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Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)-

Base Information Edit
  • Chemical Name:Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)-
  • CAS No.:209982-91-2
  • Molecular Formula:C8H6F2O3
  • Molecular Weight:188.131
  • Hs Code.:
  • Mol file:209982-91-2.mol
Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)-

Synonyms:S-(+)-3,5-difluoromandelic acid

Suppliers and Price of Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)-
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
  • ChemScene
  • Benzeneaceticacid,3,5-difluoro-α-hydroxy-,(αS)- >97.0%
  • 100mg
  • $ 218.00
  • AK Scientific
  • Benzeneaceticacid,3,5-difluoro--hydroxy-,(S)-
  • 100mg
  • $ 356.00
Total 4 raw suppliers
Chemical Property of Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)- Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Benzeneaceticacid,3,5-difluoro-α-hydroxy-,(αS)- >97.0% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)-

There total 2 articles about Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)- 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 lithium hydroxide; In aqueous THF;
Guidance literature:
With D-lactate oxidase from Gluconobacter oxydans 621H; oxygen; catalase; In aq. buffer; at 30 ℃; for 12h; pH=7.4; Reagent/catalyst; enantioselective reaction; Resolution of racemate; Enzymatic reaction;
DOI:10.1002/cctc.201600536
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