Compound Identification
SMILES
CC(C)OCCCNC(=O)C1=CC2=C(S1)C=CC(=C2)N(CC1=CN=CN1CC1=CC=C(C=C1)C#N)S(=O)(=O)C1=CC=CC=C1
InChIKey
InChIKey=XLRAKKHXNNMVBB-UHFFFAOYSA-N
Formula
C33H33N5O4S2
Mass
627.78
Taxonomic Classification
Taxonomy Tree
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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
Benzenesulfonamides 1-benzothiophenes Benzenesulfonyl compounds Thiophene carboxamides 2,3,5-trisubstituted thiophenes 2-heteroaryl carboxamides Benzonitriles Organosulfonamides N-substituted imidazoles Heteroaromatic compounds Aminosulfonyl compounds Secondary carboxylic acid amides Nitriles Dialkyl ethers Azacyclic compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Benzenesulfonamide - Sulfanilide - Benzothiophene - 1-benzothiophene - Benzenesulfonyl group - 2-heteroaryl carboxamide - Benzonitrile - Thiophene carboxamide - Thiophene carboxylic acid or derivatives - 2,3,5-trisubstituted thiophene - N-substituted imidazole - Organosulfonic acid amide - Azole - Imidazole - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Heteroaromatic compound - Sulfonyl - Thiophene - Aminosulfonyl compound - Secondary carboxylic acid amide - Carboxamide group - Dialkyl ether - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Nitrile - Carbonitrile - Ether - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Cyanide - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic 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