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C16H16N2O5

Base Information Edit
  • Chemical Name:C16H16N2O5
  • CAS No.:475479-10-8
  • Molecular Formula:C16H16N2O5
  • Molecular Weight:316.313
  • Hs Code.:
  • Mol file:475479-10-8.mol
C<sub>16</sub>H<sub>16</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:

Suppliers and Price of C16H16N2O5
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
  • (E)-Methyl3-methoxy-2-(2-((6-methoxypyrimidin-4-yl)oxy)phenyl)acrylate
  • 25mg
  • $ 875.00
  • Crysdot
  • (E)-Methyl3-methoxy-2-(2-((6-methoxypyrimidin-4-yl)oxy)phenyl)acrylate 95+%
  • 1g
  • $ 947.00
  • Chemenu
  • methyl(E)-3-methoxy-2-(2-((6-methoxypyrimidin-4-yl)oxy)phenyl)acrylate 95%
  • 1g
  • $ 893.00
  • American Custom Chemicals Corporation
  • (E)-METHYL 3-METHOXY-2-(2-((6-METHOXYPYRIMIDIN-4-YL)OXY)PHENYL)ACRYLATE 95.00%
  • 5MG
  • $ 498.27
  • Alichem
  • (E)-Methyl3-methoxy-2-(2-((6-methoxypyrimidin-4-yl)oxy)phenyl)acrylate
  • 1g
  • $ 791.04
Total 0 raw suppliers
Chemical Property of C16H16N2O5 Edit
Chemical Property:
Purity/Quality:

(E)-Methyl3-methoxy-2-(2-((6-methoxypyrimidin-4-yl)oxy)phenyl)acrylate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (E)-Methyl 3-methoxy-2-(2-((6-methoxypyrimidin-4-yl)oxy)phenyl)acrylate is an intermediate used in the preparation of β-methoxyacrylate analogs with antifungal activity.
Technology Process of C16H16N2O5

There total 10 articles about C16H16N2O5 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 1,4-diaza-bicyclo[2.2.2]octane; potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 2h; Inert atmosphere;
DOI:10.1002/jccs.201200295
Guidance literature:
Multi-step reaction with 3 steps
1: potassium carbonate / N,N-dimethyl-formamide / 8 h / 60 °C
2: methanesulfonic acid / acetic anhydride / 2 h / 90 °C
3: potassium carbonate; 1,4-diaza-bicyclo[2.2.2]octane / N,N-dimethyl-formamide / 2 h / 80 °C / Inert atmosphere
With 1,4-diaza-bicyclo[2.2.2]octane; methanesulfonic acid; potassium carbonate; In acetic anhydride; N,N-dimethyl-formamide;
DOI:10.1002/jccs.201200295
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