C₁₆H₁₆N₂O₅

Base Information

Chemical Name:C₁₆H₁₆N₂O₅
CAS No.:475479-10-8
Molecular Formula:C₁₆H₁₆N₂O₅
Molecular Weight:316.313
Hs Code.:

C<sub>16</sub>H<sub>16</sub>N<sub>2</sub>O<sub>5</sub>

Synonyms:

Suppliers and Price of C₁₆H₁₆N₂O₅

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
(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 1 raw suppliers

Chemical Property of C₁₆H₁₆N₂O₅

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:

Reference yield: 83.0%

: 383428-73-7
3-((α)‐2‐(2‐(6‐chloropyrimidin-4‐yl)oxy)phenyl)methyl-3-methoxyacrylate

: 124-41-4
sodium methylate

: 475479-10-8
C₁₆H₁₆N₂O₅

Guidance literature:: In methanol; Reflux;

Reference yield: 69.0%

: 67-56-1
methanol

: 131860-97-4
(E)-methyl 2-[2-(6-chloropyrimidin-4-yloxy)phenyl]-3-methoxy-propenoate

: 475479-10-8
C₁₆H₁₆N₂O₅

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

Reference yield:

: 175971-61-6
2-(2-hydroxyphenyl)-3,3-dimethoxypropionic acid methyl ester

: 475479-10-8
C₁₆H₁₆N₂O₅

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