Compound Identification
SMILES
CS(=O)(=O)N[C@@H]1OC=CN1[C@@H](CC1=CC(F)=CC(F)=C1)[C@H](O)CNCC1=CC(=CC=C1)C#C
InChIKey
InChIKey=AMALPNRTYHMALW-ZRBLBEILSA-N
Formula
C23H25F2N3O4S
Mass
477.53
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 Phenylmethylamines Benzylamines Aralkylamines Fluorobenzenes Organosulfonamides Aryl fluorides Organic sulfonamides Aminosulfonyl compounds Oxazolines 1,2-aminoalcohols Secondary alcohols Orthocarboxylic acid derivatives Azacyclic compounds Acetylides Oxacyclic compounds Dialkylamines Organofluorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenylbutylamine - Amphetamine or derivatives - Benzylamine - Phenylmethylamine - Fluorobenzene - Halobenzene - Aralkylamine - Aryl halide - Aryl fluoride - Organosulfonic acid amide - Organic sulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Oxazoline - 1,2-aminoalcohol - Orthocarboxylic acid derivative - Secondary alcohol - Secondary amine - Secondary aliphatic amine - Organoheterocyclic compound - Acetylide - Azacycle - Oxacycle - Hydrocarbon derivative - Organohalogen compound - Alcohol - Organofluoride - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organic oxide - Amine - Aromatic heteromonocyclic 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