Compound Identification
SMILES
CN1C=C(N=C1C)S(=O)(=O)N(CCCN1C(=O)CCC1=O)CC1=CC=CC=C1
InChIKey
InChIKey=POJYKJCAEOHAAY-UHFFFAOYSA-N
Formula
C19H24N4O4S
Mass
404.49
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Azoles
-
Subclass
Imidazoles
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Level 5
Substituted imidazoles
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Level 6
Trisubstituted imidazoles
- Level 7 1,2,4-trisubstituted imidazoles
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Level 6
Trisubstituted imidazoles
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Level 5
Substituted imidazoles
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Subclass
Imidazoles
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Class
Azoles
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Azoles
Subclass
Imidazoles
Intermediate Tree Nodes
Substituted imidazoles - Trisubstituted imidazoles
Direct Parent
1,2,4-trisubstituted imidazoles
Alternative Parents
Pyrrolidine-2-ones Organosulfonamides N-substituted imidazoles N-substituted carboxylic acid imides N-alkylpyrrolidines Benzene and substituted derivatives Heteroaromatic compounds Dicarboximides Aminosulfonyl compounds Lactams Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
1,2,4-trisubstituted-imidazole - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - N-substituted imidazole - Pyrrolidone - 2-pyrrolidone - Organosulfonic acid amide - N-alkylpyrrolidine - Benzenoid - Sulfonyl - Carboxylic acid imide - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Pyrrolidine - Dicarboximide - Aminosulfonyl compound - Lactam - Carboxylic acid derivative - Azacycle - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as 1,2,4-trisubstituted imidazoles. These are imidazoles in which the imidazole ring is substituted at positions 1, 2, and 3.
External Descriptors
Not available