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(2R)-2-bromo-Butanoic acid methyl ester

Base Information
  • Chemical Name:(2R)-2-bromo-Butanoic acid methyl ester
  • CAS No.:114438-75-4
  • Molecular Formula:C5H9BrO2
  • Molecular Weight:181.029
  • Hs Code.:
  • Mol file:114438-75-4.mol
(2R)-2-bromo-Butanoic acid methyl ester

Synonyms:

Suppliers and Price of (2R)-2-bromo-Butanoic acid methyl ester
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
  • Ambeed
  • Methyl(R)-2-bromobutanoate 98%
  • 25g
  • $ 336.00
  • Ambeed
  • Methyl(R)-2-bromobutanoate 98%
  • 5g
  • $ 107.00
  • Ambeed
  • Methyl(R)-2-bromobutanoate 98%
  • 1g
  • $ 33.00
  • Ambeed
  • Methyl(R)-2-bromobutanoate 98%
  • 250mg
  • $ 14.00
Total 8 raw suppliers
Chemical Property of (2R)-2-bromo-Butanoic acid methyl ester
Chemical Property:
  • Boiling Point:171.0±0.0 °C(Predicted) 
  • PSA:0.00000 
  • Density:1.413±0.06 g/cm3(Predicted) 
  • LogP:0.00000 
Purity/Quality:

99.0% *data from raw suppliers

Methyl(R)-2-bromobutanoate 98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (2R)-2-bromo-Butanoic acid methyl ester

There total 5 articles about (2R)-2-bromo-Butanoic acid methyl ester 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 D-glucose; enoate reductase old yellow enzyme 2 from S. cerevisiae; GDH from B. megaterium; nicotinamide adenine dinucleotide phosphate; In N,N-dimethyl-formamide; at 30 ℃; for 24h; pH=7; optical yield given as %ee; enantioselective reaction; aq. phosphate buffer; Enzymatic reaction;
DOI:10.1021/op200086t
Guidance literature:
With Sphingobium japonicum haloalkane dehalogenase; at 21 ℃; pH=8.2; optical yield given as %ee; enantioselective reaction; Tris sulfate buffer; Resolution of racemate; Enzymatic reaction;
DOI:10.1002/anie.201001753
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