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Details

Stereochemistry ACHIRAL
Molecular Formula C25H28N2O3
Molecular Weight 404.5014
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ortho-methoxy Furanyl fentanyl

SMILES

COC1=CC=CC=C1N(C2CCN(CCC3=CC=CC=C3)CC2)C(=O)C4=CC=CO4

InChI

InChIKey=DCDCWVRDPIOMBB-UHFFFAOYSA-N
InChI=1S/C25H28N2O3/c1-29-23-11-6-5-10-22(23)27(25(28)24-12-7-19-30-24)21-14-17-26(18-15-21)16-13-20-8-3-2-4-9-20/h2-12,19,21H,13-18H2,1H3

HIDE SMILES / InChI

Molecular Formula C25H28N2O3
Molecular Weight 404.5014
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 05:28:41 GMT 2025
Edited
by admin
on Wed Apr 02 05:28:41 GMT 2025
Record UNII
ND9OR22OK0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ORTHO-METHOXYFURANYLFENTANYL
Preferred Name English
ortho-methoxy Furanyl fentanyl
Common Name English
N-(2-Methoxyphenyl)-N-[1-(2-phenylethyl)-4-piperidinyl]-2-furancarboxamide
Systematic Name English
2-Furancarboxamide, N-(2-methoxyphenyl)-N-[1-(2-phenylethyl)-4-piperidinyl]-
Common Name English
N-(1-PHENETHYLPIPERIDIN-4-YL)-N-(2-METHOXYPHENYL)FURAN-2-CARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Wed Apr 02 05:28:41 GMT 2025 , Edited by admin on Wed Apr 02 05:28:41 GMT 2025
Code System Code Type Description
CAYMAN
22805
Created by admin on Wed Apr 02 05:28:41 GMT 2025 , Edited by admin on Wed Apr 02 05:28:41 GMT 2025
PRIMARY
CAS
101343-50-4
Created by admin on Wed Apr 02 05:28:41 GMT 2025 , Edited by admin on Wed Apr 02 05:28:41 GMT 2025
PRIMARY
FDA UNII
ND9OR22OK0
Created by admin on Wed Apr 02 05:28:41 GMT 2025 , Edited by admin on Wed Apr 02 05:28:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID901037241
Created by admin on Wed Apr 02 05:28:41 GMT 2025 , Edited by admin on Wed Apr 02 05:28:41 GMT 2025
PRIMARY
PUBCHEM
13653667
Created by admin on Wed Apr 02 05:28:41 GMT 2025 , Edited by admin on Wed Apr 02 05:28:41 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> AGONIST
Related Record Type Details
ACTIVE MOIETY