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(3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine

Base Information
  • Chemical Name:(3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine
  • CAS No.:1063733-97-0
  • Molecular Formula:C10H12FNO
  • Molecular Weight:181.21
  • Hs Code.:
  • Mol file:1063733-97-0.mol
(3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine

Synonyms:(3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine

Suppliers and Price of (3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine
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
  • rel-(3R,4S)-4-(4-Fluorophenyl)tetrahydro-3-furanamine
  • 5g
  • $ 7590.00
Total 2 raw suppliers
Chemical Property of (3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine
Chemical Property:
Purity/Quality:

95% *data from raw suppliers

rel-(3R,4S)-4-(4-Fluorophenyl)tetrahydro-3-furanamine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses rel-(3R,4S)-4-(4-Fluorophenyl)tetrahydro-3-furanamine, is a building block used in the synthesis of other chemical compounds, such as Selective Inhibitors of 3-Phosphoinositide-Dependent Kinase (PDK1).
Technology Process of (3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine

There total 6 articles about (3S,4R)-4-(4-fluorophenyl)oxolan-3-aMine 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:
Multi-step reaction with 2 steps
1: chiralpak AD-H / methanol; carbon dioxide / Inert atmosphere
2: hydrogenchloride / Inert atmosphere
With hydrogenchloride; In methanol; carbon dioxide;
DOI:10.1021/jm201019k
Guidance literature:
Multi-step reaction with 2 steps
1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere
2: hydrazine / toluene / 90 °C / Inert atmosphere
With di-isopropyl azodicarboxylate; triphenylphosphine; hydrazine; In tetrahydrofuran; toluene;
DOI:10.1021/jm201019k
upstream raw materials:

4-flourophenylmagnesium bromide

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