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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H28F2N2O.ClH
Molecular Weight 422.939
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-1-(4-fluorophenethyl)-3-methylpiperidin-4-yl)-N-(4-fluorophenyl)propionamide hydrochloride, trans-

SMILES

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

InChI

InChIKey=AZQIIDDZDQQXPK-ZLLYMXMVSA-N
InChI=1S/C23H28F2N2O.ClH/c1-3-23(28)27(21-10-8-20(25)9-11-21)22-13-15-26(16-17(22)2)14-12-18-4-6-19(24)7-5-18;/h4-11,17,22H,3,12-16H2,1-2H3;1H/t17-,22-;/m0./s1

HIDE SMILES / InChI

Molecular Formula C23H28F2N2O
Molecular Weight 386.478
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
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 Wed Apr 02 19:53:05 GMT 2025
Edited
by admin
on Wed Apr 02 19:53:05 GMT 2025
Record UNII
U279N2E8RE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4'-fluoro, para-fluoro (±)-trans-3-methyl Fentanyl hydrochloride
Preferred Name English
N-1-(4-fluorophenethyl)-3-methylpiperidin-4-yl)-N-(4-fluorophenyl)propionamide hydrochloride, trans-
Systematic Name English
Propanamide, N-(4-fluorophenyl)-N-[(3R,4R)-1-[2-(4-fluorophenyl)ethyl]-3-methyl-4-piperidinyl]-, hydrochloride (1:1), rel-
Systematic Name English
trans-N-1-(4-fluorophenethyl)-3-methylpiperidin-4-yl)-N-(4-fluorophenyl)propionamide, monohydrochloride
Systematic Name English
Code System Code Type Description
PUBCHEM
137700376
Created by admin on Wed Apr 02 19:53:05 GMT 2025 , Edited by admin on Wed Apr 02 19:53:05 GMT 2025
PRIMARY
CAS
2748485-38-1
Created by admin on Wed Apr 02 19:53:05 GMT 2025 , Edited by admin on Wed Apr 02 19:53:05 GMT 2025
PRIMARY
FDA UNII
U279N2E8RE
Created by admin on Wed Apr 02 19:53:05 GMT 2025 , Edited by admin on Wed Apr 02 19:53:05 GMT 2025
PRIMARY
CAYMAN
24503
Created by admin on Wed Apr 02 19:53:05 GMT 2025 , Edited by admin on Wed Apr 02 19:53:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID401037139
Created by admin on Wed Apr 02 19:53:05 GMT 2025 , Edited by admin on Wed Apr 02 19:53:05 GMT 2025
PRIMARY