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5-chloro-N-(2-ethylphenyl)-2-methoxybenzamide

Base Information Edit
  • Chemical Name:5-chloro-N-(2-ethylphenyl)-2-methoxybenzamide
  • CAS No.:349088-89-7
  • Molecular Formula:C16H16ClNO2
  • Molecular Weight:289.762
  • Hs Code.:
  • Mol file:349088-89-7.mol
5-chloro-N-(2-ethylphenyl)-2-methoxybenzamide

Synonyms:

Suppliers and Price of 5-chloro-N-(2-ethylphenyl)-2-methoxybenzamide
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
  • American Custom Chemicals Corporation
  • 5-CHLORO-N-(2-ETHYLPHENYL)-2-METHOXYBENZAMIDE 95.00%
  • 5MG
  • $ 496.03
Total 0 raw suppliers
Chemical Property of 5-chloro-N-(2-ethylphenyl)-2-methoxybenzamide Edit
Chemical Property:
Purity/Quality:

5-CHLORO-N-(2-ETHYLPHENYL)-2-METHOXYBENZAMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 5-chloro-N-(2-ethylphenyl)-2-methoxybenzamide

There total 5 articles about 5-chloro-N-(2-ethylphenyl)-2-methoxybenzamide 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: thionyl chloride / 3 h / Reflux
2: triethylamine / diethyl ether / 20 °C
With thionyl chloride; triethylamine; In diethyl ether;
DOI:10.1016/j.tet.2016.02.035
Guidance literature:
Multi-step reaction with 3 steps
1: potassium hydroxide / ethylene glycol / 7 h / 170 °C
2: thionyl chloride / 3 h / Reflux
3: triethylamine / diethyl ether / 20 °C
With thionyl chloride; triethylamine; potassium hydroxide; In diethyl ether; ethylene glycol;
DOI:10.1016/j.tet.2016.02.035
Refernces Edit
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