Compound Identification
SMILES
CC1=CC=C(C=C1)S(=O)(=O)N1CC(C[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)C=C1C1=CC=CC=C1
InChIKey
InChIKey=ITMPOBVXOGHSEF-UHFFFAOYSA-N
Formula
C34H37NO2SSi
Mass
551.82
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Benzenoids
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Class
Benzene and substituted derivatives
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Subclass
Toluenes
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Level 5
Tosyl compounds
- Level 6 P-toluenesulfonamides
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Level 5
Tosyl compounds
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Subclass
Toluenes
-
Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Toluenes
Intermediate Tree Nodes
Tosyl compounds - P-toluenesulfonamides
Direct Parent
N,N-disubstituted p-toluenesulfonamides
Alternative Parents
Phenylpyrrolines Benzenesulfonamides Benzenesulfonyl compounds Alkylarylsilanes Organosulfonamides Sulfonyls Pyrroles Organic metalloid salts Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Alkylsilanes
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
N,n-disubstituted p-toluenesulfonamide - 2-phenylpyrroline - Benzenesulfonamide - Benzenesulfonyl group - Alkylarylsilane - Organosulfonic acid amide - Pyrrole - Pyrroline - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic nitrogen compound - Alkylsilane - Organosilicon compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organosulfur compound - Organonitrogen compound - Organic metalloid moeity - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as n,n-disubstituted p-toluenesulfonamides. These are p-toluenesulfonamide derivatives in which the sulfonamide moiety is N,N-disubstituted.
External Descriptors
Not available