Compound Identification
SMILES
Cl.CCC(C)N1CN(C2=CC=CC=C2)C2(CCN(CCCC3(OCCO3)C3=CC=C(F)C=C3)CC2)C1=O
InChIKey
InChIKey=DGIHAGDZGFDIBK-UHFFFAOYSA-N
Formula
C29H39ClFN3O3
Mass
532.1
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
Phenylimidazolidines Azaspirodecane derivatives Alpha amino acids and derivatives Dialkylarylamines Aniline and substituted anilines Fluorobenzenes Ketals Aralkylamines Piperidines Imidazolidinones Aryl fluorides Tertiary carboxylic acid amides 1,3-dioxolanes Trialkylamines Lactams Oxacyclic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Hydrochlorides Organic oxides Organofluorides Organopnictogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Phenylimidazolidine - Phenylbutylamine - Alpha-amino acid or derivatives - Azaspirodecane - Dialkylarylamine - Aniline or substituted anilines - Fluorobenzene - Aralkylamine - Ketal - Halobenzene - Imidazolidinone - Aryl halide - Piperidine - Aryl fluoride - Meta-dioxolane - Tertiary carboxylic acid amide - Imidazolidine - Amino acid or derivatives - Lactam - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Oxacycle - Organoheterocyclic compound - Acetal - Azacycle - Organic nitrogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrochloride - Hydrocarbon derivative - Organic oxide - Amine - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic 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