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(S)-tert-butyl-1-(5-fluoropyrimidin-2-yl)ethylcarbamate

Base Information Edit
  • Chemical Name:(S)-tert-butyl-1-(5-fluoropyrimidin-2-yl)ethylcarbamate
  • CAS No.:905587-30-6
  • Molecular Formula:C11H16FN3O2
  • Molecular Weight:241.265
  • Hs Code.:
  • Mol file:905587-30-6.mol
(S)-tert-butyl-1-(5-fluoropyrimidin-2-yl)ethylcarbamate

Synonyms:

Suppliers and Price of (S)-tert-butyl-1-(5-fluoropyrimidin-2-yl)ethylcarbamate
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
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  • price
  • Matrix Scientific
  • (S)-tert-Butyl 1-(5-fluoropyrimidin-2-yl)ethylcarbamate 95%
  • 25g
  • $ 7149.00
  • Matrix Scientific
  • (S)-tert-Butyl 1-(5-fluoropyrimidin-2-yl)ethylcarbamate 95%
  • 5g
  • $ 2383.00
Total 0 raw suppliers
Chemical Property of (S)-tert-butyl-1-(5-fluoropyrimidin-2-yl)ethylcarbamate Edit
Chemical Property:
Purity/Quality:

(S)-tert-Butyl 1-(5-fluoropyrimidin-2-yl)ethylcarbamate 95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
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MSDS Files:
Useful:
Technology Process of (S)-tert-butyl-1-(5-fluoropyrimidin-2-yl)ethylcarbamate

There total 7 articles about (S)-tert-butyl-1-(5-fluoropyrimidin-2-yl)ethylcarbamate 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:
(S)-N-(1-(5-fluoropyrimidin-2-yl)ethyl)acetamide; di-tert-butyl dicarbonate; dmap; In tetrahydrofuran; at 50 ℃; for 40h;
With lithium hydroxide; water; In tetrahydrofuran; at 20 ℃; for 9h;
Guidance literature:
With lithium hydroxide monohydrate; In water; at 20 ℃; for 9h;
DOI:10.1021/jm800343j
Guidance literature:
Multi-step reaction with 3 steps
1.1: tetrahydrofuran; 2-methyltetrahydrofuran / -40 °C
1.2: -25 °C
2.1: (S)-1-phenyl-ethylamine; potassium dihydrogenphosphate; pyridoxal 5'-phosphate; potassium carbonate; acetic acid; ω-transaminase / water; toluene / 18 h / 29 °C / pH 7.5 / Enzymatic reaction
3.1: potassium carbonate / 2-methyltetrahydrofuran; water / 18 h / 40 °C
With potassium dihydrogenphosphate; (S)-1-phenyl-ethylamine; pyridoxal 5'-phosphate; ω-transaminase; potassium carbonate; acetic acid; In tetrahydrofuran; 2-methyltetrahydrofuran; water; toluene; 1.1: |Grignard Reaction;
DOI:10.1021/op400133d
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