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α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid

Base Information Edit
  • Chemical Name:α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid
  • CAS No.:253324-75-3
  • Molecular Formula:C13H15F2NO4
  • Molecular Weight:287.263
  • Hs Code.:
  • Mol file:253324-75-3.mol
α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid

Synonyms:α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid

Suppliers and Price of α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 2 raw suppliers
Chemical Property of α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
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Technology Process of α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid

There total 5 articles about α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid 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:
α-(((1,1,-dimethylethoxy)carbonyl)amino)-3,5-difluorobenzeneacetic acid methyl ester; With water; lithium hydroxide; In tetrahydrofuran; methanol; at 0 - 20 ℃; for 3h;
With sodium hydrogen sulfate; In water; ethyl acetate;
Guidance literature:
Multi-step reaction with 2 steps
1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 18 h / 2585.81 Torr
2: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 0 - 20 °C
With water; hydrogen; lithium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethyl acetate;
Guidance literature:
Multi-step reaction with 4 steps
1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 18 h / Inert atmosphere; Reflux
2: sodium azide / acetonitrile / 20.5 h / 20 °C / Inert atmosphere
3: hydrogen / palladium 10% on activated carbon / ethyl acetate / 18 h / 2585.81 Torr
4: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 0 - 20 °C
With N-Bromosuccinimide; sodium azide; 2,2'-azobis(isobutyronitrile); water; hydrogen; lithium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; tetrachloromethane; ethyl acetate; acetonitrile;
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