Compound Identification
SMILES
COC[C@H]1CCCN1C(=O)C1=CC(C)=CC(=C1)C(=O)N[C@@H](CC1=CC(F)=CC(F)=C1)[C@@H](O)CNC1(CC1)C1=CC=CC(=C1)C#C
InChIKey
InChIKey=NPJRUOLUVLZQTK-CEUYOYMZSA-N
Formula
C36H39F2N3O4
Mass
615.722
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Phenylbutylamines
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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
N,N-dialkyl-m-toluamides Amphetamines and derivatives Benzamides N-acylpyrrolidines Benzoyl derivatives Fluorobenzenes Aralkylamines Aryl fluorides Tertiary carboxylic acid amides Secondary carboxylic acid amides Secondary alcohols 1,2-aminoalcohols Amino acids and derivatives Acetylides Dialkylamines Dialkyl ethers Azacyclic compounds Organofluorides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Phenylbutylamine - N,n-dialkyl-m-toluamide - Amphetamine or derivatives - Benzoic acid or derivatives - Benzamide - Toluamide - M-toluamide - N-acylpyrrolidine - Benzoyl - Halobenzene - Aralkylamine - Toluene - Fluorobenzene - Aryl halide - Aryl fluoride - Tertiary carboxylic acid amide - Pyrrolidine - Secondary carboxylic acid amide - Secondary alcohol - 1,2-aminoalcohol - Carboxamide group - Amino acid or derivatives - Acetylide - Azacycle - Organoheterocyclic compound - Secondary amine - Carboxylic acid derivative - Dialkyl ether - Secondary aliphatic amine - Ether - Organic oxygen compound - Amine - Alcohol - Organooxygen compound - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organofluoride - Organohalogen compound - 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