Compound Identification
SMILES
CCCCN(CC)S(=O)(=O)CCC(=O)N[C@@H](CC1=CC(F)=CC(F)=C1)[C@H](O)CNCC1=CC=CC(CC)=C1
InChIKey
InChIKey=GWKMXQREPRGSEN-RRPNLBNLSA-N
Formula
C28H41F2N3O4S
Mass
553.71
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Phenylbutylamines
-
Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Phenylbutylamines
Intermediate Tree Nodes
Not available
Direct Parent
Phenylbutylamines
Alternative Parents
Amphetamines and derivatives Benzylamines Phenylmethylamines Aralkylamines Fluorobenzenes Organic sulfonamides Aryl fluorides Organosulfonamides Aminosulfonyl compounds Amino acids and derivatives Secondary alcohols 1,2-aminoalcohols Secondary carboxylic acid amides Dialkylamines Organic oxides Hydrocarbon derivatives Carbonyl compounds Organofluorides
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Phenylbutylamine - Amphetamine or derivatives - Benzylamine - Phenylmethylamine - Fluorobenzene - Halobenzene - Aralkylamine - Aryl fluoride - Aryl halide - Organosulfonic acid amide - Organic sulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Amino acid or derivatives - 1,2-aminoalcohol - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Secondary aliphatic amine - Carboxylic acid derivative - Secondary amine - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Alcohol - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as phenylbutylamines. These are compounds containing a phenylbutylamine moiety, which consists of a phenyl group substituted at the fourth carbon by an butan-1-amine.
External Descriptors
Not available