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ethyl 2-fluoro-5-hydroxybenzoate

Base Information Edit
  • Chemical Name:ethyl 2-fluoro-5-hydroxybenzoate
  • CAS No.:1214387-36-6
  • Molecular Formula:C9H9FO3
  • Molecular Weight:184.167
  • Hs Code.:2918290090
  • Mol file:1214387-36-6.mol
ethyl 2-fluoro-5-hydroxybenzoate

Synonyms:C9H9FO3

Suppliers and Price of ethyl 2-fluoro-5-hydroxybenzoate
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
  • Crysdot
  • Ethyl2-fluoro-5-hydroxybenzoate 95+%
  • 5g
  • $ 317.00
  • Crysdot
  • Ethyl2-fluoro-5-hydroxybenzoate 95+%
  • 1g
  • $ 119.00
  • Apolloscientific
  • Ethyl2-fluoro-5-hydroxybenzoate 95%
  • 5g
  • $ 445.00
  • Apolloscientific
  • Ethyl2-fluoro-5-hydroxybenzoate 95%
  • 1g
  • $ 150.00
  • AOBChem
  • Ethyl2-fluoro-5-hydroxybenzoate 97%
  • 100g
  • $ 695.00
  • Alichem
  • Ethyl2-fluoro-5-hydroxybenzoate
  • 25g
  • $ 814.06
Total 2 raw suppliers
Chemical Property of ethyl 2-fluoro-5-hydroxybenzoate Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Ethyl2-fluoro-5-hydroxybenzoate 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of ethyl 2-fluoro-5-hydroxybenzoate

There total 2 articles about ethyl 2-fluoro-5-hydroxybenzoate 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 sulfuric acid; at 80 ℃;

Reference yield:

Guidance literature:
With sulfuric acid; Reflux;
Guidance literature:
Multi-step reaction with 3 steps
1.1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 20 °C
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.5 h / Cooling with ice
2.2: 1 h / 20 °C
3.1: sodium hydride / tetrahydrofuran; mineral oil / Cooling with ice
With lithium aluminium tetrahydride; di-isopropyl azodicarboxylate; sodium hydride; triphenylphosphine; In tetrahydrofuran; toluene; mineral oil;
Refernces Edit
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