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Details

Stereochemistry RACEMIC
Molecular Formula C25H32N2O
Molecular Weight 376.5344
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-ALLYLFENTANYL, CIS-(±)-

SMILES

CCC(=O)N([C@@H]1CCN(CCC2=CC=CC=C2)C[C@@H]1CC=C)C3=CC=CC=C3

InChI

InChIKey=BZXKQFFMDLTPJL-LADGPHEKSA-N
InChI=1S/C25H32N2O/c1-3-11-22-20-26(18-16-21-12-7-5-8-13-21)19-17-24(22)27(25(28)4-2)23-14-9-6-10-15-23/h3,5-10,12-15,22,24H,1,4,11,16-20H2,2H3/t22-,24+/m0/s1

HIDE SMILES / InChI

Approval Year

Patents

Patents

Name Type Language
3-ALLYLFENTANYL, CIS-(±)-
Common Name English
(±)-CIS-3-ALLYLFENTANYL
Preferred Name English
PROPANAMIDE, N-PHENYL-N-((3R,4S)-1-(2-PHENYLETHYL)-3-(2-PROPEN-1-YL)-4-PIPERIDINYL)-, REL-
Systematic Name English
3-ALLYLFENTANYL
Common Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
Code System Code Type Description
CAS
82208-84-2
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
PUBCHEM
133866
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
PRIMARY
WEB RESOURCE
3-ALLYLFENTANYL
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
PRIMARY
WIKIPEDIA
3-ALLYLFENTANYL
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
PRIMARY
CAS
86151-80-6
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
PRIMARY
FDA UNII
V990X77S2I
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
PRIMARY
EPA CompTox
DTXSID001036753
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
PRIMARY
DRUG BANK
DB09169
Created by admin on Mon Mar 31 23:23:55 GMT 2025 , Edited by admin on Mon Mar 31 23:23:55 GMT 2025
PRIMARY