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Details

Stereochemistry ACHIRAL
Molecular Formula C27H28N2O3
Molecular Weight 428.5228
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Benzodioxole fentanyl

SMILES

O=C(N(C1CCN(CCC2=CC=CC=C2)CC1)C3=CC=CC=C3)C4=CC=C5OCOC5=C4

InChI

InChIKey=ZFAAZMIOHJNKGD-UHFFFAOYSA-N
InChI=1S/C27H28N2O3/c30-27(22-11-12-25-26(19-22)32-20-31-25)29(23-9-5-2-6-10-23)24-14-17-28(18-15-24)16-13-21-7-3-1-4-8-21/h1-12,19,24H,13-18,20H2

HIDE SMILES / InChI

Approval Year

Unknown
149124
Name Type Language
Benzodioxole fentanyl
Common Name English
BENZODIOXOLEFENTANYL
Preferred Name English
1,3-BENZODIOXOLE-5-CARBOXAMIDE, N-PHENYL-N-(1-(2-PHENYLETHYL)-4-PIPERIDINYL)-
Systematic Name English
N-PHENYL-N-(1-(2-PHENYLETHYL)PIPERIDIN-4-YL)-2H-1,3-BENZODIOXOLE-5-CARBOXAMIDE
Systematic Name English
N-PHENYL-N-(1-(2-PHENYLETHYL)-4-PIPERIDINYL)-1,3-BENZODIOXOLE-5-CARBOXAMIDE
Systematic Name English
N-(1-PHENETHYLPIPERIDIN-4-YL)-N-PHENYLBENZO(D)(1,3)DIOXOLE-5-CARBOXAMIDE
Systematic Name English
BENZODIOXOLE FENTANYL [NFLIS-DRUG]
Common Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Wed Apr 02 05:30:24 GMT 2025 , Edited by admin on Wed Apr 02 05:30:24 GMT 2025
Code System Code Type Description
CAYMAN
20858
Created by admin on Wed Apr 02 05:30:24 GMT 2025 , Edited by admin on Wed Apr 02 05:30:24 GMT 2025
PRIMARY
WIKIPEDIA
Benzodioxolefentanyl
Created by admin on Wed Apr 02 05:30:24 GMT 2025 , Edited by admin on Wed Apr 02 05:30:24 GMT 2025
PRIMARY
EPA CompTox
DTXSID001036791
Created by admin on Wed Apr 02 05:30:24 GMT 2025 , Edited by admin on Wed Apr 02 05:30:24 GMT 2025
PRIMARY
FDA UNII
HK044U64R4
Created by admin on Wed Apr 02 05:30:24 GMT 2025 , Edited by admin on Wed Apr 02 05:30:24 GMT 2025
PRIMARY
CAS
2306823-01-6
Created by admin on Wed Apr 02 05:30:24 GMT 2025 , Edited by admin on Wed Apr 02 05:30:24 GMT 2025
PRIMARY
PUBCHEM
129597846
Created by admin on Wed Apr 02 05:30:24 GMT 2025 , Edited by admin on Wed Apr 02 05:30:24 GMT 2025
PRIMARY
NIH
NCATS
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