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ethyl 2-bromo-2-(3-(trifluoromethyl)phenyl)propanoate

Base Information Edit
  • Chemical Name:ethyl 2-bromo-2-(3-(trifluoromethyl)phenyl)propanoate
  • CAS No.:1141713-87-2
  • Molecular Formula:C12H12BrF3O2
  • Molecular Weight:325.125
  • Hs Code.:
  • Mol file:1141713-87-2.mol
ethyl 2-bromo-2-(3-(trifluoromethyl)phenyl)propanoate

Synonyms:ethyl 2-bromo-2-(3-(trifluoromethyl)phenyl)propanoate

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Chemical Property of ethyl 2-bromo-2-(3-(trifluoromethyl)phenyl)propanoate Edit
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Technology Process of ethyl 2-bromo-2-(3-(trifluoromethyl)phenyl)propanoate

There total 2 articles about ethyl 2-bromo-2-(3-(trifluoromethyl)phenyl)propanoate 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:
ethyl 2-(3-(trifluoromethyl)phenyl)propionate; With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at -78 ℃; Inert atmosphere;
With chloro-trimethyl-silane; In tetrahydrofuran; hexane; at 20 ℃; for 2h; Inert atmosphere;
With N-Bromosuccinimide; In tetrahydrofuran; hexane; at -78 - 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/jacs.7b05468
Guidance literature:
Multi-step reaction with 2 steps
1.1: toluene-4-sulfonic acid; [bis(acetoxy)iodo]benzene
2.1: diisopropylamine; n-butyllithium / tetrahydrofuran; hexane / -78 °C / Inert atmosphere
2.2: 2 h / 20 °C / Inert atmosphere
2.3: 2 h / -78 - 20 °C / Inert atmosphere
With n-butyllithium; [bis(acetoxy)iodo]benzene; toluene-4-sulfonic acid; diisopropylamine; In tetrahydrofuran; hexane;
DOI:10.1021/jacs.7b05468
Guidance literature:
With D-glucose; glucose dehydrogenase GDH-105; gluconobacter oxydans enoate reductase (GluER), mutant Y177F; nicotinamide adenine dinucleotide phosphate; In isopropyl alcohol; at 25 ℃; for 24h; pH=8; Overall yield = 75 %; enantioselective reaction; Inert atmosphere; Sealed tube; Enzymatic reaction;
DOI:10.1021/jacs.7b05468
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