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Fenoprofen

Base Information Edit
  • Chemical Name:Fenoprofen
  • CAS No.:31879-05-7
  • Molecular Formula:C15H14O3
  • Molecular Weight:242.27
  • Hs Code.:2918990090
  • Mol file:31879-05-7.mol
Fenoprofen

Synonyms:benzeneacetic acid, α-methyl-3-phenoxy-;2-[3-(phenyloxy)phenyl]propanoic acid;PROGESIC;

Suppliers and Price of Fenoprofen
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
  • FENOPROFEN 95.00%
  • 10G
  • $ 1202.08
  • American Custom Chemicals Corporation
  • FENOPROFEN 95.00%
  • 5G
  • $ 854.74
  • American Custom Chemicals Corporation
  • FENOPROFEN 95.00%
  • 1G
  • $ 228.90
Total 38 raw suppliers
Chemical Property of Fenoprofen Edit
Chemical Property:
  • Melting Point:25°C 
  • Refractive Index:nD25 1.5742 
  • Boiling Point:381.3 °C at 760 mmHg 
  • PKA:4.5(at 25℃) 
  • Flash Point:141.7 °C 
  • PSA:46.53000 
  • Density:1.183 g/cm3 
  • LogP:3.66700 
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform (Slightly), DMSO (Slightly), Methanol (Sparingly) 
  • Water Solubility.:0.1g/L(37 oC) 
Purity/Quality:

98%,99%, *data from raw suppliers

FENOPROFEN 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses antiinflammatory Fenoprofen is used in treating symptoms of rheumatoid arthritis and osteoarthritis; however, fenoprofen exhibits a number of undesirable side effects.
  • Indications Fenoprofen (Nalfon) is chemically and pharmacologically similar to ibuprofen and is used in the treatment of rheumatoid arthritis, osteoarthritis, and mild to moderate pain. GI effects such as dyspepsia and pain are most common, although dizziness, pruritus, and palpitations may occur. GI bleeding, sometimes severe, has been reported, and interstitial nephritis has been rarely associated with this drug. Concomitant administration of aspirin decreases the biological half-life of fenoprofen by increasing the metabolic clearance of hydroxylated fenoprofen. Chronic administration of phenobarbital also decreases the drug’s half-life.
  • Therapeutic Function Antiinflammatory
  • Clinical Use Clinical use NSAID and analgesic
  • Drug interactions Potentially hazardous interactions with other drugs ACE inhibitors and angiotensin-II antagonists: increased risk of hyperkalaemia and nephrotoxicity; reduced hypotensive effect. Analgesics: avoid concomitant use with other NSAIDs or aspirin; avoid concomitant use with ketorolac (increased side effects and haemorrhage). Antibacterials: possibly increased risk of convulsions with quinolones. Anticoagulants: effects of coumarins and phenindione enhanced; possibly increased risk of bleeding with heparin, dabigatran and edoxaban - avoid long term use with edoxaban. Antidepressants: increased risk of bleeding with SSRIs or venlafaxine. Antidiabetics: effects of sulphonylureas enhanced. Antiepileptics: possibly enhanced effect of phenytoin. Antivirals: concentration possibly increased by ritonavir; increased risk of haematological toxicity with zidovudine. Ciclosporin: may potentiate nephrotoxicity. Cytotoxics: reduced excretion of methotrexate; increased risk of bleeding with erlotinib. Diuretics: increased risk of nephrotoxicity; antagonism of diuretic effect; hyperkalaemia with potassium-sparing diuretics. Lithium: excretion reduced. Pentoxifylline: increased risk of bleeding. Tacrolimus: increased risk of nephrotoxicity
Technology Process of Fenoprofen

There total 75 articles about Fenoprofen 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:
In tetrahydrofuran; ethanol; water; tert-butyl alcohol;
Guidance literature:
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; sodium chlorite; In water; acetonitrile; at 35 ℃; for 24h; aq. phosphate buffer;
DOI:10.1055/s-0030-1258580
Guidance literature:
3-bromodiphenyl ether; With zinc(II) fluoride; tri-tert-butyl phosphine; bis(dibenzylideneacetone)-palladium(0); In toluene; for 0.666667h; Inert atmosphere;
1,1-bis(trimethylsilyloxy)prop-1-ene; In tetrahydrofuran; N,N-dimethyl-formamide; toluene; at 80 ℃; for 12h; Sealed tube; Inert atmosphere;
DOI:10.1021/jacs.9b03291
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