U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C24H32N2O
Molecular Weight 364.5237
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of .ALPHA.-METHYL-BUTYRFENTANYL

SMILES

CCCC(=O)N(C1CCN(CC1)C(C)CC2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=IPIGJTVNMCMXMT-UHFFFAOYSA-N
InChI=1S/C24H32N2O/c1-3-10-24(27)26(22-13-8-5-9-14-22)23-15-17-25(18-16-23)20(2)19-21-11-6-4-7-12-21/h4-9,11-14,20,23H,3,10,15-19H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C24H32N2O
Molecular Weight 364.5237
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Thu Jul 06 20:59:53 UTC 2023
Edited
by admin
on Thu Jul 06 20:59:53 UTC 2023
Record UNII
0N39CAW66T
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
.ALPHA.-METHYL-BUTYRFENTANYL
Common Name English
ALPHAMETHYLBUTYRLFENTANYL
Common Name English
N-(1-(1-METHYL-2-PHENYL-ETHYL)-4-PIPERIDYL)-N-PHENYL-BUTANAMIDE
Systematic Name English
BUTANAMIDE, N-(1-(1-METHYL-2-PHENYLETHYL)-4-PIPERIDINYL)-N-PHENYL-
Systematic Name English
.ALPHA.-METHYL BUTYRYL FENTANYL
Common Name English
.ALPHA.-METHYLBUTYRFENTANYL
Common Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Thu Jul 06 20:59:53 UTC 2023 , Edited by admin on Thu Jul 06 20:59:53 UTC 2023
Code System Code Type Description
FDA UNII
0N39CAW66T
Created by admin on Thu Jul 06 20:59:53 UTC 2023 , Edited by admin on Thu Jul 06 20:59:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID001036765
Created by admin on Thu Jul 06 20:59:53 UTC 2023 , Edited by admin on Thu Jul 06 20:59:53 UTC 2023
PRIMARY
MANUFACTURER PRODUCT INFORMATION
.ALPHA.-METHYL BUTYRYL FENTANYL
Created by admin on Thu Jul 06 20:59:53 UTC 2023 , Edited by admin on Thu Jul 06 20:59:53 UTC 2023
PRIMARY
CAS
244195-36-6
Created by admin on Thu Jul 06 20:59:53 UTC 2023 , Edited by admin on Thu Jul 06 20:59:53 UTC 2023
PRIMARY
PUBCHEM
527016
Created by admin on Thu Jul 06 20:59:53 UTC 2023 , Edited by admin on Thu Jul 06 20:59:53 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY