
Not available
Direct Parent
Acetanilides
Alternative Parents
2-nitrothiophenes N-acetylarylamines Benzenesulfonyl compounds Nitroaromatic compounds 2,5-disubstituted thiophenes Sulfones Acetamides Heteroaromatic compounds Secondary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic zwitterions Organopnictogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Acetanilide - Benzenesulfonyl group - Nitrothiophene - 2-nitrothiophene - N-acetylarylamine - N-arylamide - Nitroaromatic compound - 2,5-disubstituted thiophene - Thiophene - Sulfone - Heteroaromatic compound - Acetamide - Sulfonyl - Secondary carboxylic acid amide - Organic nitro compound - C-nitro compound - Carboxamide group - Carboxylic acid derivative - Organic oxoazanium - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Organic zwitterion - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as acetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group.
External Descriptors
Not available