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4-Chloro-2-ethoxycarbonyl-3,5-Lutidine

Base Information
  • Chemical Name:4-Chloro-2-ethoxycarbonyl-3,5-Lutidine
  • CAS No.:187222-17-9
  • Molecular Formula:C10H12ClNO2
  • Molecular Weight:213.664
  • Hs Code.:
4-Chloro-2-ethoxycarbonyl-3,5-Lutidine

Synonyms:4-Chloro-2-ethoxycarbonyl-3,5-Lutidine

Suppliers and Price of 4-Chloro-2-ethoxycarbonyl-3,5-Lutidine
Supply Marketing:
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
  • Ethyl4-Chloro-3,5-dimethylpicolinate
  • 1g
  • $ 1320.00
Total 2 raw suppliers
Chemical Property of 4-Chloro-2-ethoxycarbonyl-3,5-Lutidine
Chemical Property:
  • Boiling Point:313.4±37.0 °C(Predicted) 
  • Density:1.176±0.06 g/cm3(Predicted) 
Purity/Quality:

95% *data from raw suppliers

Ethyl4-Chloro-3,5-dimethylpicolinate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Ethyl 4-Chloro-3,5-dimethylpicolinate s an intermediate in the synthesis of Omeprazole (O635000), which binds covalently to proton pum, inhibits gastric secreation and is used as an antiulcerative.
Technology Process of 4-Chloro-2-ethoxycarbonyl-3,5-Lutidine

There total 7 articles about 4-Chloro-2-ethoxycarbonyl-3,5-Lutidine 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 trichlorophosphate; at 120 ℃; for 1h;
DOI:10.3987/COM-96-7617
Guidance literature:
With sulfuric acid; dihydrogen peroxide; In 2-oxo-propionic acid ethyl ester; DI-water; toluene;
Guidance literature:
Multi-step reaction with 6 steps
1: 84 percent / anh. potassium carbonate / acetone / 34 h / Heating
2: 20 percent / sodium ethoxide / ethanol / 0.5 h / Heating
3: 92 percent / sulfuric acid / 4 h / Heating
4: 70 percent / p-toluenesulfonic acid monohydrate / toluene / 9 h / Heating
5: 81 percent / hydrogen / 10percent Pd/C / acetic acid / 12 h / 2844.3 Torr / Ambient temperature
6: 88 percent / phosphoryl chloride / 1 h / 120 °C
With sulfuric acid; hydrogen; sodium ethanolate; potassium carbonate; toluene-4-sulfonic acid; trichlorophosphate; palladium on activated charcoal; In ethanol; acetic acid; acetone; toluene;
DOI:10.3987/COM-96-7617
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