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Details

Stereochemistry RACEMIC
Molecular Formula C23H28N2O
Molecular Weight 348.4812
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENTRANYL

SMILES

CCC(=O)N(C1CCN(CC1)[C@H]2C[C@@H]2C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=YOKFXXJHMBYPRF-YADHBBJMSA-N
InChI=1S/C23H28N2O/c1-2-23(26)25(19-11-7-4-8-12-19)20-13-15-24(16-14-20)22-17-21(22)18-9-5-3-6-10-18/h3-12,20-22H,2,13-17H2,1H3/t21-,22+/m1/s1

HIDE SMILES / InChI

Molecular Formula C23H28N2O
Molecular Weight 348.4812
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Thu Jul 06 21:04:43 UTC 2023
Edited
by admin
on Thu Jul 06 21:04:43 UTC 2023
Record UNII
K27WI90BWN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENTRANYL
Common Name English
1-(TRANS-2-PHENYLCYCLOPROPYL)-4-(N-PROPIONYLANILINO)PIPERIDINE
Systematic Name English
N-PHENYL-N-(1-(2-PHENYLCYCLOPROPYL)PIPERIDIN-4-YL)PROPANAMIDE
Systematic Name English
PROPANAMIDE, N-PHENYL-N-(1-(2-PHENYLCYCLOPROPYL)-4-PIPERIDINYL)-, TRANS-
Systematic Name English
TRANS-PHENYLCYCLOPROPYL-NORFENTANYL
Common Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Thu Jul 06 21:04:43 UTC 2023 , Edited by admin on Thu Jul 06 21:04:43 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID70907638
Created by admin on Thu Jul 06 21:04:43 UTC 2023 , Edited by admin on Thu Jul 06 21:04:43 UTC 2023
PRIMARY
PUBCHEM
3025333
Created by admin on Thu Jul 06 21:04:43 UTC 2023 , Edited by admin on Thu Jul 06 21:04:43 UTC 2023
PRIMARY N-Phenyl-N-[1-(2-phenylcyclopropyl)piperidin-4-yl]propanamide
CAS
102504-49-4
Created by admin on Thu Jul 06 21:04:43 UTC 2023 , Edited by admin on Thu Jul 06 21:04:43 UTC 2023
PRIMARY
FDA UNII
K27WI90BWN
Created by admin on Thu Jul 06 21:04:43 UTC 2023 , Edited by admin on Thu Jul 06 21:04:43 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY