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Base Information Edit
  • Chemical Name:Norfenfluramine
  • CAS No.:1886-26-6
  • Molecular Formula:C10H12F3N
  • Molecular Weight:203.207
  • Hs Code.:2921499090
  • NSC Number:43036
  • UNII:037A9J3PSW
  • DSSTox Substance ID:DTXSID60904717
  • Nikkaji Number:J50.067D
  • Wikipedia:Norfenfluramine
  • Wikidata:Q3069482
  • Pharos Ligand ID:B5JX9WZ82R6K
  • ChEMBL ID:CHEMBL1979333
  • Mol file:1886-26-6.mol


Suppliers and Price of Norfenfluramine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • DesethylFenfluramine
  • 100mg
  • $ 220.00
  • American Custom Chemicals Corporation
  • (+/-)-NORFENFLURAMINE 95.00%
  • 5MG
  • $ 499.82
Total 9 raw suppliers
Chemical Property of Norfenfluramine Edit
Chemical Property:
  • Vapor Pressure:0.15mmHg at 25°C 
  • Refractive Index:1.466 
  • Boiling Point:215.2 °C at 760 mmHg 
  • Flash Point:88.9 °C 
  • PSA:26.02000 
  • Density:1.152 g/cm3 
  • LogP:3.29540 
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:203.09218387
  • Heavy Atom Count:14
  • Complexity:179

99%, *data from raw suppliers

DesethylFenfluramine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

  • Canonical SMILES:CC(CC1=CC(=CC=C1)C(F)(F)F)N
Technology Process of Norfenfluramine

There total 4 articles about Norfenfluramine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
1-[(3′-trifluoromethyl)phenyl]-2-propanol; With sodium hypochlorite; 2-azaadamantane-N-oxyl; In water; for 1h; pH=8.9;
With pyridoxal 5'-phosphate; isopropylamine; In aq. phosphate buffer; at 30 ℃; for 24h; pH=7.5; stereoselective reaction;
Guidance literature:
With lithium aluminium tetrahydride;
Guidance literature:
Multi-step reaction with 2 steps
1: nBuNH2
2: LiAlH4
With lithium aluminium tetrahydride; N-butylamine;
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