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2-AMINO-1-(4-TRIFLUOROMETHYL-PHENYL)-ETHANOL HCL

Base Information Edit
  • Chemical Name:2-AMINO-1-(4-TRIFLUOROMETHYL-PHENYL)-ETHANOL HCL
  • CAS No.:852392-18-8
  • Molecular Formula:C9H10F3NO2
  • Molecular Weight:221.179
  • Hs Code.:2922500090
  • Mol file:852392-18-8.mol
2-AMINO-1-(4-TRIFLUOROMETHYL-PHENYL)-ETHANOL HCL

Synonyms:2-amino-1-(3-trifluoromethoxy-phenyl)-ethanol

Suppliers and Price of 2-AMINO-1-(4-TRIFLUOROMETHYL-PHENYL)-ETHANOL HCL
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
  • Packaging
  • price
  • TRC
  • α-(Aminomethyl)-3-(trifluoromethoxy)benzenemethanol
  • 100mg
  • $ 185.00
  • Chemenu
  • 2-Amino-1-[3-(trifluoromethoxy)phenyl]ethanol 95%
  • 5g
  • $ 1850.00
  • Chemenu
  • 2-Amino-1-[3-(trifluoromethoxy)phenyl]ethanol 95%
  • 1g
  • $ 770.00
  • American Custom Chemicals Corporation
  • ALPHA-(AMINOMETHYL)-3-(TRIFLUOROMETHOXY)-BENZENEMETHANOL 95.00%
  • 5MG
  • $ 505.23
Total 2 raw suppliers
Chemical Property of 2-AMINO-1-(4-TRIFLUOROMETHYL-PHENYL)-ETHANOL HCL Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

α-(Aminomethyl)-3-(trifluoromethoxy)benzenemethanol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses α-(Aminomethyl)-3-(trifluoromethoxy)benzenemethanol is used as a reagent in the synthesis of potent and selective ethanolamine inhibitors of bacterial phenylalanyl tRNA synthetase. It is also used as a reagent in the synthesis of 1-aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase.
Technology Process of 2-AMINO-1-(4-TRIFLUOROMETHYL-PHENYL)-ETHANOL HCL

There total 2 articles about 2-AMINO-1-(4-TRIFLUOROMETHYL-PHENYL)-ETHANOL HCL 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:
Multi-step reaction with 2 steps
1: ZnI2 / diethyl ether
2: LiAlH4 / diethyl ether / Heating
With lithium aluminium tetrahydride; zinc(II) iodide; In diethyl ether;
DOI:10.1016/j.bmcl.2005.03.003
Guidance literature:
With lithium aluminium tetrahydride; In diethyl ether; Heating;
DOI:10.1016/j.bmcl.2005.03.003
Guidance literature:
2-amino-1-(3-trifluoromethoxy-phenyl)-ethanol; 4-chloro-6-(3-chloro-4-trifluoromethylphenyl)-pyrimidine; With N-ethyl-N,N-diisopropylamine; In butan-1-ol; at 100 ℃; for 20h; Inert atmosphere;
trifluoroacetic acid; In water; acetonitrile;
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