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Brivaracetam (alfaR, 4S)-Isomer

Base Information
  • Chemical Name:Brivaracetam (alfaR, 4S)-Isomer
  • CAS No.:357336-99-3
  • Molecular Formula:C11H20N2O2
  • Molecular Weight:212.29
  • Hs Code.:
Brivaracetam (alfaR, 4S)-Isomer

Synonyms:Brivaracetam (alfaR, 4S)-Isomer;2R-2-[(4S)-2-oxo-4-propylpyrrolidin-1-yl]butanamide

Suppliers and Price of Brivaracetam (alfaR, 4S)-Isomer
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
  • αR,4S-Brivaracetam
  • 25mg
  • $ 2665.00
  • TRC
  • αR,4S-Brivaracetam
  • 10mg
  • $ 1185.00
Total 18 raw suppliers
Chemical Property of Brivaracetam (alfaR, 4S)-Isomer
Chemical Property:
  • Boiling Point:409.3±28.0 °C(Predicted) 
  • PKA:15.74±0.50(Predicted) 
  • PSA:63.40000 
  • Density:1.062±0.06 g/cm3(Predicted) 
  • LogP:1.53710 
  • Storage Temp.:Refrigerator 
  • Solubility.:Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) 
Purity/Quality:

NLT 98% *data from raw suppliers

αR,4S-Brivaracetam *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses αR,4S-Brivaracetam acts as a reagent for the preparation of 2-Oxo-1-pyrrolidine derivatives and their anticonvulsants activity. Also an impurity of Brivaracetam (B677645), a 4-n-propyl analog of levetiracetam (L331500), and a racetam derivative with anticonvulsant properties.
Technology Process of Brivaracetam (alfaR, 4S)-Isomer

There total 202 articles about Brivaracetam (alfaR, 4S)-Isomer 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 (R)-((4,4’-bi-1,3-benzodioxole)-5,5’-diyl)bis(bis(3,5-di-t-butyl-4-methoxyphenyl))phosphine; copper(l) chloride; sodium t-butanolate; In toluene; at -40 ℃; for 24h; Inert atmosphere;
Guidance literature:
With potassium tert-butylate; In tetrahydrofuran;
Guidance literature:
C7H13IO2; With 1,1'-carbonyldiimidazole; In toluene; at 10 - 20 ℃; for 0.166667h; Inert atmosphere;
(S)-2-amino-butanamide; In toluene; at 10 - 20 ℃;
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