Compound Identification
SMILES
CCOC(=O)N1[C@@H](CO[Si](C)(C)C(C)(C)C)CC(C1O)C(=O)N(CCC1C(=CCS1(=O)=O)C(=O)N(C)C)CC1=CC=CC=C1
InChIKey
InChIKey=USYPEMXVWCMLDH-YXOOPDRDSA-N
Formula
C31H49N3O8SSi
Mass
651.89
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Pyrrolidines
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Subclass
Pyrrolidine carboxylic acids and derivatives
- Level 5 Pyrrolidinecarboxamides
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Subclass
Pyrrolidine carboxylic acids and derivatives
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Class
Pyrrolidines
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyrrolidines
Subclass
Pyrrolidine carboxylic acids and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Pyrrolidinecarboxamides
Alternative Parents
Pyrrolidine carboxylic acids Benzene and substituted derivatives Trialkylheterosilanes Tertiary carboxylic acid amides Sulfones Dihydrothiophenes Carbamate esters Silyl ethers Organic metalloid salts Azacyclic compounds Alkanolamines Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Pyrrolidine carboxylic acid - Pyrrolidine-3-carboxamide - Monocyclic benzene moiety - Benzenoid - 2,5-dihydrothiophene - Trialkylheterosilane - Sulfone - Tertiary carboxylic acid amide - Carbamic acid ester - Silyl ether - Carboxamide group - Azacycle - Organic metalloid salt - Organoheterosilane - Carboxylic acid derivative - Alkanolamine - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organosilicon compound - Hydrocarbon derivative - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as pyrrolidinecarboxamides. These are pyrrolidines in which the pyrrolidine rings is substituted at one or more positions by a carboxamide group. Pyrrolidine is a five-membered saturated aliphatic heterocycle with one nitrogen atom and four carbon atoms.
External Descriptors
Not available