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Fluperolone acetate

Base Information
  • Chemical Name:Fluperolone acetate
  • CAS No.:2119-75-7
  • Deprecated CAS:8060-05-7
  • Molecular Formula:C24H31FO6
  • Molecular Weight:434.505
  • Hs Code.:
  • European Community (EC) Number:218-327-4
  • UNII:DOL7Q9DPF9
  • DSSTox Substance ID:DTXSID50895064
  • Nikkaji Number:J7.327J
  • Wikipedia:Fluperolone_acetate
  • Wikidata:Q5462884
  • NCI Thesaurus Code:C169995
  • ChEMBL ID:CHEMBL2107401
  • Mol file:2119-75-7.mol
Fluperolone acetate

Synonyms:fluperolone acetate

Suppliers and Price of Fluperolone acetate
Supply Marketing:
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
  • FluperoloneAcetate
  • 5mg
  • $ 220.00
  • American Custom Chemicals Corporation
  • FLUPEROLONE ACETATE 95.00%
  • 50MG
  • $ 2425.50
  • American Custom Chemicals Corporation
  • FLUPEROLONE ACETATE 95.00%
  • 5MG
  • $ 847.00
Total 7 raw suppliers
Chemical Property of Fluperolone acetate
Chemical Property:
  • Melting Point:251-253° 
  • Boiling Point:580.5°Cat760mmHg 
  • Flash Point:304.9°C 
  • PSA:100.90000 
  • Density:1.3g/cm3 
  • LogP:2.60900 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:4
  • Exact Mass:434.21046687
  • Heavy Atom Count:31
  • Complexity:910
Purity/Quality:

99% *data from raw suppliers

FluperoloneAcetate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C(=O)C1(CCC2C1(CC(C3(C2CCC4=CC(=O)C=CC43C)F)O)C)O)OC(=O)C
  • Isomeric SMILES:C[C@@H](C(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@@H]([C@]3([C@H]2CCC4=CC(=O)C=C[C@@]43C)F)O)C)O)OC(=O)C
  • Uses A corticosteroid with antiinflammatory activity.
Technology Process of Fluperolone acetate

There total 3 articles about Fluperolone acetate 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:
Aus dem 21A-Mesylat (oder Tosylat) u. K-acetat / 200percent;
Guidance literature:
aus 9β.11β-Oxido-17.21a(F)-dihydroxy-21-methyl-pregna-1.4-dien-3.20-dion-21-acetat, HF in THF + Chlf., -70grad;
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