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5-TRANS FLUPROSTENOL

Base Information
  • Chemical Name:5-TRANS FLUPROSTENOL
  • CAS No.:57968-83-9
  • Molecular Formula:C23H29F3O6
  • Molecular Weight:458.475
  • Hs Code.:
  • Mol file:57968-83-9.mol
5-TRANS FLUPROSTENOL

Synonyms:(5E)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)-phenoxy]-1-butenyl]cyclopentyl]-5-heptenoic acid

Suppliers and Price of 5-TRANS FLUPROSTENOL
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
  • Cayman Chemical
  • 5-trans Fluprostenol ≥95%
  • 5mg
  • $ 341.00
  • Cayman Chemical
  • 5-trans Fluprostenol ≥95%
  • 1mg
  • $ 77.00
  • Cayman Chemical
  • 5-trans Fluprostenol ≥95%
  • 10mg
  • $ 605.00
  • AK Scientific
  • 5-TransFluprostenol
  • 5mg
  • $ 525.00
Total 7 raw suppliers
Chemical Property of 5-TRANS FLUPROSTENOL
Chemical Property:
Purity/Quality:

95% *data from raw suppliers

5-trans Fluprostenol ≥95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 5-TRANS FLUPROSTENOL

There total 3 articles about 5-TRANS FLUPROSTENOL 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:
2,2-bis(hydroxymethyl)propyl 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-[3-(trifluoromethyl)-phenoxy]-1-butenyl]cyclopentyl]-5-heptenate; With lithium hydroxide monohydrate; In methanol;
With citric acid; In water; pH=4 - 5; Overall yield = ~ 98 %; Overall yield = 1.43 g;
DOI:10.1016/j.tet.2012.11.087
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