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Fluradoline

Base Information Edit
  • Chemical Name:Fluradoline
  • CAS No.:71316-84-2
  • Molecular Formula:C17H16FNOS
  • Molecular Weight:301.385
  • Hs Code.:
  • UNII:WEP02A9K8C
  • Nikkaji Number:J32.880D
  • Wikidata:Q27292591
  • NCI Thesaurus Code:C83803
  • ChEMBL ID:CHEMBL357858
  • Mol file:71316-84-2.mol
Fluradoline

Synonyms:fluradoline;fluradoline hydrochloride;fluradoline maleate (1:1) salt;HP 494;HP-494

Suppliers and Price of Fluradoline
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
  • American Custom Chemicals Corporation
  • FLURADOLINE 95.00%
  • 5MG
  • $ 495.44
Total 4 raw suppliers
Chemical Property of Fluradoline Edit
Chemical Property:
  • Vapor Pressure:3.35E-08mmHg at 25°C 
  • Boiling Point:447.5°C at 760 mmHg 
  • Flash Point:224.4°C 
  • PSA:46.56000 
  • Density:1.26g/cm3 
  • LogP:4.77300 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:301.09366347
  • Heavy Atom Count:21
  • Complexity:376
Purity/Quality:

97% *data from raw suppliers

FLURADOLINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CNCCSC1=CC2=CC=CC=C2OC3=C1C=C(C=C3)F
  • Uses Analgesic.
Technology Process of Fluradoline

There total 6 articles about Fluradoline 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:
With potassium hydroxide; In ethylene glycol; at 150 - 160 ℃; for 1h;
DOI:10.1021/jm00179a005
Guidance literature:
Multi-step reaction with 6 steps
1: 90 percent / KOH / ethanol; H2O / 3 h / Heating
2: thionyl chloride / 0.17 h / Heating
3: 80 percent / AlCl3 / 1,2-dichloro-ethane / 2 h / Heating
4: boron trifluoride / acetic acid / 1.) RT, 16 h, 2.) reflux, 30 min
5: 72 percent / K2CO3 / CH2Cl2 / 24 h / Ambient temperature
6: KOH / ethane-1,2-diol / 1 h / 150 - 160 °C
With potassium hydroxide; aluminium trichloride; thionyl chloride; boron trifluoride; potassium carbonate; In ethanol; dichloromethane; water; ethylene glycol; acetic acid; 1,2-dichloro-ethane;
DOI:10.1021/jm00179a005
Guidance literature:
Multi-step reaction with 3 steps
1: boron trifluoride / acetic acid / 1.) RT, 16 h, 2.) reflux, 30 min
2: 72 percent / K2CO3 / CH2Cl2 / 24 h / Ambient temperature
3: KOH / ethane-1,2-diol / 1 h / 150 - 160 °C
With potassium hydroxide; boron trifluoride; potassium carbonate; In dichloromethane; ethylene glycol; acetic acid;
DOI:10.1021/jm00179a005
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