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Details

Stereochemistry ACHIRAL
Molecular Formula C27H36N2O
Molecular Weight 404.5875
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TETRAMETHYLCYCLOPROPYLFENTANYL

SMILES

CC1(C)C(C(=O)N(C2CCN(CCC3=CC=CC=C3)CC2)C4=CC=CC=C4)C1(C)C

InChI

InChIKey=BYCDHAVFKDTVAM-UHFFFAOYSA-N
InChI=1S/C27H36N2O/c1-26(2)24(27(26,3)4)25(30)29(22-13-9-6-10-14-22)23-16-19-28(20-17-23)18-15-21-11-7-5-8-12-21/h5-14,23-24H,15-20H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C27H36N2O
Molecular Weight 404.5875
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Thu Jul 06 21:11:59 UTC 2023
Edited
by admin
on Thu Jul 06 21:11:59 UTC 2023
Record UNII
0WGC89YK4R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TETRAMETHYLCYCLOPROPYLFENTANYL
Common Name English
2,2,3,3-TETRAMETHYL-N-(1-PHENETHYLPIPERIDIN-4-YL)-N-PHENYLCYCLOPROPANE-1-CARBOXAMIDE
Systematic Name English
CYCLOPROPANECARBOXAMIDE, 2,2,3,3-TETRAMETHYL-N-PHENYL-N-(1-(2-PHENYLETHYL)-4-PIPERIDINYL)-
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Thu Jul 06 21:11:59 UTC 2023 , Edited by admin on Thu Jul 06 21:11:59 UTC 2023
Code System Code Type Description
WIKIPEDIA
Tetramethylcyclopropylfentanyl
Created by admin on Thu Jul 06 21:11:59 UTC 2023 , Edited by admin on Thu Jul 06 21:11:59 UTC 2023
PRIMARY
EPA CompTox
DTXSID001036810
Created by admin on Thu Jul 06 21:11:59 UTC 2023 , Edited by admin on Thu Jul 06 21:11:59 UTC 2023
PRIMARY
PUBCHEM
137700015
Created by admin on Thu Jul 06 21:11:59 UTC 2023 , Edited by admin on Thu Jul 06 21:11:59 UTC 2023
PRIMARY
FDA UNII
0WGC89YK4R
Created by admin on Thu Jul 06 21:11:59 UTC 2023 , Edited by admin on Thu Jul 06 21:11:59 UTC 2023
PRIMARY
CAS
2309383-11-5
Created by admin on Thu Jul 06 21:11:59 UTC 2023 , Edited by admin on Thu Jul 06 21:11:59 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY